IE43534B1 - Thermoelastic polymers including block radial polymers to be used as pharmaceutical sealing and resealing materials - Google Patents
Thermoelastic polymers including block radial polymers to be used as pharmaceutical sealing and resealing materialsInfo
- Publication number
- IE43534B1 IE43534B1 IE1892/76A IE189276A IE43534B1 IE 43534 B1 IE43534 B1 IE 43534B1 IE 1892/76 A IE1892/76 A IE 1892/76A IE 189276 A IE189276 A IE 189276A IE 43534 B1 IE43534 B1 IE 43534B1
- Authority
- IE
- Ireland
- Prior art keywords
- weight
- copolymer
- composition
- styrene
- butadiene
- Prior art date
Links
- 239000000463 material Substances 0.000 title claims abstract description 35
- 238000007789 sealing Methods 0.000 title claims abstract description 7
- 229920000642 polymer Polymers 0.000 title abstract description 9
- 239000000203 mixture Substances 0.000 claims abstract description 57
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims abstract description 27
- 229920001400 block copolymer Polymers 0.000 claims abstract description 26
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 claims abstract description 22
- 229920001577 copolymer Polymers 0.000 claims abstract description 19
- 229920001169 thermoplastic Polymers 0.000 claims abstract description 19
- 239000004416 thermosoftening plastic Substances 0.000 claims abstract description 18
- 239000004721 Polyphenylene oxide Substances 0.000 claims abstract description 13
- 229920000570 polyether Polymers 0.000 claims abstract description 13
- 239000004709 Chlorinated polyethylene Substances 0.000 claims abstract description 12
- 229920000728 polyester Polymers 0.000 claims abstract description 12
- 229920006311 Urethane elastomer Polymers 0.000 claims abstract description 11
- 229920001971 elastomer Polymers 0.000 claims abstract description 8
- 229920000089 Cyclic olefin copolymer Polymers 0.000 claims abstract description 4
- 239000004952 Polyamide Substances 0.000 claims abstract description 4
- 239000011354 acetal resin Substances 0.000 claims abstract description 4
- 229920002647 polyamide Polymers 0.000 claims abstract description 4
- 229920000098 polyolefin Polymers 0.000 claims abstract description 4
- 229920006324 polyoxymethylene Polymers 0.000 claims abstract description 4
- 229920001897 terpolymer Polymers 0.000 claims abstract description 4
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 claims abstract description 3
- 239000000806 elastomer Substances 0.000 claims abstract description 3
- 229920000647 polyepoxide Polymers 0.000 claims abstract description 3
- MTAZNLWOLGHBHU-UHFFFAOYSA-N butadiene-styrene rubber Chemical compound C=CC=C.C=CC1=CC=CC=C1 MTAZNLWOLGHBHU-UHFFFAOYSA-N 0.000 claims description 16
- 239000004793 Polystyrene Substances 0.000 claims description 4
- 229920002223 polystyrene Polymers 0.000 claims description 4
- 239000004925 Acrylic resin Substances 0.000 claims description 3
- 229920000178 Acrylic resin Polymers 0.000 claims description 3
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 claims description 3
- 229920001519 homopolymer Polymers 0.000 claims description 3
- DHKHKXVYLBGOIT-UHFFFAOYSA-N 1,1-Diethoxyethane Chemical compound CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 claims description 2
- 239000003822 epoxy resin Substances 0.000 claims description 2
- 239000004431 polycarbonate resin Substances 0.000 claims description 2
- 229920005668 polycarbonate resin Polymers 0.000 claims description 2
- 239000004417 polycarbonate Substances 0.000 abstract description 2
- 229920000515 polycarbonate Polymers 0.000 abstract description 2
- 239000004593 Epoxy Substances 0.000 abstract 1
- 229920006397 acrylic thermoplastic Polymers 0.000 abstract 1
- 125000003700 epoxy group Chemical group 0.000 abstract 1
- 229920003229 poly(methyl methacrylate) Polymers 0.000 abstract 1
- ISXSCDLOGDJUNJ-UHFFFAOYSA-N tert-butyl prop-2-enoate Chemical compound CC(C)(C)OC(=O)C=C ISXSCDLOGDJUNJ-UHFFFAOYSA-N 0.000 abstract 1
- 229920003023 plastic Polymers 0.000 description 9
- 239000004033 plastic Substances 0.000 description 9
- 239000003963 antioxidant agent Substances 0.000 description 8
- 238000000605 extraction Methods 0.000 description 8
- 238000007906 compression Methods 0.000 description 7
- 230000006835 compression Effects 0.000 description 7
- 238000000034 method Methods 0.000 description 7
- 239000004615 ingredient Substances 0.000 description 6
- 239000000314 lubricant Substances 0.000 description 5
- 239000004014 plasticizer Substances 0.000 description 5
- 239000005060 rubber Substances 0.000 description 5
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 4
- 230000003078 antioxidant effect Effects 0.000 description 4
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 4
- 239000002480 mineral oil Substances 0.000 description 4
- 235000010446 mineral oil Nutrition 0.000 description 4
- 238000002156 mixing Methods 0.000 description 4
- 239000002738 chelating agent Substances 0.000 description 3
- 239000000945 filler Substances 0.000 description 3
- 239000012530 fluid Substances 0.000 description 3
- 235000013872 montan acid ester Nutrition 0.000 description 3
- NFHFRUOZVGFOOS-UHFFFAOYSA-N palladium;triphenylphosphane Chemical compound [Pd].C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 NFHFRUOZVGFOOS-UHFFFAOYSA-N 0.000 description 3
- 238000007911 parenteral administration Methods 0.000 description 3
- 238000001125 extrusion Methods 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- 238000002347 injection Methods 0.000 description 2
- 239000007924 injection Substances 0.000 description 2
- 125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 229920013623 Solprene Polymers 0.000 description 1
- BGYHLZZASRKEJE-UHFFFAOYSA-N [3-[3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoyloxy]-2,2-bis[3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoyloