US20050158499A1 - Port tube and closure composition, structure and assembly for a flowale material container - Google Patents

Port tube and closure composition, structure and assembly for a flowale material container Download PDF

Info

Publication number
US20050158499A1
US20050158499A1 US11/079,767 US7976705A US2005158499A1 US 20050158499 A1 US20050158499 A1 US 20050158499A1 US 7976705 A US7976705 A US 7976705A US 2005158499 A1 US2005158499 A1 US 2005158499A1
Authority
US
United States
Prior art keywords
ethylene
assembly
layer
weight
copolymer
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Abandoned
Application number
US11/079,767
Inventor
Michael Ling
William Hurst
Lecon Woo
Algirdas Bindokas
Patrick Ryan
Scott Edwards
Henk Blom
Atul Khare
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Individual
Original Assignee
Individual
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Individual filed Critical Individual
Priority to US11/079,767 priority Critical patent/US20050158499A1/en
Publication of US20050158499A1 publication Critical patent/US20050158499A1/en
Abandoned legal-status Critical Current

Links

Images

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L23/00Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
    • C08L23/02Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
    • C08L23/10Homopolymers or copolymers of propene
    • C08L23/12Polypropene
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61LMETHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
    • A61L29/00Materials for catheters, medical tubing, cannulae, or endoscopes or for coating catheters
    • A61L29/12Composite materials, i.e. containing one material dispersed in a matrix of the same or different material
    • A61L29/126Composite materials, i.e. containing one material dispersed in a matrix of the same or different material having a macromolecular matrix
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C66/00General aspects of processes or apparatus for joining preformed parts
    • B29C66/01General aspects dealing with the joint area or with the area to be joined
    • B29C66/05Particular design of joint configurations
    • B29C66/10Particular design of joint configurations particular design of the joint cross-sections
    • B29C66/11Joint cross-sections comprising a single joint-segment, i.e. one of the parts to be joined comprising a single joint-segment in the joint cross-section
    • B29C66/112Single lapped joints
    • B29C66/1122Single lap to lap joints, i.e. overlap joints
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C66/00General aspects of processes or apparatus for joining preformed parts
    • B29C66/50General aspects of joining tubular articles; General aspects of joining long products, i.e. bars or profiled elements; General aspects of joining single elements to tubular articles, hollow articles or bars; General aspects of joining several hollow-preforms to form hollow or tubular articles
    • B29C66/51Joining tubular articles, profiled elements or bars; Joining single elements to tubular articles, hollow articles or bars; Joining several hollow-preforms to form hollow or tubular articles
    • B29C66/53Joining single elements to tubular articles, hollow articles or bars
    • B29C66/532Joining single elements to the wall of tubular articles, hollow articles or bars
    • B29C66/5326Joining single elements to the wall of tubular articles, hollow articles or bars said single elements being substantially flat
    • B29C66/53261Enclosing tubular articles between substantially flat elements
    • B29C66/53262Enclosing spouts between the walls of bags, e.g. of medical bags
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C66/00General aspects of processes or apparatus for joining preformed parts
    • B29C66/70General aspects of processes or apparatus for joining preformed parts characterised by the composition, physical properties or the structure of the material of the parts to be joined; Joining with non-plastics material
    • B29C66/71General aspects of processes or apparatus for joining preformed parts characterised by the composition, physical properties or the structure of the material of the parts to be joined; Joining with non-plastics material characterised by the composition of the plastics material of the parts to be joined
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C66/00General aspects of processes or apparatus for joining preformed parts
    • B29C66/70General aspects of processes or apparatus for joining preformed parts characterised by the composition, physical properties or the structure of the material of the parts to be joined; Joining with non-plastics material
    • B29C66/72General aspects of processes or apparatus for joining preformed parts characterised by the composition, physical properties or the structure of the material of the parts to be joined; Joining with non-plastics material characterised by the structure of the material of the parts to be joined
    • B29C66/723General aspects of processes or apparatus for joining preformed parts characterised by the composition, physical properties or the structure of the material of the parts to be joined; Joining with non-plastics material characterised by the structure of the material of the parts to be joined being multi-layered
    • B29C66/7234General aspects of processes or apparatus for joining preformed parts characterised by the composition, physical properties or the structure of the material of the parts to be joined; Joining with non-plastics material characterised by the structure of the material of the parts to be joined being multi-layered comprising a barrier layer
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B1/00Layered products having a general shape other than plane
    • B32B1/08Tubular products
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B27/00Layered products comprising a layer of synthetic resin
    • B32B27/06Layered products comprising a layer of synthetic resin as the main or only constituent of a layer, which is next to another layer of the same or of a different material
    • B32B27/08Layered products comprising a layer of synthetic resin as the main or only constituent of a layer, which is next to another layer of the same or of a different material of synthetic resin
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B27/00Layered products comprising a layer of synthetic resin
    • B32B27/32Layered products comprising a layer of synthetic resin comprising polyolefins
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L23/00Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
    • C08L23/02Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
    • C08L23/04Homopolymers or copolymers of ethene
    • C08L23/08Copolymers of ethene
    • C08L23/0807Copolymers of ethene with unsaturated hydrocarbons only containing more than three carbon atoms
    • C08L23/0815Copolymers of ethene with aliphatic 1-olefins
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L23/00Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
    • C08L23/02Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
    • C08L23/10Homopolymers or copolymers of propene
    • C08L23/14Copolymers of propene
    • C08L23/142Copolymers of propene at least partially crystalline copolymers of propene with other olefins
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C35/00Heating, cooling or curing, e.g. crosslinking or vulcanising; Apparatus therefor
    • B29C35/02Heating or curing, e.g. crosslinking or vulcanizing during moulding, e.g. in a mould
    • B29C35/08Heating or curing, e.g. crosslinking or vulcanizing during moulding, e.g. in a mould by wave energy or particle radiation
    • B29C35/0805Heating or curing, e.g. crosslinking or vulcanizing during moulding, e.g. in a mould by wave energy or particle radiation using electromagnetic radiation
    • B29C2035/0861Heating or curing, e.g. crosslinking or vulcanizing during moulding, e.g. in a mould by wave energy or particle radiation using electromagnetic radiation using radio frequency
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C65/00Joining or sealing of preformed parts, e.g. welding of plastics materials; Apparatus therefor
    • B29C65/02Joining or sealing of preformed parts, e.g. welding of plastics materials; Apparatus therefor by heating, with or without pressure
    • B29C65/04Dielectric heating, e.g. high-frequency welding, i.e. radio frequency welding of plastic materials having dielectric properties, e.g. PVC
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L101/00Compositions of unspecified macromolecular compounds
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L23/00Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
    • C08L23/02Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
    • C08L23/04Homopolymers or copolymers of ethene
    • C08L23/08Copolymers of ethene
    • C08L23/0846Copolymers of ethene with unsaturated hydrocarbons containing other atoms than carbon or hydrogen atoms
    • C08L23/0869Acids or derivatives thereof
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2314/00Polymer mixtures characterised by way of preparation
    • C08L2314/06Metallocene or single site catalysts
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L51/00Compositions of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L53/00Compositions of block copolymers containing at least one sequence of a polymer obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers
    • C08L53/02Compositions of block copolymers containing at least one sequence of a polymer obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers of vinyl-aromatic monomers and conjugated dienes
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L75/00Compositions of polyureas or polyurethanes; Compositions of derivatives of such polymers
    • C08L75/04Polyurethanes
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L77/00Compositions of polyamides obtained by reactions forming a carboxylic amide link in the main chain; Compositions of derivatives of such polymers
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/13Hollow or container type article [e.g., tube, vase, etc.]
    • Y10T428/1352Polymer or resin containing [i.e., natural or synthetic]
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/13Hollow or container type article [e.g., tube, vase, etc.]
    • Y10T428/1352Polymer or resin containing [i.e., natural or synthetic]
    • Y10T428/1386Natural or synthetic rubber or rubber-like compound containing
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/13Hollow or container type article [e.g., tube, vase, etc.]
    • Y10T428/1352Polymer or resin containing [i.e., natural or synthetic]
    • Y10T428/139Open-ended, self-supporting conduit, cylinder, or tube-type article
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/13Hollow or container type article [e.g., tube, vase, etc.]
    • Y10T428/1352Polymer or resin containing [i.e., natural or synthetic]
    • Y10T428/139Open-ended, self-supporting conduit, cylinder, or tube-type article
    • Y10T428/1393Multilayer [continuous layer]
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/31504Composite [nonstructural laminate]
    • Y10T428/31725Of polyamide
    • Y10T428/31739Nylon type
    • Y10T428/31743Next to addition polymer from unsaturated monomer[s]
    • Y10T428/31746Polymer of monoethylenically unsaturated hydrocarbon
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/31504Composite [nonstructural laminate]
    • Y10T428/31855Of addition polymer from unsaturated monomers
    • Y10T428/31909Next to second addition polymer from unsaturated monomers
    • Y10T428/31913Monoolefin polymer
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/31504Composite [nonstructural laminate]
    • Y10T428/31855Of addition polymer from unsaturated monomers
    • Y10T428/31909Next to second addition polymer from unsaturated monomers
    • Y10T428/31924Including polyene monomers
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/31504Composite [nonstructural laminate]
    • Y10T428/31855Of addition polymer from unsaturated monomers
    • Y10T428/31931Polyene monomer-containing

Definitions

  • the present invention relates generally to closures for flowable material containers and more particularly port tube assemblies for medical fluid containers.
  • the fluids to be administered to a patient are contained in a flexible container.
  • One method of forming a flexible container is to seal two sheets of flexible material about the periphery of the sheets to create a fluid tight chamber.
  • a port tube assembly is frequently placed between the sheets during the sealing process to create a communication between the fluid chamber and the exterior of the container to provide a means of introducing fluid into or dispensing fluid from the container.
  • the port tube assembly typically includes an outer port tube that attaches to the sidewalls of the container and a second tube called a membrane tube is disposed coaxially within the port tube.
  • the membrane tube has a membrane or diaphragm that seals the port tube assembly.
  • the membrane is typically punctured by a spike of a fluid administration set to place the contents of the container in fluid communication with a patient.
  • Port tubes and membrane tubes are fabricated from monolayer or multiple layered materials.
  • the port tube typically has an inner layer of polyvinyl chloride and the membrane tube has an outer layer of PVC.
  • the membrane tube is dipped in cyclohexanone or other suitable solvent and is inserted in a telescoping fashion into the port tube. The solvent melts the PVC of both the port tube and the membrane tube thereby hermetically sealing the membrane tube to the port tube.
  • Flexible PVC containers include low molecular weight additives know as plasticizers which may exude into the solutions contained in the container.
  • U.S. Pat. No. 5,356,709 discloses a non-PVC coextruded medical grade port tubing.
  • the tubing has an outer layer of a blend of polypropylene and SEBS a tie layer and a core layer of a blend of polyamide and EVA.
  • U.S. Pat. No. 5,533,992 assigned to the same assignee of the present invention, discloses a non-PVC material for fabricating medical tubings and medical containers.
  • Polymer blends for fabricating medical tubing disclosed in the '992 patent include polyurethane blended with one or more of the following: EVA, SEBS, PCCE, thermoplastic copolyester elastomers.
  • the present invention provides a non-PVC port tube, a non-PVC membrane tube and a non-PVC port tube assembly for use in flowable material containers such as medical and food containers.
  • the closure assembly includes a port tube and a membrane tube coaxially mounted therein.
  • the port tube has a first layer and a second layer.
  • the first layer is a multiple component polymer blend having a first component in an amount by weight of from about 25% to about 50% by weight of the first layer.
  • the first component is a first polyolefin selected from the group consisting of polypropylene and polypropylene copolymers.
  • the second component is present in an amount by weight of from about 0% to about 50% by weight of the first layer and is a second polyolefin.
  • the second polyolefin is selected from the group consisting of ethylene copolymers, ultra-low density polyethylene, polybutene, polybutadiene and butene ethylene copolymers.
  • the third component is present in an amount by weight of from about 0% to about 40% by weight of the first layer and is a radio frequency (“RF”) susceptible polymer.
  • the RF polymer is selected from the group consisting of polyamides, ethylene acrylic acid copolymers, ethylene methacrylic acid copolymers, polyimides, polyurethanes, polyesters, polyureas, ethylene vinyl acetate copolymers with a vinyl acetate comonomer content from 12%-50% by weight of the copolymer, ethylene methyl acrylate copolymers with methyl acrylate comonomer content from 12%-40% by weight of the copolymer, ethylene vinyl alcohol with vinyl alcohol comonomer content from 12%-70% by mole percent of the copolymer.
  • the fourth component is present in an amount from about 0% to about 40% and is a first thermoplastic elastomer.
  • the second layer of the port tube is disposed coaxially within the first layer and in a preferred form of the invention is a polymeric material that is susceptible of solvent bonding and more preferably includes a second thermoplastic elastomer.
  • the second layer can include an additive from about 0% to about 20% by weight of a polypropylene, high density polyethylene, silica, slip agents, fatty amides, acrawax and the like.
  • the membrane tube has an outer layer, a core layer and an inner layer.
  • the outer layer of the membrane tube is capable of being solvent bonded to the second layer of the port tube.
  • the outer layer of the membrane tube (A) is a polymer blend of: (1) from about 0% to about 60% by weight of the outer layer of a third polyolefin and (2) from about 40% to about 100% by weight of the outer layer of a second component of a third thermoplastic elastomer.
  • the core layer (B) is attached to the outer layer.
  • the core layer is a polymer blend of: (1) from about 35% to about 100% by weight of the core layer of a fourth thermoplastic elastomer and (2) from about 0% to about 65% by weight of the core layer of a fourth polyolefin.
  • the inner layer of the membrane tube is attached to the core layer on a side opposite of the outer layer.
  • the inner layer is a multiple component polymer blend of and in a preferred form has: (1) from about 25% to about 55% by weight of the inner layer a fifth polyolefin, (2) from about 0% to about 50% by weight of the inner layer a sixth polyolefin selected from the group consisting of ethylene copolymers, ultra-low density polyethylene, polybutene, and butene ethylene copolymers; (3) from about 0% to about 40% by weight of the inner layer of a radio frequency susceptible polymer selected from the group consisting of polyamides, ethylene acrylic acid copolymers, ethylene methacrylic acid copolymers, polyimides, polyurethanes, polyesters, polyureas, ethylene vinyl acetate copolymers with a vinyl acetate comonomer content from 12%-50% by weight of the copolymer, ethylene methyl acrylate copolymers with methyl acrylate
  • FIG. 1 is a plan view of a flowable material container with port closure assembly.
  • FIG. 2 is a cross-sectional view of a port tube of the present invention.
  • FIG. 1 shows a flowable material container 10 having sidewalls 12 sealed along peripheral edges to define a chamber 14 therebetween.
  • a port tube closure assembly 16 provides access to the contents of the container.
  • the container 10 is preferably fabricated from a non-PVC containing material.
  • the sidewalls 12 are fabricated from a multiple component polymer alloy such as those disclosed in detail in U.S. Pat. No. 5,686,527 which is incorporated herein by reference and made a part hereof.
  • One particularly suitable polymer alloy is a blend of polypropylene, ultra-low density polyethylene, a polyamide and a styrene and hydrocarbon block copolymer.
  • the container 10 shown in FIG. 1 is particularly suitable for medical applications such as storage and delivery of I.V.
  • peritoneal dialysis solutions peritoneal dialysis solutions
  • pharmaceutical drugs and blood and blood components to name a few. It is contemplated that such a container can also be used to store food products, serve as a drain bag for peritoneal dialysis or store other consumable products.
  • flowable material is a material that will flow by the force of gravity. Flowable materials therefore include both liquid items and powdered or granular items and the like.
  • FIG. 2 shows the port tube assembly 16 .
  • the port tube assembly 16 has a port tube 18 and a membrane tube 20 coaxially mounted therein.
  • a fluid passageway 22 of the membrane tube 20 is sealed by a membrane 23 positioned at an intermediate portion of the membrane tube 20 .
  • the membrane 23 can be punctured by a spike of an infusion set to place the contents of the container into fluid communication with, for example, the vascular system of a patient being treated.
  • the port tube 18 is a multilayered structure and more preferably has a first layer 22 and a second layer 24 .
  • the first layer 22 should be of a non-PVC containing material that is capable of being sealed to the sidewalls 12 of the container 10 , and preferably sealed using radio frequency sealing techniques.
  • the first layer 22 is a polymer blend of: (a) from about 25% to about 50%, more preferably from about 30% to about 40%, by weight of the first layer a first polyolefin selected from the group consisting of polypropylene and polypropylene copolymers, (b) from about 0% to about 50%, more preferably from about 5% to about 40%, by weight of the first layer a second polyolefin of an ⁇ -olefin containing polymer or copolymer and more preferably is an ethylene and ⁇ -olefin copolymer; (c) from about 0% to about 40%, more preferably from about 10% to about 40% of the first layer a radio frequency susceptible polymer selected from the group consisting of polyamides, ethylene acrylic acid copolymers, ethylene methacrylic acid copolymers, polyimides, polyurethanes, polyesters, polyureas, ethylene vinyl acetate copolymers with a vinyl acetate comonomer content from
  • the second layer 24 of the port tube 18 is of a non-PVC containing material that is capable of being solvent bonded to the membrane tube 20 .
  • the second layer 24 is a thermoplastic elastomer or a blend of a thermoplastic elastomer in an amount by weight of from about 80% to about 100% and a propylene containing polymer from about 0% to about 20% by weight of the second layer 24 . It is also desirable, but optional, that the second layer 24 softens slightly at autoclave temperatures so that when the port tube and membrane tube assembly is steam sterilized, the port tube more tightly adheres to the membrane tube.
  • the first layer has a thickness greater than the second layer.
  • the first layer will have a thickness of from about 15 mils to about 40 mils and more preferably from about 20 mils to about 30 mils.
  • the second layer will have a thickness from about 2 mils to about 10 mils and more preferably from about 3 mils to about 7 mils.
  • the membrane tube 20 should be fabricated from a non-PVC containing material and should be capable of being bonded to the port tube 18 , preferably using solvent bonding techniques.
  • Solvent bonding is well known in the art. Solvent bonding typically includes applying a solvent to a polymeric material to partially dissolve the polymer. While in this dissolved state the dissolved polymer material is placed in contact with a material, such as another polymer, that the polymeric material is to be bonded to.
  • Suitable solvents for solvent bonding of the materials of the present invention include at least the following aromatic solvents: cyclohexane, cyclohexanone, toluene, tetrahydofuran, cumene, xylenes, diethyl benzene, decalin, tetralin and amyl benzene to name a few.
  • a portion of the membrane tube that is to be in contact with the port tube is exposed to the solvent, typically by dipping the relevant portion of the membrane tube into the solvent. Then the membrane tube is inserted into the membrane tube in telescoping fashion where a strong bond is formed.
  • the membrane tube 20 is a multilayered structure having an outer layer 30 , a core layer 32 and an inner layer 34 .
  • the outer layer 30 is a polymer blend of: (a) from about 0% to about 60%, more preferably from about 20% to about 55% and most preferably from about 30% to about 50%, by weight of the outer layer of a polyolefin and (b) from about 40% to about 100%, more preferably from about 45% to about 80% and most preferably from about 50% to about 70%, by weight of the outer layer of a thermoplastic elastomer.
  • the core layer 32 is a polymer blend of: (a) from about 35% to about 100%, more preferably from about 50% to about 90% and most preferably 70% to about 90%, by weight of the core layer of a thermoplastic elastomer and (b) from about 0% to about 65%, more preferably from about 10% to about 50% and most preferably from about 10% to about 30%, by weight of the core layer of a polyolefin.
  • the inner layer 34 is a polymer blend of: (a) from about 25% to about 55%, more preferably from about 25% to about 40%, by weight of the inner layer a polyolefin; (b) from about 0% to about 50%, more preferably from about 0% to about 40% and most preferably 0% to about 20%, by weight of the inner layer a polyolefin selected from the group consisting of ⁇ -olefin containing polymers or copolymers and more preferably is an ethylene and ⁇ -olefin copolymer; (c) from about 0% to about 40% by weight, more preferably from about 15% to about 40%, of the inner layer a radio frequency susceptible polymer selected from the group consisting of polyamides, ethylene acrylic acid copolymers, ethylene methacrylic acid copolymers, polyimides, polyurethanes, polyesters, polyureas, ethylene vinyl acetate copolymers with a vinyl acetate comonomer content from
  • the outer layer 30 will have a thickness from about 3 mils to about 15 mils and more preferably from about 3 mils to about 10 mils.
  • the core layer 32 will have a thickness from about 10 mils to about 35 mils and more preferably from about 10 mils to about 30 mils.
  • the inner layer 34 will have a thickness from about 3 mils to about 15 mils and more preferably from about 5 mils to about 10 mils.
  • Thermoplastic elastomers include styrene and hydrocarbon copolymers, EPDM, and ethylene propylene rubber.
  • the styrene can be substituted or unsubstituted styrene.
  • the styrene and hydrocarbon copolymers can be block copolymer including di-block, tri-block, star block, it can also be a random copolymer and other types of styrene and hydrocarbon copolymers that are known by those skilled in the art.
  • Styrene and hydrocarbon copolymers therefore include for example, but are not limited to, styrene-butene-styrene block copolymer, styrene-ethylene-butene-styrene block copolymers, styrene-isobutene-styrene and the numerous other varieties of styrene and hydrocarbon copolymers that are well known in the art.
  • the styrene and hydrocarbon copolymers can also be blends of various types of the above-identified styrene and hydrocarbon copolymers.
  • thermoplastic elastomer of the first layer 22 of the port tube 18 and the inner layer 34 of the membrane tube 20 is an SEBS copolymer with a maleic anhydride group in an amount by weight of about 2% or less.
  • SEBS copolymer is sold by Shell Chemical Company under the tradename KRATON® FG1924X and FG1901X.
  • the thermoplastic elastomer of the second layer 24 of the port tube 18 and the outer layer 30 of the membrane tube 20 is preferably a styrene and diene copolymer more preferably selected from the group consisting of styrene-ethylene-butene-styrene copolymers, and styrene-isoprene-styrene copolymers. More preferably the thermoplastic elastomer of the second layer is an ethylene butene copolymer, and more preferably a styrene-ethylene-butene-styrene copolymer. It has been found that such a copolymer is well suited for solvent bonding. Suitable SEBS copolymers are sold by Shell Chemical Company under the tradename KRATON® KG1657.
  • thermoplastic elastomer of the core layer of the membrane tube is an SEBS copolymer containing a high proportion of triblock. Suitable polymers are sold by Shell Chemical Company under the tradename KRATON®KG1660, KG1652 and KG1650.
  • Suitable polypropylene polymers include homopolymers and copolymers.
  • Suitable comonomers are ⁇ -olefin s having from 2 to 17 carbons and most preferably is ethylene in an amount by weight from about 1 to about 8% by weight of the copolymer.
  • Suitable ⁇ -olefin containing polymers include homopolymers, copolymers and interpolymers of ⁇ -olefins having from 2 to 17 carbons.
  • Suitable ethylene ⁇ -olefin copolymers of the first layer 22 of the port tube 18 and the inner layer 34 of the membrane tube 20 have a density, as measured by ASTM D-792, of less than about 0.915 g/cc, more preferably less than about 0.905 g/cc, and are commonly referred to as very low density polylethylene (VLDPE), ultra low density polyethylene (ULDPE) and the like.
  • VLDPE very low density polylethylene
  • ULDPE ultra low density polyethylene
  • the ethylene and ⁇ -olefin copolymers are obtained using a single site catalyst such as metallocene catalysts, vanadium catalysts and the like.
  • a single site catalyst such as metallocene catalysts, vanadium catalysts and the like.
  • Suitable catalyst systems are those disclosed in U.S. Pat. Nos. 5,783,638 and 5,272,236.
  • Suitable ethylene and ⁇ -olefin copolymers include those sold by Dow Chemical Company under the AFFINITY tradename, Dupont-Dow under the ENGAGE tradename, Exxon under the EXACT tradename and Phillips Chemical Company under the tradename MARLEX.
  • the port tube assembly in a preferred form of the invention satisfies the following physical properties: (1) has a spike insertion force of less than about 35 lbs on average, (2) has a spike removal force of greater than about 5 lbs on average. The pull force to separate the membrane tube from the port tube is greater than the spike removal force.
  • a two layered port tube having an outer and an inner layer was coextruded.
  • the inner layer had a thickness of 0.006 inches and was fabricated from SEBS.
  • the outer layer had a thickness of 0.026 inches and was fabricated from a polymer blend by weight of the outer layer of 35% polypropylene/5% ultra low density polyethylene/30% dimer fatty acid polyamide/30% SEBS with maleic anhydride functionality.
  • a three layered membrane tube was coextruded having an inner layer, a core layer and an outer layer.
  • the inner layer is a polymer blend by weight 30% polypropylene/35% dimer fatty acid polyamide/35% SEBS.
  • the core layer was a blend of 85% SEBS and 15% polypropylene.
  • the outer layer was 45% SEBS and 55% polypropylene.
  • the inner layer had a thickness of 0.003 inches, the core layer 0.023 inches and the outer layer 0.006 inches.
  • Polymeric sheeting was extruded from a blend by weight of 10% dimer fatty acid polyamide, 35% ultra low density polyethylene, 45% polypropylene and 10% SEBS with maleic anhydride functionality.
  • a port tube segment was inserted into an open end of the pouch and was heat sealed therein while sealing the final peripheral edge to define a container.
  • a membrane tube segment was dipped into cyclohexanone and inserted in a telescoping fashion into the port tube segment.
  • the container was bolted down proximate a mechanical tester.
  • the port tube was attached to a spike attached to a cross-head of the mechanical tester.
  • the cross-head speed of the tester was set at 20 in/min.
  • the cross-head was set to achieve the desired spike insertion depth in the port tube.
  • the tester allowed for measuring the spike insertion force and the spike removal force.
  • the average spike insertion value after 50 tests was 13.31 lbf.
  • the average spike removal force for 50 tests was 10.37 lbf.
  • the tester was also used to determine the pull force necessary to remove the port tube from the container or to otherwise damage the container or port tube.
  • the port tube was inserted into the tester with the container bolted down.
  • the average pull force for 28 tests was 30.04 lbf. This test was conducted prior to steam sterilizing the container.
  • the value for 30 test after the container was steam sterilized was 42.68 lbf.

Abstract

The present invention provides a flowable material container closure assembly having a port tube and a membrane tube. The port tube (I) has a first layer and a second layer, (A) the first layer is a polymer blend of: (1) from about 25% to about 50% by weight of the first layer a first polyolefin selected from the group consisting of polypropylene and polypropylene copolymers, (2) from about 0 to about 50% by weight of the first layer a second polyolefin selected from the group consisting of ethylene copolymers, ultra-low density polyethylene, polybutene, and butene ethylene copolymers; (3) from about 0% to about 40% by weight of the first layer a radio frequency susceptible polymer selected from the group consisting of polyamides, ethylene acrylic acid copolymers, ethylene methacrylic acid copolymers, polyimides, polyurethanes, polyesters, polyureas, ethylene vinyl acetate copolymers with a vinyl acetate comonomer content from 12%-50% by weight of the copolymer, ethylene methyl acrylate copolymers with methyl acrylate comonomer content from 12%-40% by weight of the copolymer, ethylene vinyl alcohol with vinyl alcohol comonomer content from 12%-70% by mole percent of the copolymer; (4) from about 0% to about 40% of a first thermoplastic elastomer; and (B) the second layer is disposed coaxially within the first layer and is a second thermoplastic elastomer; and the (II) membrane tube is disposed coaxially within the port tube, the membrane tube has an outer layer, a core layer and an inner layer, the outer layer (A) is a polymer blend of: (1) from about 0% to about 60% by weight of the outer layer of a third polyolefin and (2) from about 40% to about 100% by weight of the outer layer of a second component of a third thermoplastic elastomer, the core layer (B) is attached to the outer layer, the core layer is a polymer blend of: (1) from about 35% to about 100% by weight of the core layer of a fourth thermoplastic elastomer and (2) from about 0% to about 65% by weight of the core layer of a fourth polyolefin; and (C) the inner layer is attached to the core layer on a side opposite of the outer layer, the inner layer is a polymer blend of: (1) from about 25% to about 55% by weight of the inner layer a fifth polyolefin, (2) from about 0 to about 50% by weight of the inner layer a sixth polyolefin selected from the group consisting of ethylene copolymers, ultra-low density polyethylene, polybutene, polybutadiene and butene ethylene copolymers; (3) from about 0% to about 60% by weight of the inner layer a radio frequency susceptible polymer selected from the group consisting of polyamides, ethylene acrylic acid copolymers, ethylene methacrylic acid copolymers, polyimides, polyurethanes, polyesters, polyureas, ethylene vinyl acetate copolymers with a vinyl acetate comonomer content from 12%-50% by weight of the copolymer, ethylene methyl acrylate copolymers with methyl acrylate comonomer content from 12%-40% by weight of the copolymer, ethylene vinyl alcohol with vinyl alcohol comonomer content from 12%-70% by mole percent of the copolymer; (4) from about 0% to about 40% by weight of the inner layer of a fifth thermoplastic elastomer.

Description

    TECHNICAL FIELD
  • The present invention relates generally to closures for flowable material containers and more particularly port tube assemblies for medical fluid containers.
  • BACKGROUND OF THE INVENTION
  • It is common medical practice to provide fluids to a patient either intravenously or enterally as a method of treating a patient for various medical conditions. Frequently, the fluids to be administered to a patient are contained in a flexible container. One method of forming a flexible container is to seal two sheets of flexible material about the periphery of the sheets to create a fluid tight chamber. A port tube assembly is frequently placed between the sheets during the sealing process to create a communication between the fluid chamber and the exterior of the container to provide a means of introducing fluid into or dispensing fluid from the container. The port tube assembly typically includes an outer port tube that attaches to the sidewalls of the container and a second tube called a membrane tube is disposed coaxially within the port tube. The membrane tube has a membrane or diaphragm that seals the port tube assembly. The membrane is typically punctured by a spike of a fluid administration set to place the contents of the container in fluid communication with a patient.
  • Port tubes and membrane tubes are fabricated from monolayer or multiple layered materials. The port tube typically has an inner layer of polyvinyl chloride and the membrane tube has an outer layer of PVC. To assemble the port tube assembly, the membrane tube is dipped in cyclohexanone or other suitable solvent and is inserted in a telescoping fashion into the port tube. The solvent melts the PVC of both the port tube and the membrane tube thereby hermetically sealing the membrane tube to the port tube.
  • There has been a great effort by many manufacturers of medical articles to replace PVC materials with non-PVC containing materials. Flexible PVC containers include low molecular weight additives know as plasticizers which may exude into the solutions contained in the container. U.S. Pat. Nos. 5,998,019 and 5,849,843, which are incorporated herein by reference and made a part hereof, disclose replacing PVC materials in medical fluid containers with non-PVC containing materials.
  • U.S. Pat. No. 5,356,709, assigned to the same assignee of the present invention, discloses a non-PVC coextruded medical grade port tubing. The tubing has an outer layer of a blend of polypropylene and SEBS a tie layer and a core layer of a blend of polyamide and EVA.
  • U.S. Pat. No. 5,533,992, assigned to the same assignee of the present invention, discloses a non-PVC material for fabricating medical tubings and medical containers. Polymer blends for fabricating medical tubing disclosed in the '992 patent include polyurethane blended with one or more of the following: EVA, SEBS, PCCE, thermoplastic copolyester elastomers.
  • SUMMARY OF THE INVENTION
  • The present invention provides a non-PVC port tube, a non-PVC membrane tube and a non-PVC port tube assembly for use in flowable material containers such as medical and food containers.
  • The closure assembly includes a port tube and a membrane tube coaxially mounted therein. The port tube has a first layer and a second layer. The first layer is a multiple component polymer blend having a first component in an amount by weight of from about 25% to about 50% by weight of the first layer. The first component is a first polyolefin selected from the group consisting of polypropylene and polypropylene copolymers. The second component is present in an amount by weight of from about 0% to about 50% by weight of the first layer and is a second polyolefin. The second polyolefin is selected from the group consisting of ethylene copolymers, ultra-low density polyethylene, polybutene, polybutadiene and butene ethylene copolymers. The third component is present in an amount by weight of from about 0% to about 40% by weight of the first layer and is a radio frequency (“RF”) susceptible polymer. The RF polymer is selected from the group consisting of polyamides, ethylene acrylic acid copolymers, ethylene methacrylic acid copolymers, polyimides, polyurethanes, polyesters, polyureas, ethylene vinyl acetate copolymers with a vinyl acetate comonomer content from 12%-50% by weight of the copolymer, ethylene methyl acrylate copolymers with methyl acrylate comonomer content from 12%-40% by weight of the copolymer, ethylene vinyl alcohol with vinyl alcohol comonomer content from 12%-70% by mole percent of the copolymer. The fourth component is present in an amount from about 0% to about 40% and is a first thermoplastic elastomer.
  • The second layer of the port tube is disposed coaxially within the first layer and in a preferred form of the invention is a polymeric material that is susceptible of solvent bonding and more preferably includes a second thermoplastic elastomer. Optionally, the second layer can include an additive from about 0% to about 20% by weight of a polypropylene, high density polyethylene, silica, slip agents, fatty amides, acrawax and the like.
  • The membrane tube has an outer layer, a core layer and an inner layer. The outer layer of the membrane tube is capable of being solvent bonded to the second layer of the port tube. In a preferred form of the invention, the outer layer of the membrane tube (A) is a polymer blend of: (1) from about 0% to about 60% by weight of the outer layer of a third polyolefin and (2) from about 40% to about 100% by weight of the outer layer of a second component of a third thermoplastic elastomer. The core layer (B) is attached to the outer layer. In a preferred form of the invention, the core layer is a polymer blend of: (1) from about 35% to about 100% by weight of the core layer of a fourth thermoplastic elastomer and (2) from about 0% to about 65% by weight of the core layer of a fourth polyolefin.
  • The inner layer of the membrane tube is attached to the core layer on a side opposite of the outer layer. The inner layer is a multiple component polymer blend of and in a preferred form has: (1) from about 25% to about 55% by weight of the inner layer a fifth polyolefin, (2) from about 0% to about 50% by weight of the inner layer a sixth polyolefin selected from the group consisting of ethylene copolymers, ultra-low density polyethylene, polybutene, and butene ethylene copolymers; (3) from about 0% to about 40% by weight of the inner layer of a radio frequency susceptible polymer selected from the group consisting of polyamides, ethylene acrylic acid copolymers, ethylene methacrylic acid copolymers, polyimides, polyurethanes, polyesters, polyureas, ethylene vinyl acetate copolymers with a vinyl acetate comonomer content from 12%-50% by weight of the copolymer, ethylene methyl acrylate copolymers with methyl acrylate comonomer content from 12%-40% by weight of the copolymer, ethylene vinyl alcohol with vinyl alcohol comonomer content from 12%-70% by mole percent of the copolymer; and (4) from about 0% to about 40% by weight of the inner layer of a fifth thermoplastic elastomer.
  • BRIEF DESCRIPTION OF THE DRAWINGS
  • FIG. 1 is a plan view of a flowable material container with port closure assembly.
  • FIG. 2 is a cross-sectional view of a port tube of the present invention.
  • DETAILED DESCRIPTION
  • The present invention is susceptible of embodiments in many different forms. Preferred embodiments of the invention are disclosed with the understanding that the present disclosure is to be considered as exemplifications of the principles of the invention and are not intended to limit the broad aspects of the invention to the embodiments illustrated.
  • FIG. 1 shows a flowable material container 10 having sidewalls 12 sealed along peripheral edges to define a chamber 14 therebetween. A port tube closure assembly 16 provides access to the contents of the container. The container 10 is preferably fabricated from a non-PVC containing material. In a preferred form of the invention the sidewalls 12 are fabricated from a multiple component polymer alloy such as those disclosed in detail in U.S. Pat. No. 5,686,527 which is incorporated herein by reference and made a part hereof. One particularly suitable polymer alloy is a blend of polypropylene, ultra-low density polyethylene, a polyamide and a styrene and hydrocarbon block copolymer. The container 10 shown in FIG. 1 is particularly suitable for medical applications such as storage and delivery of I.V. solutions, peritoneal dialysis solutions, pharmaceutical drugs and blood and blood components to name a few. It is contemplated that such a container can also be used to store food products, serve as a drain bag for peritoneal dialysis or store other consumable products.
  • What is meant by “flowable material” is a material that will flow by the force of gravity. Flowable materials therefore include both liquid items and powdered or granular items and the like.
  • FIG. 2 shows the port tube assembly 16. The port tube assembly 16 has a port tube 18 and a membrane tube 20 coaxially mounted therein. A fluid passageway 22 of the membrane tube 20 is sealed by a membrane 23 positioned at an intermediate portion of the membrane tube 20. For medical applications, the membrane 23 can be punctured by a spike of an infusion set to place the contents of the container into fluid communication with, for example, the vascular system of a patient being treated.
  • In a preferred form of the invention the port tube 18 is a multilayered structure and more preferably has a first layer 22 and a second layer 24. The first layer 22 should be of a non-PVC containing material that is capable of being sealed to the sidewalls 12 of the container 10, and preferably sealed using radio frequency sealing techniques. In a preferred form of the invention the first layer 22 is a polymer blend of: (a) from about 25% to about 50%, more preferably from about 30% to about 40%, by weight of the first layer a first polyolefin selected from the group consisting of polypropylene and polypropylene copolymers, (b) from about 0% to about 50%, more preferably from about 5% to about 40%, by weight of the first layer a second polyolefin of an α-olefin containing polymer or copolymer and more preferably is an ethylene and α-olefin copolymer; (c) from about 0% to about 40%, more preferably from about 10% to about 40% of the first layer a radio frequency susceptible polymer selected from the group consisting of polyamides, ethylene acrylic acid copolymers, ethylene methacrylic acid copolymers, polyimides, polyurethanes, polyesters, polyureas, ethylene vinyl acetate copolymers with a vinyl acetate comonomer content from 12%-50% by weight of the copolymer, ethylene methyl acrylate copolymers with methyl acrylate comonomer content from 12%-40% by weight of the copolymer, ethylene vinyl alcohol with vinyl alcohol comonomer content from 12%-70% by mole percent of the copolymer; and (d) from about 0% to about 40%, more preferably from about 10% to about 40% of a thermoplastic elastomer by weight of the first layer.
  • The second layer 24 of the port tube 18 is of a non-PVC containing material that is capable of being solvent bonded to the membrane tube 20. In a preferred form of the invention the second layer 24 is a thermoplastic elastomer or a blend of a thermoplastic elastomer in an amount by weight of from about 80% to about 100% and a propylene containing polymer from about 0% to about 20% by weight of the second layer 24. It is also desirable, but optional, that the second layer 24 softens slightly at autoclave temperatures so that when the port tube and membrane tube assembly is steam sterilized, the port tube more tightly adheres to the membrane tube.
  • As shown in the Figures, the first layer has a thickness greater than the second layer. In a preferred form of the invention the first layer will have a thickness of from about 15 mils to about 40 mils and more preferably from about 20 mils to about 30 mils. The second layer will have a thickness from about 2 mils to about 10 mils and more preferably from about 3 mils to about 7 mils.
  • The membrane tube 20 should be fabricated from a non-PVC containing material and should be capable of being bonded to the port tube 18, preferably using solvent bonding techniques. Solvent bonding is well known in the art. Solvent bonding typically includes applying a solvent to a polymeric material to partially dissolve the polymer. While in this dissolved state the dissolved polymer material is placed in contact with a material, such as another polymer, that the polymeric material is to be bonded to. Suitable solvents for solvent bonding of the materials of the present invention include at least the following aromatic solvents: cyclohexane, cyclohexanone, toluene, tetrahydofuran, cumene, xylenes, diethyl benzene, decalin, tetralin and amyl benzene to name a few.
  • Accordingly, to solvent bond the membrane tube to the port tube, a portion of the membrane tube that is to be in contact with the port tube is exposed to the solvent, typically by dipping the relevant portion of the membrane tube into the solvent. Then the membrane tube is inserted into the membrane tube in telescoping fashion where a strong bond is formed.
  • In a preferred form of the invention the membrane tube 20 is a multilayered structure having an outer layer 30, a core layer 32 and an inner layer 34. In a preferred form of the invention the outer layer 30 is a polymer blend of: (a) from about 0% to about 60%, more preferably from about 20% to about 55% and most preferably from about 30% to about 50%, by weight of the outer layer of a polyolefin and (b) from about 40% to about 100%, more preferably from about 45% to about 80% and most preferably from about 50% to about 70%, by weight of the outer layer of a thermoplastic elastomer.
  • Also, in a preferred form of the invention the core layer 32 is a polymer blend of: (a) from about 35% to about 100%, more preferably from about 50% to about 90% and most preferably 70% to about 90%, by weight of the core layer of a thermoplastic elastomer and (b) from about 0% to about 65%, more preferably from about 10% to about 50% and most preferably from about 10% to about 30%, by weight of the core layer of a polyolefin.
  • Also, in a preferred form of the invention, the inner layer 34 is a polymer blend of: (a) from about 25% to about 55%, more preferably from about 25% to about 40%, by weight of the inner layer a polyolefin; (b) from about 0% to about 50%, more preferably from about 0% to about 40% and most preferably 0% to about 20%, by weight of the inner layer a polyolefin selected from the group consisting of α-olefin containing polymers or copolymers and more preferably is an ethylene and α-olefin copolymer; (c) from about 0% to about 40% by weight, more preferably from about 15% to about 40%, of the inner layer a radio frequency susceptible polymer selected from the group consisting of polyamides, ethylene acrylic acid copolymers, ethylene methacrylic acid copolymers, polyimides, polyurethanes, polyesters, polyureas, ethylene vinyl acetate copolymers with a vinyl acetate comonomer content from 12%-50% by weight of the copolymer, ethylene methyl acrylate copolymers with methyl acrylate comonomer content from 12%-40% by weight of the copolymer, ethylene vinyl alcohol with vinyl alcohol comonomer content from 12%-70% by mole percent of the copolymer; and (d) from about 0% to about 40%, more preferably from about 15% to about 40%, by weight of the inner layer of a thermoplastic elastomer.
  • In a preferred form of the invention the outer layer 30 will have a thickness from about 3 mils to about 15 mils and more preferably from about 3 mils to about 10 mils. The core layer 32 will have a thickness from about 10 mils to about 35 mils and more preferably from about 10 mils to about 30 mils. The inner layer 34 will have a thickness from about 3 mils to about 15 mils and more preferably from about 5 mils to about 10 mils.
  • Thermoplastic elastomers include styrene and hydrocarbon copolymers, EPDM, and ethylene propylene rubber. The styrene can be substituted or unsubstituted styrene. The styrene and hydrocarbon copolymers can be block copolymer including di-block, tri-block, star block, it can also be a random copolymer and other types of styrene and hydrocarbon copolymers that are known by those skilled in the art. Styrene and hydrocarbon copolymers therefore include for example, but are not limited to, styrene-butene-styrene block copolymer, styrene-ethylene-butene-styrene block copolymers, styrene-isobutene-styrene and the numerous other varieties of styrene and hydrocarbon copolymers that are well known in the art. The styrene and hydrocarbon copolymers can also be blends of various types of the above-identified styrene and hydrocarbon copolymers.
  • The styrene and hydrocarbon copolymers can be modified or functionalized by carboxylic acid groups, anhydrides of carboxylic acids, esters of carboxylic acids, epoxy groups and carbon monoxide. In a preferred form of the invention the thermoplastic elastomer of the first layer 22 of the port tube 18 and the inner layer 34 of the membrane tube 20 is an SEBS copolymer with a maleic anhydride group in an amount by weight of about 2% or less. Such a copolymer is sold by Shell Chemical Company under the tradename KRATON® FG1924X and FG1901X.
  • The thermoplastic elastomer of the second layer 24 of the port tube 18 and the outer layer 30 of the membrane tube 20 is preferably a styrene and diene copolymer more preferably selected from the group consisting of styrene-ethylene-butene-styrene copolymers, and styrene-isoprene-styrene copolymers. More preferably the thermoplastic elastomer of the second layer is an ethylene butene copolymer, and more preferably a styrene-ethylene-butene-styrene copolymer. It has been found that such a copolymer is well suited for solvent bonding. Suitable SEBS copolymers are sold by Shell Chemical Company under the tradename KRATON® KG1657.
  • The thermoplastic elastomer of the core layer of the membrane tube is an SEBS copolymer containing a high proportion of triblock. Suitable polymers are sold by Shell Chemical Company under the tradename KRATON®KG1660, KG1652 and KG1650.
  • Suitable polypropylene polymers include homopolymers and copolymers. Suitable comonomers are α-olefin s having from 2 to 17 carbons and most preferably is ethylene in an amount by weight from about 1 to about 8% by weight of the copolymer.
  • Suitable α-olefin containing polymers include homopolymers, copolymers and interpolymers of α-olefins having from 2 to 17 carbons. Suitable ethylene α-olefin copolymers of the first layer 22 of the port tube 18 and the inner layer 34 of the membrane tube 20 have a density, as measured by ASTM D-792, of less than about 0.915 g/cc, more preferably less than about 0.905 g/cc, and are commonly referred to as very low density polylethylene (VLDPE), ultra low density polyethylene (ULDPE) and the like. In a preferred form of the invention, the ethylene and α-olefin copolymers are obtained using a single site catalyst such as metallocene catalysts, vanadium catalysts and the like. Suitable catalyst systems, among others, are those disclosed in U.S. Pat. Nos. 5,783,638 and 5,272,236. Suitable ethylene and α-olefin copolymers include those sold by Dow Chemical Company under the AFFINITY tradename, Dupont-Dow under the ENGAGE tradename, Exxon under the EXACT tradename and Phillips Chemical Company under the tradename MARLEX.
  • The port tube assembly, in a preferred form of the invention satisfies the following physical properties: (1) has a spike insertion force of less than about 35 lbs on average, (2) has a spike removal force of greater than about 5 lbs on average. The pull force to separate the membrane tube from the port tube is greater than the spike removal force.
  • The following is a non-limiting example of the present invention.
  • EXAMPLES
  • A two layered port tube having an outer and an inner layer was coextruded. The inner layer had a thickness of 0.006 inches and was fabricated from SEBS. The outer layer had a thickness of 0.026 inches and was fabricated from a polymer blend by weight of the outer layer of 35% polypropylene/5% ultra low density polyethylene/30% dimer fatty acid polyamide/30% SEBS with maleic anhydride functionality.
  • A three layered membrane tube was coextruded having an inner layer, a core layer and an outer layer. The inner layer is a polymer blend by weight 30% polypropylene/35% dimer fatty acid polyamide/35% SEBS. The core layer was a blend of 85% SEBS and 15% polypropylene. The outer layer was 45% SEBS and 55% polypropylene. The inner layer had a thickness of 0.003 inches, the core layer 0.023 inches and the outer layer 0.006 inches.
  • Polymeric sheeting was extruded from a blend by weight of 10% dimer fatty acid polyamide, 35% ultra low density polyethylene, 45% polypropylene and 10% SEBS with maleic anhydride functionality.
  • Two rectangularly-shaped sheets of the polymeric sheeting were placed into registration and sealed along 3 peripheral edges to define a pouch. A port tube segment was inserted into an open end of the pouch and was heat sealed therein while sealing the final peripheral edge to define a container. A membrane tube segment was dipped into cyclohexanone and inserted in a telescoping fashion into the port tube segment.
  • The container was bolted down proximate a mechanical tester. The port tube was attached to a spike attached to a cross-head of the mechanical tester. The cross-head speed of the tester was set at 20 in/min. The cross-head was set to achieve the desired spike insertion depth in the port tube. The tester allowed for measuring the spike insertion force and the spike removal force. The average spike insertion value after 50 tests was 13.31 lbf. The average spike removal force for 50 tests was 10.37 lbf. These measurements were made after the spike dwelled in the membrane tube for 24 hours.
  • The tester was also used to determine the pull force necessary to remove the port tube from the container or to otherwise damage the container or port tube. The port tube was inserted into the tester with the container bolted down. The average pull force for 28 tests was 30.04 lbf. This test was conducted prior to steam sterilizing the container. The value for 30 test after the container was steam sterilized was 42.68 lbf.

Claims (72)

1-40. (canceled)
41. A flowable material container closure assembly comprising:
(I) a port tube having a first layer and a second layer, (A) the first layer is a polymer blend of: (1) from about 25% to about 50% by weight of the first layer a first polyolefin selected from the group consisting of polypropylene and polypropylene copolymers, (2) from about 0 to about 50% by weight of the first layer a second polyolefin selected from the group consisting of ethylene copolymers, ultra-low density polyethylene, polybutene, polybutadiene and butene ethylene copolymers; (3) from about 0% to about 40% by weight of the first layer a radio frequency susceptible polymer selected from the group consisting of polyamides, ethylene acrylic acid copolymers, ethylene methacrylic acid copolymers, polyimides, polyurethanes, polyesters, polyureas, ethylene vinyl acetate copolymers with a vinyl acetate comonomer content from 12%-50% by weight of the copolymer, ethylene methyl acrylate copolymers with methyl acrylate comonomer content from 12%-40% by weight of the copolymer, ethylene vinyl alcohol with vinyl alcohol comonomer content from 12%-70% by mole percent of the copolymer; (4) from about 0% to about 40% of a first thermoplastic elastomer; and (B) the second layer is disposed coaxially within the first layer and is a second thermoplastic elastomer; and
(II) a membrane tube disposed coaxially within the port tube.
42. The assembly of claim 41 wherein the membrane tube has multiple layers.
43. The assembly of claim 42 wherein the membrane tube has an outer layer, an inner layer, the outer layer is capable of solvent bonding.
44. The assembly of claim 43 wherein the membrane tube further comprises a core layer positioned between the outer layer and the inner layer.
45. The assembly of claim 43 wherein the outer layer (A) is a polymer blend of: (1) from about 0% to about 60% by weight of the outer layer of a third polyolefin and (2) from about 40% to about 100% by weight of the outer layer of a third thermoplastic elastomer, the core layer (B) is attached to the outer layer, the core layer is a polymer blend of: (1) from about 35% to about 100% by weight of the core layer of a fourth thermoplastic elastomer and (2) from about 0% to about 65% by weight of the core layer of a fourth polyolefin; and (C) the inner layer is attached to the core layer on a side opposite of the outer layer, the inner layer is a polymer blend of: (1) from about 25% to about 55% by weight of the inner layer a fifth polyolefin, (2) from about 0 to about 50% by weight of the inner layer a sixth polyolefin selected from the group consisting of ethylene copolymers, ultra-low density polyethylene, polybutene, polybutadiene and butene ethylene copolymers; (3) from about 0% to about 40% by weight of the inner layer a radio frequency susceptible polymer selected from the group consisting of polyamides, ethylene acrylic acid copolymers, ethylene methacrylic acid copolymers, polyimides, polyurethanes, polyesters, polyureas, ethylene vinyl acetate copolymers with a vinyl acetate comonomer content from 12%-50% by weight of the copolymer, ethylene methyl acrylate copolymers with methyl acrylate comonomer content from 12%-40% by weight of the copolymer, ethylene vinyl alcohol with vinyl alcohol comonomer content from 12%-70% by mole percent of the copolymer; and (4) from about 0% to about 40% by weight of the inner layer of a fifth thermoplastic elastomer.
46. The assembly of claim 41 wherein the polyamide is selected from a group consisting of: aliphatic polyamides re-sulting from the condensation reaction of di-amines having a carbon number within a range of 2-13, aliphatic polyamides resulting from a condensation reaction of di-acids having a carbon number within a range of 2-13, polyamides resulting from the condensation reaction of dimer fatty acids, and amide containing copolymers.
47. The assembly of claim 41 wherein the polyamide is a dimer fatty acid polyamide.
48. The assembly of claim 41 wherein the first polyolefin is a propylene copolymerized with a monomer selected from the group consisting of α-olefin s having from 2-17 carbons.
49. The assembly of claim 48 wherein the first polyolefin is a propylene and ethylene copolymer having an ethylene content of from about 1% to about 8% by weight of the first polyolefin.
50. The assembly of claim 41 wherein the second polyolefin is an ethylene copolymerized with a monomer selected from the group consisting of α-olefin s.
51. The assembly of claim 50 wherein the second polyolefin is an ethylene and α-olefin copolymer wherein the α-olefin has from 4 to 8 carbons.
52. The assembly of claim 51 wherein the ethylene and α-olefin copolymer is obtained using a single-site catalyst.
53. The assembly of claim 41 wherein the first thermoplastic elastomer is selected from the group consisting of a first styrene and hydrocarbon copolymer.
54. The assembly of claim 53 wherein the first styrene and hydrocarbon copolymer is selected from the group of styrene and hydrocarbon diblock copolymers, styrene and hydrocarbon triblock copolymers, styrene and hydrocarbon star block copolymers and blends of the same.
55. The assembly of claim 54 wherein the first thermoplastic elastomer is a first styrene-ethylene-butene-styrene block copolymer.
56. The assembly of claim 41 wherein the first thermoplastic elastomer is functionalized with a group selected from the group consisting of carboxylic acid, esters of carboxylic acids, anhydrides of carboxylic acids, epoxides, and carbon monoxide.
57. The assembly of claim 56 wherein the first thermoplastic elastomer is maleic anhydride functionalized.
58. The assembly of claim 41 wherein the second thermoplastic elastomer is selected from the group consisting of a second styrene and hydrocarbon copolymer.
59. The assembly of claim 58 wherein the second styrene and hydrocarbon copolymer is selected from the group if polymer structures with diblock copolymers, triblock, star block copolymers, and blends of the same.
60. The assembly of claim 59 wherein the second thermoplastic elastomer is a second styrene-ethylene-butene-styrene block copolymer.
61. The assembly of claim 60 wherein the second thermoplastic elastomer is a blend of a styrene-ethylene-butene-styrene diblock copolymer and a a styrene-ethylene-butene-styrene triblock copolymer.
62. A flowable material container closure assembly comprising:
(I) a port tube:
(II) a membrane tube disposed coaxially within the port tube, the membrane tube has an outer layer, a core layer and an inner layer, (A) the outer layer is a polymer blend of: (1) from about 0% to about 60% by weight of the outer layer of a first polyolefin and (2) from about 40% to about 100% by weight of the outer layer of a first thermoplastic elastomer, (B) the core layer is attached to the outer layer, the core layer is a polymer blend of: (1) from about 35% to about 100% by weight of the core layer of a second thermoplastic elastomer and (2) from about 0% to about 65% by weight of the core layer of a second polyolefin; and (C) the inner layer is attached to the core layer on a side opposite of the outer layer, the inner layer is a polymer blend of: (1) from about 25% to about 55% by weight of the inner layer a third polyolefin, (2) from about 0 to about 50% by weight of the inner layer a fourth polyolefin selected from the group consisting of ethylene copolymers, ultra-low density polyethylene, polybutene, and butene ethylene copolymers; (3) from about 0% to about 40% by weight of the inner layer a radio frequency susceptible polymer selected from the group consisting of polyamides, ethylene acrylic acid copolymers, ethylene methacrylic acid copolymers, polyimides, polyurethanes, polyesters, polyureas, ethylene vinyl acetate copolymers with a vinyl acetate comonomer content from 12%-50% by weight of the copolymer, ethylene methyl acrylate copolymers with methyl acrylate comonomer content from 12%-40% by weight of the copolymer, ethylene vinyl alcohol with vinyl alcohol comonomer content from 12%-70% by mole percent of the copolymer; and (4) from about 0% to about 40% by weight of the inner layer of a third thermoplastic elastomer.
63. The assembly of claim 62 wherein the port tube has a first layer and a second layer coaxially disposed within the first layer, the second layer is capable of solvent bonding to the outer layer of the membrane tube.
64. The assembly of claim 63 wherein (A) the first layer is a polymer blend of: (1) from about 25% to about 50% by weight of the first layer a fifth polyolefin selected from the group consisting of polypropylene and polypropylene copolymers, (2) from about 0 to about 50% by weight of the first layer a sixth polyolefin selected from the group consisting of ethylene copolymers, ultra-low density polyethylene, polybutene, polybutadiene and butene ethylene copolymers; (3) from about 0% to about 40% by weight of the first layer a radio frequency susceptible polymer selected from the group consisting of polyamides, ethylene acrylic acid copolymers, ethylene methacrylic acid copolymers, polyimides, polyurethanes, polyesters, polyureas, ethylene vinyl acetate copolymers with a vinyl acetate comonomer content from 12%-50% by weight of the copolymer, ethylene methyl acrylate copolymers with methyl acrylate comonomer content from 12%-40% by weight of the copolymer, ethylene vinyl alcohol with vinyl alcohol comonomer content from 12%-70% by mole percent of the copolymer; (4) from about 0% to about 40% of a fourth thermoplastic elastomer; and (B) the second layer is a fifth thermoplastic elastomer.
65. The assembly of claim 62 wherein the first polyolefin is selected from the group consisting of a polypropylene homopolymer, a propylene copolymerized with a monomer selected from the group consisting of α-olefin s having from 2-17 carbons, ethylene homopolymers and ethylene copolymerized with a monomer selected from the group consisting of α-olefin s having from 2-17 carbons.
66. The assembly of claim 65 wherein the first polyolefin is a propylene and ethylene copolymer having an ethylene content of from about 1% to about 8% by weight of the first polyolefin.
67. The assembly of claim 62 wherein the second polyolefin is selected from the group consisting of a polypropylene homopolymer, a propylene copolymerized with a monomer selected from the group consisting of α-olefin s having from 2-17 carbons, ethylene homopolymers and ethylene copolymerized with a monomer selected from the group consisting of α-olefin s having from 2-17 carbons.
68. The assembly of claim 62 wherein the third polyolefin is selected from the group consisting of a polypropylene homopolymer, a propylene copolymerized with a monomer selected from the group consisting of α-olefin s having from 2-17 carbons, ethylene homopolymers and ethylene copolymerized with a monomer selected from the group consisting of α-olefin s having from 2-17 carbons.
69. The assembly of claim 62 wherein the fourth polyolefin is an ethylene copolymerized with a monomer selected from the group consisting of α-olefin s.
70. The assembly of claim 69 wherein the ethylene and α-olefin copolymer is obtained using a single-site catalyst.
71. The assembly of claim 62 wherein the first thermoplastic elastomer is selected from the group consisting of a first styrene and hydrocarbon copolymers.
72. The assembly of claim 71 wherein the first styrene and hydrocarbon copolymer is selected from the group consisting of polymer structures of diblock, triblock, star block and blends of the same.
73. The assembly of claim 72 wherein the first thermoplastic elastomer is a first styrene-ethylene-butene-styrene block copolymer.
74. The assembly of claim 73 wherein the first thermoplastic elastomer is a blend of a styrene-ethylene-butene-styrene diblock copolymer and a a styrene-ethylene-butenestyrene triblock copolymer.
75. The assembly of claim 62 wherein the second thermoplastic elastomer is selected from the group consisting of a second styrene and hydrocarbon copolymer.
76. The assembly of claim 14 wherein the second styrene and hydrocarbon copolymer is selected from the group of polymer structures consisting of diblock, triblock and star block copolymers.
77. The assembly of claim 76 wherein the second thermoplastic elastomer is a second styrene-ethylene-butene-styrene block copolymer.
78. The assembly of claim 62 wherein the third thermoplastic elastomer is selected from the group consisting of a third styrene and hydrocarbon copolymer.
79. The assembly of claim 78 wherein the third styrene and hydrocarbon copolymer is selected from the group of polymer structures consisting of diblock, triblock and star block.
80. The assembly of claim 79 wherein the third thermoplastic elastomer is a third styrene-ethylene-butene-styrene block copolymer.
81. The assembly of claim 62 wherein the third thermoplastic elastomer is functionalized with a group selected from the group consisting of carboxlic acid, esters of carboxylic acids, anhydrides of carboxylic acids, epoxides, and carbon monoxide.
82. The assembly of claim 81 wherein the third thermoplastic elastomer is maleic anhydride functionalized.
83. A flowable material container closure assembly comprising:
(I) a port tube having a first layer and a second layer, (A) the first layer is a polymer blend of: (1) from about 25% to about 50% by weight of the first layer a first polyolefin selected from the group consisting of polypropylene and polypropylene copolymers, (2) from about 0% to about 50% by weight of the first layer a second polyolefin selected from the group consisting of ethylene copolymers, ultra-low density polyethylene, polybutene, and butene ethylene copolymers; (3) from about 0% to about 40% by weight of the first layer a radio frequency susceptible polymer selected from the group consisting of polyamides, ethylene acrylic acid copolymers, ethylene methacrylic acid copolymers, polyimides, polyurethanes, polyesters, polyureas, ethylene vinyl acetate copolymers with a vinyl acetate comonomer content from 12%-50% by weight of the copolymer, ethylene methyl acrylate copolymers with methyl acrylate comonomer content from 12%-40% by weight of the copolymer, ethylene vinyl alcohol with vinyl alcohol comonomer content from 12%-70% by mole percent of the copolymer; (4) from about 0% to about 40% of a first thermoplastic elastomer; and (B) the second layer is disposed coaxially within the first layer and is a second thermoplastic elastomer; and
(II) a membrane tube disposed coaxially within the port tube, the membrane tube has an outer layer, a core layer and an inner layer, the outer layer (A) is a polymer blend of: (1) from about 0% to about 60% by weight of the outer layer of a third polyolefin and (2) from about 40% to about 100% by weight of the outer layer of a second component of a third thermoplastic elastomer, the core layer (B) is attached to the outer layer, the core layer is a polymer blend of: (1) from about 35% to about 100% by weight of the core layer of a fourth thermoplastic elastomer and (2) from about 0% to about 65% by weight of the core layer of a fourth polyolefin; and (C) the inner layer is attached to the core layer on a side opposite of the outer layer, the inner layer is a polymer blend of: (1) from about 25% to about 55% Uy weight of the inner layer a fifth polyolefin, (2) from about 0% to about 50% by weight of the inner layer a sixth polyolefin selected from the group consisting of ethylene copolymers, ultra-low density polyethylene, polybutene, polybutadiene and butene ethylene copolymers; (3) from about 0% to about 40% by weight of the inner layer a radio frequency susceptible polymer selected from the group consisting of polyamides, ethylene acrylic acid copolymers, ethylene methacrylic acid copolymers, polyimides, polyurethanes, polyesters, polyureas, ethylene vinyl acetate copolymers with a vinyl acetate comonomer content from 12%-50% by weight of the copolymer, ethylene methyl acrylate copolymers with methyl acrylate comonomer content from 12%-40% by weight of the copolymer, ethylene vinyl alcohol with vinyl alcohol comonomer content from 12%-70% by mole percent of the copolymer; (4) from about 0% to about 40% by weight of the inner layer of a fifth thermoplastic elastomer.
84. The assembly of claim 83 wherein the polyamide is selected from a group consisting of: aliphatic polyamides re-sulting from the condensation reaction of di-amines having a carbon number within a range of 2-13, aliphatic polyamides resulting from a condensation reaction of di-acids having a carbon number within a range of 2-13, polyamides resulting from the condensation reaction of dimer fatty acids, and amide containing copolymers.
85. The assembly of claim 84 wherein the polyamide is a dimer fatty acid polyamide.
86. The assembly of claim 83 wherein the first polyolefin is a propylene copolymerized with a monomer selected from the group consisting of α-olefins having from 2-17 carbons.
87. The assembly of claim 86 wherein the first polyolefin is a propylene and ethylene copolymer having an ethylene content of from about 1% to about 8% by weight of the first polyolefin.
88. The assembly of claim 5 wherein the second polyolefin is an ethylene copolymerized with a monomer selected from the group consisting of α-olefins.
89. The assembly of claim 88 wherein the second polyolefin is an ethylene and α-olefin copolymer.
90. The assembly of claim 89 wherein the ethylene and α-olefin copolymer is obtained using a single-site catalyst.
91. The assembly of claim 89 wherein the first thermoplastic elastomer is selected from the group consisting of a first styrene and hydrocarbon copolymer.
92. The assembly of claim 91 wherein the first styrene and hydrocarbon copolymer is selected from the group of polymer structures consisting of diblock, triblock, and star block.
93. The assembly of claim 92 wherein the first thermoplastic elastomer is a first styrene-ethylene-butene-styrene block copolymer.
94. The assembly of claim 92 wherein the first thermoplastic elastomer is functionalized with a group selected from the group consisting of carboxlic acid, esters of carboxylic acids, anhydrides of carboxylic acids, epoxides, and carbon monoxide.
95. The assembly of claim 94 wherein the first thermoplastic elastomer is maleic anhydride functionalized.
96. The assembly of claim 92 wherein the second thermoplastic elastomer is selected from the group consisting of a second styrene and hydrocarbon copolymer.
97. The assembly of claim 96 wherein the second styrene and hydrocarbon copolymer is selected from the group of polymer structures consisting of diblock, triblock, and star block.
98. The assembly of claim 97 wherein the second thermoplastic elastomer is a second styrene-ethylene-butene-styrene block copolymer.
99. The assembly of claim 98 wherein the second thermoplastic elastomer is a styrene-ethylene-butene-styrene diblock copolymer and a styrene-ethylene-butene-styrene triblock copolymer.
100. The assembly of claim 97 wherein the third thermoplastic elastomer is a second styrene and hydrocarbon copolymer.
101. The assembly of claim 100 wherein the third thermoplastic elastomer is selected from the group of polymer structures consisting of diblock, triblock, and star block.
102. The assembly of claim 101 wherein the third thermoplastic elastomer is a blend of a styrene-ethylene-butene-styrene diblock copolymer and a a styrene-ethylene-butene-styrene triblock copolymer.
103. The assembly of claim 101 wherein the fourth thermoplastic elastomer is selected from the group consisting of a fourth styrene and hydrocarbon copolymers.
104. The assembly of claim 103 wherein the fourth styrene and hydrocarbon copolymer is selected from the group of polymer structures consisting of diblock, triblock, and star block copolymers.
105. The assembly of claim 104 wherein the fourth thermoplastic elastomer is a fourth styrene-ethylene-butene-styrene block copolymer.
106. The assembly of claim 104 wherein the fifth thermoplastic elastomer is selected from the group consisting of a fifth styrene and hydrocarbon copolymer.
107. The assembly of claim 106 wherein the fifth styrene and hydrocarbon copolymer is selected from the group of polymer structures consisting of diblock, triblock, and star block copolymers.
108. The assembly of claim 107 wherein the fifth thermoplastic elastomer is a fifth styrene-ethylene-butene-styrene block copolymer.
109. The assembly of claim 107 wherein the fifth thermoplastic elastomer is functionalized with a group selected from the group consisting of carboxylic acid, esters of carboxylic acids, anhydrides of carboxylic acids, epoxides, and carbon monoxide.
110. The assembly of claim 109 wherein the fifth thermoplastic elastomer is maleic anhydride functionalized.
111. The assembly of claim 107 wherein the first polyolefin, the third polyolefin, the fourth polyolefin and the fifth polyolefin are propylene copolymerized with ethylene, the ethylene being from about 1% to about 8% by weight of the copolymer, and the second polyolefin and the sixth polyolefin are ethylene and α-olefin copolymers wherein the α-olefin has from 4 to 8 carbons.
US11/079,767 2001-01-08 2005-03-14 Port tube and closure composition, structure and assembly for a flowale material container Abandoned US20050158499A1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US11/079,767 US20050158499A1 (en) 2001-01-08 2005-03-14 Port tube and closure composition, structure and assembly for a flowale material container

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US09/756,490 US6869653B2 (en) 2001-01-08 2001-01-08 Port tube closure assembly
US11/079,767 US20050158499A1 (en) 2001-01-08 2005-03-14 Port tube and closure composition, structure and assembly for a flowale material container

Related Parent Applications (1)

Application Number Title Priority Date Filing Date
US09/756,490 Division US6869653B2 (en) 2001-01-08 2001-01-08 Port tube closure assembly

Publications (1)

Publication Number Publication Date
US20050158499A1 true US20050158499A1 (en) 2005-07-21

Family

ID=25043721

Family Applications (3)

Application Number Title Priority Date Filing Date
US09/756,490 Expired - Lifetime US6869653B2 (en) 2001-01-08 2001-01-08 Port tube closure assembly
US11/042,651 Expired - Fee Related US7550185B2 (en) 2001-01-08 2005-01-24 Port tube and closure composition, structure and assembly for a flowable material container
US11/079,767 Abandoned US20050158499A1 (en) 2001-01-08 2005-03-14 Port tube and closure composition, structure and assembly for a flowale material container

Family Applications Before (2)

Application Number Title Priority Date Filing Date
US09/756,490 Expired - Lifetime US6869653B2 (en) 2001-01-08 2001-01-08 Port tube closure assembly
US11/042,651 Expired - Fee Related US7550185B2 (en) 2001-01-08 2005-01-24 Port tube and closure composition, structure and assembly for a flowable material container

Country Status (18)

Country Link
US (3) US6869653B2 (en)
EP (1) EP1353793B1 (en)
JP (2) JP4739649B2 (en)
KR (1) KR100820988B1 (en)
CN (1) CN1230293C (en)
AT (1) ATE430021T1 (en)
AU (1) AU2002243476B2 (en)
BR (1) BR0206351B1 (en)
CA (1) CA2431989C (en)
CR (1) CR7018A (en)
DE (1) DE60232132D1 (en)
ES (1) ES2325806T3 (en)
IL (5) IL156503A0 (en)
MX (1) MXPA03006106A (en)
PL (2) PL202650B1 (en)
RU (1) RU2277476C2 (en)
WO (1) WO2002053359A1 (en)
ZA (1) ZA200304850B (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20090105684A1 (en) * 2007-10-23 2009-04-23 Baxter International Inc. Medication port for medical fluid container
US20090246434A1 (en) * 2008-03-31 2009-10-01 Wintech Polymer Ltd. Multilayer tube
CN103153619A (en) * 2010-09-14 2013-06-12 杜邦泰吉恩胶卷美国有限公司 Thermoformable copolyester laminate

Families Citing this family (43)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6652942B2 (en) * 2001-01-08 2003-11-25 Baxter International Inc. Assembly for a flowable material container
US7249190B2 (en) * 2001-02-09 2007-07-24 Comlet Technologies, Llc. Enhanced data exchange and presentation/communication system
US7390845B2 (en) * 2002-07-26 2008-06-24 Illinois Tool Works Inc Sealing system and process therefor
US7275543B2 (en) * 2002-09-20 2007-10-02 Baxter International Inc. Coupler member for joining dissimilar materials
SE0203871D0 (en) * 2002-12-20 2002-12-20 Delaval Holding Ab Milking Devices
DE10349011A1 (en) 2003-10-17 2005-05-19 Fresenius Medical Care Deutschland Gmbh PVC-free multilayer tubing with improved peel safety for medical purposes, process for its preparation and use
US20050186377A1 (en) * 2004-02-19 2005-08-25 Hurst William S. Solventless plastic bonding of medical devices and container components through infrared heating
JP4596124B2 (en) * 2004-03-09 2010-12-08 藤森工業株式会社 Medical container
SE527446C2 (en) * 2004-06-10 2006-03-07 Delaval Holding Ab milking devices
KR100653407B1 (en) 2004-11-11 2006-12-07 주식회사 메디펙 Port tube for non-PVC bags
DE102004058063A1 (en) * 2004-12-02 2006-06-08 Lanxess Deutschland Gmbh Mixtures of ethylene-vinyl alcohol copolymers and crosslinkable rubbers with reactive groups and their use for the production of shaped articles with good barrier properties
CA2592432A1 (en) * 2004-12-23 2006-07-06 Hospira, Inc. Port closure system for intravenous fluid container
KR100705659B1 (en) * 2005-01-17 2007-04-10 (주)폴리머스넷 Acrylate-based polymer resin
KR100705656B1 (en) * 2005-02-17 2007-04-10 (주)폴리머스넷 Directly Paintable Polypropylene-Based Resin Composition
KR100690975B1 (en) * 2005-02-24 2007-03-09 (주)폴리머스넷 Composition of resin based on polyolefin with improved surface printability
US20070102858A1 (en) * 2005-11-07 2007-05-10 Navigant Biotechnologies, Inc. Clamps and methods for displacing fluid from portions of fluid containers
CN1978963B (en) * 2005-11-29 2011-02-16 青岛三祥科技有限公司 Automotive oil lubricator flexible pipe
WO2007075585A2 (en) 2005-12-16 2007-07-05 Interface Associates, Inc. Multi-layer balloons for medical applications and methods for manufacturing the same
BRPI0708881B1 (en) * 2006-04-06 2018-02-27 Fresenius Medical Care Deutschland Gmbh MEDICAL PIPE
US8557359B2 (en) * 2006-04-12 2013-10-15 Abbott Laboratories Closure for container
KR100866652B1 (en) * 2007-05-18 2008-11-03 (주)폴리머스넷 Polyacrylate-based polymer
ES2739030T3 (en) * 2007-09-28 2020-01-28 Hollister Inc Multi-layer anti-odor barrier tube, and combination of anti-odor barrier tube and anti-odor barrier collection bag
US8936583B2 (en) 2007-09-28 2015-01-20 Hollister Incorporated Multi-layer catheter tubes with odor barrier
US20090093794A1 (en) * 2007-10-03 2009-04-09 Tyco Healthcare Group Lp Bolus tube assembly
US8443824B2 (en) * 2007-10-09 2013-05-21 Fenwal, Inc. Fluid flow controller
EP2151319A1 (en) * 2008-08-08 2010-02-10 PolyCine GmbH Plug to seal a medicinal system
EP2519580B1 (en) 2009-12-29 2015-03-04 Saint-gobain Performance Plastics Corporation A flexible tubing material and method of forming the material
JP5632226B2 (en) * 2010-07-30 2014-11-26 株式会社細川洋行 Medical multilayer tube and medical infusion bag
WO2013106605A1 (en) 2012-01-11 2013-07-18 Terumo Bct Biotechnologies, Llc Slidable clamp for port isolation
WO2013184517A1 (en) 2012-06-06 2013-12-12 Saint-Gobain Performance Plastics Corporation Thermoplastic elastomer tubing and method to make and use same
KR101260463B1 (en) 2012-08-07 2013-05-06 주식회사 폴리사이언텍 Pvc-free medical tubes, moulding parts and medical supplies produced therefrom
WO2014025142A1 (en) * 2012-08-07 2014-02-13 주식회사 폴리사이언텍 Polyvinyl chloride-free medical tube, and molded articles and medical supplies produced therewith
KR101260476B1 (en) 2012-08-07 2013-05-06 주식회사 폴리사이언텍 Pvc-free medical tubes, moulding parts and medical supplies produced therefrom
KR101292325B1 (en) 2013-01-28 2013-08-01 주식회사 폴리사이언텍 Pvc-free medical moulding parts and medical supplies produced therefrom
US9062803B2 (en) * 2013-03-22 2015-06-23 Tekni-Plax, Inc. Extrudable multilayer tubing
US10251770B2 (en) 2014-01-03 2019-04-09 Hollister Incorporated Lubricated valve for ostomy pouch
US20160030728A1 (en) * 2014-07-31 2016-02-04 Tekni-Plex, Inc. Extrudable tubing and solvent bonded fitting for delivery of medicinal fluids
WO2016165731A1 (en) 2015-04-13 2016-10-20 N.V. Nutricia Tube for a medical container
CN105585760A (en) * 2016-01-25 2016-05-18 蚌埠市万达塑料制品有限公司 Top sealing ring of plastic thermos bottle stopper
EP3735349A4 (en) * 2018-01-05 2021-08-04 Baxter International Inc. Multi-layer articles and methods for producing the same
CN109666216A (en) * 2018-12-17 2019-04-23 会通新材料(上海)有限公司 A kind of long glass fiber-reinforced polypropylene/polyamide alloy material and preparation method thereof of high-intensitive, low smell
CN111909531B (en) * 2019-05-09 2022-05-20 中国石油化工股份有限公司 Polyolefin composition and pallet and method for making the same
CN110218459A (en) * 2019-05-29 2019-09-10 江苏中利集团股份有限公司 A kind of TPE insulating materials

Citations (99)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2234237A (en) * 1936-10-31 1941-03-11 Herbert E Feist Coating
US2342215A (en) * 1942-08-03 1944-02-22 Harold N Perelson Dispensing and sealing stopper
US2562389A (en) * 1945-11-03 1951-07-31 Shellmar Products Corp Bag and method
US2894510A (en) * 1954-02-25 1959-07-14 Fenwal Lab Inc Sealing closures for fluid containers
US2940444A (en) * 1958-10-06 1960-06-14 Abbott Lab Container
US3030952A (en) * 1956-12-24 1962-04-24 Baxter Don Inc Solution administration device and method of forming the same
US3442737A (en) * 1963-12-16 1969-05-06 Petro Tex Chem Corp Bonding poly(butene-1)
US3514359A (en) * 1965-10-11 1970-05-26 Huels Chemische Werke Ag Process of uniting objects of polybutene-(1)
US3589422A (en) * 1969-03-17 1971-06-29 Baxter Laboratories Inc Sealed bag for liquids
US3642047A (en) * 1968-11-21 1972-02-15 Investrop Ag Laminated container of thermoplastic and nonthermoplastic materials with nipples
US3746001A (en) * 1971-10-20 1973-07-17 Baxter Laboratories Inc Pierceable access port for parenteral solution containers
US3788374A (en) * 1972-01-26 1974-01-29 Jintan Terumo Co Parenteral solution bag
US3861973A (en) * 1973-02-27 1975-01-21 Rilsan Corp Polyamide hose and preparation thereof
US3866631A (en) * 1972-07-06 1975-02-18 Imp Eastman Corp Hose construction
US3869338A (en) * 1972-03-14 1975-03-04 Union Carbide Corp Tubing for cryogenic use
US3900640A (en) * 1973-10-29 1975-08-19 Amerace Corp Hollow, multi-layered, cross-linked plastic structures and process for producing same
US3951148A (en) * 1974-05-29 1976-04-20 Pharmachem Corporation Blood component storage bag and glycerolizing set therefor
US3973026A (en) * 1975-02-05 1976-08-03 Societa Italo-Britannica L. Manetti-H. Roberts & C. Inhibitor of blood plate aggregation
US4137117A (en) * 1977-03-10 1979-01-30 American Hospital Supply Corporation Method of making a solvent-bonded joint
US4187893A (en) * 1978-07-19 1980-02-12 Abbott Laboratories Combined additive and administration port for a container
US4201208A (en) * 1977-11-30 1980-05-06 Abbott Laboratories Sterile connecting device
US4327726A (en) * 1979-08-15 1982-05-04 Baxter Travenol Laboratories, Inc. Connector member for dissimilar materials
US4340049A (en) * 1979-10-18 1982-07-20 Baxter Travenol Laboratories, Inc. Breakaway valve
US4386622A (en) * 1979-10-18 1983-06-07 Baxter Travenol Laboratories, Inc. Breakaway valve
US4393909A (en) * 1981-12-28 1983-07-19 Baxter Travenol Laboratories, Inc. Universal administration port
US4441538A (en) * 1979-12-26 1984-04-10 Abbott Laboratories Flexible container with integral ports and diaphragm
US4465488A (en) * 1981-03-23 1984-08-14 Baxter Travenol Laboratories, Inc. Collapsible multi-chamber medical fluid container
US4516977A (en) * 1983-02-17 1985-05-14 Fresenius, Ag Storage bag
US4523691A (en) * 1983-04-08 1985-06-18 Abbott Laboratories Port structure for I.V. container
US4524880A (en) * 1983-07-29 1985-06-25 Pharmacia Ab Closure device
US4567999A (en) * 1981-05-07 1986-02-04 International Nutritional Research Institute Ab Self-adhesive connecting device
US4576602A (en) * 1984-02-08 1986-03-18 Abbott Laboratories Blow molded container with integral administration port
US4578074A (en) * 1982-07-22 1986-03-25 Medistad Holland V.V. Infusion liquid pouch
US4586928A (en) * 1984-10-09 1986-05-06 Miles Laboratories, Inc. Pivoting frangible valve for plastic bags
US4588777A (en) * 1982-10-21 1986-05-13 Dainippon Plastics Co., Ltd. Synthetic resin composition
US4588396A (en) * 1982-10-22 1986-05-13 Stroebel Maurice G Apparatus for gravity feed of liquid under constant hydrostatic pressure
US4596573A (en) * 1983-01-08 1986-06-24 The Boots Company P.L.C. Container
US4599276A (en) * 1983-11-09 1986-07-08 W. R. Grace & Co., Cryovac Div. Heat-sterilizable laminate films
US4607671A (en) * 1984-08-21 1986-08-26 Baxter Travenol Laboratories, Inc. Reconstitution device
US4636204A (en) * 1982-04-13 1987-01-13 Gambro Lundia Ab Coupling for the connection of flexible tubes and the like
US4666549A (en) * 1985-08-29 1987-05-19 Phillips Petroleum Company Polymer welding process and composition
US4676775A (en) * 1984-06-27 1987-06-30 David M. Roxe Fluid administration apparatus and method
US4723956A (en) * 1984-09-14 1988-02-09 Baxter Travenol Laboratories, Inc. Port free container
US4808179A (en) * 1984-05-09 1989-02-28 Ab Akerlund & Rausing Container device and a method for manufacturing of the device
US4838875A (en) * 1987-12-09 1989-06-13 Somor Andrew T Method and apparatus for dealing with intravenous fluids
US4857129A (en) * 1987-07-31 1989-08-15 Plastic Welding Technologies, Inc. Method of bonding thermoplastic material using radio frequency energy
US4917684A (en) * 1986-09-01 1990-04-17 Japan Medical Supply Co., Ltd. Protective cover for inlet/outlet ports of the plastic bag used for medical purpose
US4950347A (en) * 1986-01-12 1990-08-21 Nissho Corporation Method for welding thermoplastic resin
US5011719A (en) * 1985-11-29 1991-04-30 American National Can Company Polymeric compositions and films
US5084042A (en) * 1990-06-29 1992-01-28 Mcgaw, Inc. Medical solution container outlet port with improved pierceable diaphragm
US5088995A (en) * 1990-06-22 1992-02-18 Baxter International Inc. Port and closure assembly including a resealing injection site for a container
US5114768A (en) * 1988-06-02 1992-05-19 Hewlett-Packard Company Surfaces with reduced protein interactions
US5122126A (en) * 1989-05-17 1992-06-16 Terumo Kabushiki Kaisha Nozzle member provided with sealing membrane
US5125919A (en) * 1988-08-31 1992-06-30 Clintec Nutrition Company Wedge-shaped port for flexible containers
US5137527A (en) * 1990-09-20 1992-08-11 Clintec Nutrition Co. Enteral-specific spike/bag port system
US5188628A (en) * 1990-11-06 1993-02-23 Sandoz Ltd. Closure device for enteral fluid containers
US5222950A (en) * 1990-07-16 1993-06-29 Eisenberg Melvin I Quick release tamper evident closure device
US5297599A (en) * 1991-03-19 1994-03-29 Hoffmann-Laroche Inc. Closure device for sealing reagent containers in an automatic pipetting system
US5303751A (en) * 1991-10-04 1994-04-19 Fresenius Ag Spiked bag packaging system
US5308347A (en) * 1991-09-18 1994-05-03 Fujisawa Pharmaceutical Co., Ltd. Transfusion device
US5330464A (en) * 1992-03-11 1994-07-19 Baxter International Inc. Reliable breakable closure mechanism
US5334180A (en) * 1993-04-01 1994-08-02 Abbott Laboratories Sterile formed, filled and sealed flexible container
US5336351A (en) * 1992-07-14 1994-08-09 Tuf-Tite, Inc. Method for connecting a pipe connector to a hard plastic pipe
US5342345A (en) * 1993-01-04 1994-08-30 Denco, Inc. Solution bag with plastic connecting tube
US5342346A (en) * 1992-04-10 1994-08-30 Nissho Corporation Fluid container
US5391150A (en) * 1992-12-28 1995-02-21 Richmond; Frank IV bag with needleless connector ports
US5395365A (en) * 1993-03-22 1995-03-07 Automatic Liquid Packaging, Inc. Container with pierceable and/or collapsible features
US5416142A (en) * 1991-12-17 1995-05-16 Oatey Company Method of bonding and bonding compositions
US5423794A (en) * 1993-09-28 1995-06-13 Abbott Laboratories Intravenous container with siphoning port
US5514123A (en) * 1993-04-01 1996-05-07 Abbott Laboratories Sterile formed, filled and sealed flexible container
US5520641A (en) * 1995-02-06 1996-05-28 Minnesota Mining And Manufacturing Company IV injection and sampling site having septum with multiple openings
US5529821A (en) * 1992-06-29 1996-06-25 Terumo Kabushiki Kaisha Container for storing blood or blood component
US5540674A (en) * 1993-09-28 1996-07-30 Abbott Laboratories Solution container with dual use access port
US5601889A (en) * 1992-05-29 1997-02-11 Ferro Corporation Radio frequency weldable polymer articles
US5618883A (en) * 1995-06-07 1997-04-08 Avery Dennison Corporation Styrene ethylene-butylene and ethylene-propylene block copolymer hot melt pressure sensitive adhesives
US5645904A (en) * 1991-12-11 1997-07-08 Baxter International Inc. Method and compositions that render materials RF responsive
US5728087A (en) * 1996-07-30 1998-03-17 Bracco Diagnostics, Inc. Universal flexible plastic container with multiple access ports of inverted Y shape configuration
US5733619A (en) * 1992-01-30 1998-03-31 Baxter International Inc. Multilayer coextruded material for medical grade products and products made therefrom
US5744250A (en) * 1993-12-29 1998-04-28 E. I. Du Pont De Nemours And Company Adhesion compositions for multilayer structures
US5772880A (en) * 1993-09-14 1998-06-30 Baxter International, Inc. Container with a tangential port
US5772652A (en) * 1997-05-14 1998-06-30 Comar, Inc. Stab cap for a vial having a puncturable seal
US5776116A (en) * 1983-01-24 1998-07-07 Icu Medical, Inc. Medical connector
US5777043A (en) * 1997-03-05 1998-07-07 Shell Oil Company Sealant formulations containing high vinyl content hydrogenated styrene-butadiene-styrene block copolymers
US5779832A (en) * 1996-11-25 1998-07-14 W. R. Grace & Co.-Conn. Method and apparatus for making a peelable film
US5928744A (en) * 1995-09-16 1999-07-27 Fresenius Ag PVC-free multilayer tube for medical purposes, process for the production thereof and use
US5928740A (en) * 1997-02-28 1999-07-27 Viskase Corporation Thermoplastic C2 -α-olefin copolymer blends and films
US6019751A (en) * 1998-01-20 2000-02-01 Bracco Research Usa Universal connector and a medical container
US6019750A (en) * 1997-12-04 2000-02-01 Baxter International Inc. Sliding reconstitution device with seal
US6022344A (en) * 1997-12-04 2000-02-08 Npbi International B.V. Cryopreservation bag
US6027776A (en) * 1995-03-22 2000-02-22 Cryovac, Inc. Multilayer films for packaging and administering medical solutions
US6083194A (en) * 1995-06-07 2000-07-04 Icu Medical, Inc. Medical connector
US6179821B1 (en) * 1998-06-18 2001-01-30 Glenn A. Caspary Membrane port for a container
US6184280B1 (en) * 1995-10-23 2001-02-06 Mitsubishi Materials Corporation Electrically conductive polymer composition
US6408892B1 (en) * 1998-12-28 2002-06-25 Mitsubishi Jidosha Kogyo Kabushiki Kaisha Car vacuum hose
US6548181B2 (en) * 1996-12-23 2003-04-15 Dsm N.V. Flexible polyamide composition
US6593428B2 (en) * 2000-09-19 2003-07-15 E. I. Dupont De Nemours And Company Syndiotactic polystyrene alloy compositions
US20040030057A1 (en) * 2000-06-16 2004-02-12 Nicolangelo Peduto Modified polyamides, polyamide compositions, and method for making same
US20040048981A1 (en) * 2000-04-12 2004-03-11 Park Jung Hoon Thermoplastic polymeric compositions
US6764761B2 (en) * 2002-05-24 2004-07-20 Baxter International Inc. Membrane material for automated dialysis system

Family Cites Families (54)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1966795A (en) * 1933-02-23 1934-07-17 Thomas T Garrison Thrust bearing
US2324237A (en) 1941-03-19 1943-07-13 Reichel John Container
US2808829A (en) 1955-04-06 1957-10-08 Cutter Lab Blood transfusion equipment
US3161310A (en) 1960-10-14 1964-12-15 Baxter Don Inc Parenteral solution container
DE1604675C3 (en) 1966-03-24 1973-11-15 Peralt Anstalt, Vaduz Device for the edge-side Ver bind two flat plastic sheeting
US3928110A (en) 1974-03-11 1975-12-23 Goodyear Tire & Rubber Film bonding using a solvent saturated cloth wick
US3911051A (en) 1974-04-25 1975-10-07 Richardson Co Cross-linked ultra high molecular weight polyethylene and S-B copolymer composition and process for molding
US3963026A (en) 1974-11-19 1976-06-15 Pharmachem Corporation Blood component storage bag and glycerolizing set therefor
US3991912A (en) 1975-01-23 1976-11-16 Ricardo Hurtado Soto Flexible package with counter-pressure dispenser
US3978859A (en) 1975-01-23 1976-09-07 Cutter Laboratories, Inc. Closure member for pierceable access ports
US3986507A (en) 1975-04-16 1976-10-19 Inpaco Parenteral container
US4049034A (en) 1976-07-14 1977-09-20 Baxter Travenol Laboratories, Inc. Attaching means and method for attaching flexible tubing to a plastic container
US4240481A (en) 1979-03-05 1980-12-23 Baxter Travenol Laboratories, Inc. Seal for flexible container having flexible, generally conical portions
JPS5841964Y2 (en) 1979-05-18 1983-09-22 テルモ株式会社 plastic pharmaceutical liquid containers
US4547900A (en) 1979-12-26 1985-10-15 Abbott Laboratories Flexible container with integral ports and diaphragm
US4303067A (en) 1980-01-21 1981-12-01 American Hospital Supply Corporation Medical liquid bag having an improved additive port
IT8034810V0 (en) 1980-01-22 1980-01-22 Lena Paolo SYNTHETIC BAG CONTAINER FOR HUMAN BLOOD AND ITS FRACTIONS, PERFUSIONAL SOLUTIONS, DIALYTIC SOLUTIONS AND FOR FOOD AND CHEMICAL LIQUIDS IN GENERAL
US4412573A (en) 1981-12-28 1983-11-01 Baxter Travenol Laboratories, Inc. Injection site
US4484916A (en) 1982-01-20 1984-11-27 American Hospital Supply Corporation Medical solution container and port construction
JPS58155867A (en) 1982-03-12 1983-09-16 テルモ株式会社 Drill needle and medical container with drill needle
US4479989A (en) 1982-12-02 1984-10-30 Cutter Laboratories, Inc. Flexible container material
US4632673A (en) 1983-06-15 1986-12-30 Hantaaki Oy Pierceable port for containers
SE442264B (en) 1983-12-23 1985-12-16 Bengt Gustavsson AMPOULE
US4610374A (en) 1984-10-29 1986-09-09 Dougherty Brothers Company Apparatus for mixing flowable materials in sealed containers
US4966795A (en) 1985-11-29 1990-10-30 American National Can Company Multiple layer sheet structures and package
US4869384A (en) 1988-01-12 1989-09-26 International Medication Systems Limited Package for toxic and dangerous drugs
DE68928990T2 (en) 1988-06-02 1999-12-02 Piero Marrucchi Device for treating and transferring substances between closed rooms
US5251982A (en) 1988-07-08 1993-10-12 Ab Tetra Pak Discharging device for a packaging container
US4969883A (en) 1989-01-03 1990-11-13 Gilbert Michael D Medicament vial end cap membrane piercing device
US5259894A (en) 1990-01-26 1993-11-09 Sampson Richard K Method for solvent bonding non-porous materials to automatically create variable bond characteristics
US5071413A (en) 1990-06-13 1991-12-10 Utterberg David S Universal connector
US5167816A (en) 1990-08-20 1992-12-01 Abbott Laboratories Sterile coupling device for drug container
US5259843A (en) 1991-11-14 1993-11-09 Kawasumi Laboratories Inc. Medical connector for attaching to liquid introducing tube
ZA931680B (en) * 1992-03-30 1993-10-05 Grace W R & Co Medical solution tubing
US5356709A (en) * 1992-05-14 1994-10-18 Baxter International, Inc. Non-PVC coextruded medical grade port tubing
US5810398A (en) * 1992-10-02 1998-09-22 Pall Corporation Fluid delivery systems and methods and assemblies for making connections
DE4315003A1 (en) * 1993-05-06 1994-11-10 Theka Flex Produktions Und Han Thermoplastic elastomer compound
EP0712354B1 (en) * 1993-08-06 1999-01-13 Minnesota Mining And Manufacturing Company Multilayered tubing
US5998019A (en) * 1993-11-16 1999-12-07 Baxter International Inc. Multi-layered polymer structure for medical products
US5458593A (en) 1993-11-24 1995-10-17 Bayer Corporation Dockable bag system and method
DE19536546A1 (en) * 1994-03-29 1997-04-03 Fresenius Ag Heat-sterilisable pouch with non-adhering inner surfaces for medicinal use
JP3191054B2 (en) * 1994-06-01 2001-07-23 ザ・ダウ・ケミカル・カンパニー Thermoplastic blend composition
WO1995035347A1 (en) * 1994-06-17 1995-12-28 Alliedsignal Inc. Articles comprising extruded polyamide-grafted low density polyethylene blends
JPH0852196A (en) * 1994-08-09 1996-02-27 Material Eng Tech Lab Inc Transfusion container having connecting port for medicine
DE19540437B4 (en) * 1994-10-31 2004-04-01 Toyoda Gosei Co., Ltd. High-gloss molded part made of resin
US5584825A (en) * 1994-12-01 1996-12-17 Isolyser Co., Inc. Closure delivery system
DE19534413C1 (en) * 1995-09-16 1997-05-28 Fresenius Ag Connection arrangement and method for connecting two individual parts of a medical system
US6617008B1 (en) * 1996-02-22 2003-09-09 Idemitsu Petrochemical Co., Ltd. Decorative film or sheet, and decorative material and building material made by using the same
US6127009A (en) * 1996-05-08 2000-10-03 Pactiv Corporation Dispenser unit, process for manufacturing the same and its use
US6132413A (en) * 1998-03-06 2000-10-17 Baxter International Inc. Breakable cannula assemblies and methods for manipulating them
US6451446B1 (en) * 1998-05-21 2002-09-17 Dow Global Technologies Inc. Polypropylene/polystyrene multilayer film structures
JP2001261905A (en) * 2000-03-21 2001-09-26 Mitsui Chemicals Inc Modified polypropylene composition and laminate using the composition
US6623399B2 (en) * 2001-12-28 2003-09-23 Dow Corning Corporation Traction fluids
ATE447423T1 (en) * 2002-03-04 2009-11-15 Terumo Corp MEDICAL HOSE AND EXTRUSION NOZZLE FOR PRODUCING IT

Patent Citations (99)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2234237A (en) * 1936-10-31 1941-03-11 Herbert E Feist Coating
US2342215A (en) * 1942-08-03 1944-02-22 Harold N Perelson Dispensing and sealing stopper
US2562389A (en) * 1945-11-03 1951-07-31 Shellmar Products Corp Bag and method
US2894510A (en) * 1954-02-25 1959-07-14 Fenwal Lab Inc Sealing closures for fluid containers
US3030952A (en) * 1956-12-24 1962-04-24 Baxter Don Inc Solution administration device and method of forming the same
US2940444A (en) * 1958-10-06 1960-06-14 Abbott Lab Container
US3442737A (en) * 1963-12-16 1969-05-06 Petro Tex Chem Corp Bonding poly(butene-1)
US3514359A (en) * 1965-10-11 1970-05-26 Huels Chemische Werke Ag Process of uniting objects of polybutene-(1)
US3642047A (en) * 1968-11-21 1972-02-15 Investrop Ag Laminated container of thermoplastic and nonthermoplastic materials with nipples
US3589422A (en) * 1969-03-17 1971-06-29 Baxter Laboratories Inc Sealed bag for liquids
US3746001A (en) * 1971-10-20 1973-07-17 Baxter Laboratories Inc Pierceable access port for parenteral solution containers
US3788374A (en) * 1972-01-26 1974-01-29 Jintan Terumo Co Parenteral solution bag
US3869338A (en) * 1972-03-14 1975-03-04 Union Carbide Corp Tubing for cryogenic use
US3866631A (en) * 1972-07-06 1975-02-18 Imp Eastman Corp Hose construction
US3861973A (en) * 1973-02-27 1975-01-21 Rilsan Corp Polyamide hose and preparation thereof
US3900640A (en) * 1973-10-29 1975-08-19 Amerace Corp Hollow, multi-layered, cross-linked plastic structures and process for producing same
US3951148A (en) * 1974-05-29 1976-04-20 Pharmachem Corporation Blood component storage bag and glycerolizing set therefor
US3973026A (en) * 1975-02-05 1976-08-03 Societa Italo-Britannica L. Manetti-H. Roberts & C. Inhibitor of blood plate aggregation
US4137117A (en) * 1977-03-10 1979-01-30 American Hospital Supply Corporation Method of making a solvent-bonded joint
US4201208A (en) * 1977-11-30 1980-05-06 Abbott Laboratories Sterile connecting device
US4187893A (en) * 1978-07-19 1980-02-12 Abbott Laboratories Combined additive and administration port for a container
US4327726A (en) * 1979-08-15 1982-05-04 Baxter Travenol Laboratories, Inc. Connector member for dissimilar materials
US4340049A (en) * 1979-10-18 1982-07-20 Baxter Travenol Laboratories, Inc. Breakaway valve
US4386622A (en) * 1979-10-18 1983-06-07 Baxter Travenol Laboratories, Inc. Breakaway valve
US4441538A (en) * 1979-12-26 1984-04-10 Abbott Laboratories Flexible container with integral ports and diaphragm
US4465488A (en) * 1981-03-23 1984-08-14 Baxter Travenol Laboratories, Inc. Collapsible multi-chamber medical fluid container
US4567999A (en) * 1981-05-07 1986-02-04 International Nutritional Research Institute Ab Self-adhesive connecting device
US4393909A (en) * 1981-12-28 1983-07-19 Baxter Travenol Laboratories, Inc. Universal administration port
US4636204A (en) * 1982-04-13 1987-01-13 Gambro Lundia Ab Coupling for the connection of flexible tubes and the like
US4578074A (en) * 1982-07-22 1986-03-25 Medistad Holland V.V. Infusion liquid pouch
US4588777A (en) * 1982-10-21 1986-05-13 Dainippon Plastics Co., Ltd. Synthetic resin composition
US4588396A (en) * 1982-10-22 1986-05-13 Stroebel Maurice G Apparatus for gravity feed of liquid under constant hydrostatic pressure
US4596573A (en) * 1983-01-08 1986-06-24 The Boots Company P.L.C. Container
US5776116A (en) * 1983-01-24 1998-07-07 Icu Medical, Inc. Medical connector
US4516977A (en) * 1983-02-17 1985-05-14 Fresenius, Ag Storage bag
US4523691A (en) * 1983-04-08 1985-06-18 Abbott Laboratories Port structure for I.V. container
US4524880A (en) * 1983-07-29 1985-06-25 Pharmacia Ab Closure device
US4599276A (en) * 1983-11-09 1986-07-08 W. R. Grace & Co., Cryovac Div. Heat-sterilizable laminate films
US4576602A (en) * 1984-02-08 1986-03-18 Abbott Laboratories Blow molded container with integral administration port
US4808179A (en) * 1984-05-09 1989-02-28 Ab Akerlund & Rausing Container device and a method for manufacturing of the device
US4676775A (en) * 1984-06-27 1987-06-30 David M. Roxe Fluid administration apparatus and method
US4607671A (en) * 1984-08-21 1986-08-26 Baxter Travenol Laboratories, Inc. Reconstitution device
US4723956A (en) * 1984-09-14 1988-02-09 Baxter Travenol Laboratories, Inc. Port free container
US4586928A (en) * 1984-10-09 1986-05-06 Miles Laboratories, Inc. Pivoting frangible valve for plastic bags
US4666549A (en) * 1985-08-29 1987-05-19 Phillips Petroleum Company Polymer welding process and composition
US5011719A (en) * 1985-11-29 1991-04-30 American National Can Company Polymeric compositions and films
US4950347A (en) * 1986-01-12 1990-08-21 Nissho Corporation Method for welding thermoplastic resin
US4917684A (en) * 1986-09-01 1990-04-17 Japan Medical Supply Co., Ltd. Protective cover for inlet/outlet ports of the plastic bag used for medical purpose
US4857129A (en) * 1987-07-31 1989-08-15 Plastic Welding Technologies, Inc. Method of bonding thermoplastic material using radio frequency energy
US4838875A (en) * 1987-12-09 1989-06-13 Somor Andrew T Method and apparatus for dealing with intravenous fluids
US5114768A (en) * 1988-06-02 1992-05-19 Hewlett-Packard Company Surfaces with reduced protein interactions
US5125919A (en) * 1988-08-31 1992-06-30 Clintec Nutrition Company Wedge-shaped port for flexible containers
US5122126A (en) * 1989-05-17 1992-06-16 Terumo Kabushiki Kaisha Nozzle member provided with sealing membrane
US5088995A (en) * 1990-06-22 1992-02-18 Baxter International Inc. Port and closure assembly including a resealing injection site for a container
US5084042A (en) * 1990-06-29 1992-01-28 Mcgaw, Inc. Medical solution container outlet port with improved pierceable diaphragm
US5222950A (en) * 1990-07-16 1993-06-29 Eisenberg Melvin I Quick release tamper evident closure device
US5137527A (en) * 1990-09-20 1992-08-11 Clintec Nutrition Co. Enteral-specific spike/bag port system
US5188628A (en) * 1990-11-06 1993-02-23 Sandoz Ltd. Closure device for enteral fluid containers
US5297599A (en) * 1991-03-19 1994-03-29 Hoffmann-Laroche Inc. Closure device for sealing reagent containers in an automatic pipetting system
US5308347A (en) * 1991-09-18 1994-05-03 Fujisawa Pharmaceutical Co., Ltd. Transfusion device
US5303751A (en) * 1991-10-04 1994-04-19 Fresenius Ag Spiked bag packaging system
US5645904A (en) * 1991-12-11 1997-07-08 Baxter International Inc. Method and compositions that render materials RF responsive
US5416142A (en) * 1991-12-17 1995-05-16 Oatey Company Method of bonding and bonding compositions
US5733619A (en) * 1992-01-30 1998-03-31 Baxter International Inc. Multilayer coextruded material for medical grade products and products made therefrom
US5330464A (en) * 1992-03-11 1994-07-19 Baxter International Inc. Reliable breakable closure mechanism
US5342346A (en) * 1992-04-10 1994-08-30 Nissho Corporation Fluid container
US5601889A (en) * 1992-05-29 1997-02-11 Ferro Corporation Radio frequency weldable polymer articles
US5529821A (en) * 1992-06-29 1996-06-25 Terumo Kabushiki Kaisha Container for storing blood or blood component
US5336351A (en) * 1992-07-14 1994-08-09 Tuf-Tite, Inc. Method for connecting a pipe connector to a hard plastic pipe
US5391150A (en) * 1992-12-28 1995-02-21 Richmond; Frank IV bag with needleless connector ports
US5342345A (en) * 1993-01-04 1994-08-30 Denco, Inc. Solution bag with plastic connecting tube
US5395365A (en) * 1993-03-22 1995-03-07 Automatic Liquid Packaging, Inc. Container with pierceable and/or collapsible features
US5334180A (en) * 1993-04-01 1994-08-02 Abbott Laboratories Sterile formed, filled and sealed flexible container
US5514123A (en) * 1993-04-01 1996-05-07 Abbott Laboratories Sterile formed, filled and sealed flexible container
US5772880A (en) * 1993-09-14 1998-06-30 Baxter International, Inc. Container with a tangential port
US5540674A (en) * 1993-09-28 1996-07-30 Abbott Laboratories Solution container with dual use access port
US5423794A (en) * 1993-09-28 1995-06-13 Abbott Laboratories Intravenous container with siphoning port
US5744250A (en) * 1993-12-29 1998-04-28 E. I. Du Pont De Nemours And Company Adhesion compositions for multilayer structures
US5520641A (en) * 1995-02-06 1996-05-28 Minnesota Mining And Manufacturing Company IV injection and sampling site having septum with multiple openings
US6027776A (en) * 1995-03-22 2000-02-22 Cryovac, Inc. Multilayer films for packaging and administering medical solutions
US5618883A (en) * 1995-06-07 1997-04-08 Avery Dennison Corporation Styrene ethylene-butylene and ethylene-propylene block copolymer hot melt pressure sensitive adhesives
US6083194A (en) * 1995-06-07 2000-07-04 Icu Medical, Inc. Medical connector
US5928744A (en) * 1995-09-16 1999-07-27 Fresenius Ag PVC-free multilayer tube for medical purposes, process for the production thereof and use
US6184280B1 (en) * 1995-10-23 2001-02-06 Mitsubishi Materials Corporation Electrically conductive polymer composition
US5728087A (en) * 1996-07-30 1998-03-17 Bracco Diagnostics, Inc. Universal flexible plastic container with multiple access ports of inverted Y shape configuration
US5779832A (en) * 1996-11-25 1998-07-14 W. R. Grace & Co.-Conn. Method and apparatus for making a peelable film
US6548181B2 (en) * 1996-12-23 2003-04-15 Dsm N.V. Flexible polyamide composition
US5928740A (en) * 1997-02-28 1999-07-27 Viskase Corporation Thermoplastic C2 -α-olefin copolymer blends and films
US5777043A (en) * 1997-03-05 1998-07-07 Shell Oil Company Sealant formulations containing high vinyl content hydrogenated styrene-butadiene-styrene block copolymers
US5772652A (en) * 1997-05-14 1998-06-30 Comar, Inc. Stab cap for a vial having a puncturable seal
US6022344A (en) * 1997-12-04 2000-02-08 Npbi International B.V. Cryopreservation bag
US6019750A (en) * 1997-12-04 2000-02-01 Baxter International Inc. Sliding reconstitution device with seal
US6019751A (en) * 1998-01-20 2000-02-01 Bracco Research Usa Universal connector and a medical container
US6179821B1 (en) * 1998-06-18 2001-01-30 Glenn A. Caspary Membrane port for a container
US6408892B1 (en) * 1998-12-28 2002-06-25 Mitsubishi Jidosha Kogyo Kabushiki Kaisha Car vacuum hose
US20040048981A1 (en) * 2000-04-12 2004-03-11 Park Jung Hoon Thermoplastic polymeric compositions
US20040030057A1 (en) * 2000-06-16 2004-02-12 Nicolangelo Peduto Modified polyamides, polyamide compositions, and method for making same
US6593428B2 (en) * 2000-09-19 2003-07-15 E. I. Dupont De Nemours And Company Syndiotactic polystyrene alloy compositions
US6764761B2 (en) * 2002-05-24 2004-07-20 Baxter International Inc. Membrane material for automated dialysis system

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20090105684A1 (en) * 2007-10-23 2009-04-23 Baxter International Inc. Medication port for medical fluid container
US20090246434A1 (en) * 2008-03-31 2009-10-01 Wintech Polymer Ltd. Multilayer tube
US8210213B2 (en) * 2008-03-31 2012-07-03 Wintech Polymer Ltd. Multilayer tube
CN103153619A (en) * 2010-09-14 2013-06-12 杜邦泰吉恩胶卷美国有限公司 Thermoformable copolyester laminate
US10954054B2 (en) 2010-09-14 2021-03-23 Dupont Teijin Films U.S. Limited Partnership Thermoformable copolyester laminate

Also Published As

Publication number Publication date
EP1353793B1 (en) 2009-04-29
EP1353793A1 (en) 2003-10-22
PL368643A1 (en) 2005-04-04
JP2008220973A (en) 2008-09-25
KR100820988B1 (en) 2008-04-08
ZA200304850B (en) 2004-08-19
PL202650B1 (en) 2009-07-31
US20050123703A1 (en) 2005-06-09
IL156503A0 (en) 2004-01-04
US7550185B2 (en) 2009-06-23
IL177174A0 (en) 2006-12-10
IL177175A0 (en) 2006-12-10
JP4739649B2 (en) 2011-08-03
CN1230293C (en) 2005-12-07
ES2325806T3 (en) 2009-09-18
CA2431989A1 (en) 2002-07-11
MXPA03006106A (en) 2004-05-04
AU2002243476B2 (en) 2005-12-22
PL203895B1 (en) 2009-11-30
US20020090476A1 (en) 2002-07-11
ATE430021T1 (en) 2009-05-15
DE60232132D1 (en) 2009-06-10
KR20030069203A (en) 2003-08-25
WO2002053359A1 (en) 2002-07-11
IL177175A (en) 2014-02-27
CA2431989C (en) 2012-07-31
CN1486243A (en) 2004-03-31
US6869653B2 (en) 2005-03-22
BR0206351A (en) 2004-07-20
IL156503A (en) 2007-02-11
JP2004516898A (en) 2004-06-10
IL202202A0 (en) 2010-06-16
CR7018A (en) 2004-03-08
RU2003124568A (en) 2005-01-10
BR0206351B1 (en) 2011-12-27
IL177174A (en) 2014-07-31
RU2277476C2 (en) 2006-06-10

Similar Documents

Publication Publication Date Title
US7550185B2 (en) Port tube and closure composition, structure and assembly for a flowable material container
AU2002243476A1 (en) Port tube and closure composition, structure and assembly for a flowable material container
US6652942B2 (en) Assembly for a flowable material container
AU2002236711A1 (en) Laminate for a flowable material container
CA2540028C (en) High impact strength film and non-pvc containing container and pouch and overpouch
US20040122414A9 (en) Contoured tubing closure
JP4533885B2 (en) Peelable overpouch film
KR20040041154A (en) A steam-sterilizable multilayer film and containers made thereof
AU2005237132B2 (en) Port tube and closure composition, structure and assembly for a flowable material container
CA1205783A (en) Storage bag

Legal Events

Date Code Title Description
STCB Information on status: application discontinuation

Free format text: ABANDONED -- FAILURE TO RESPOND TO AN OFFICE ACTION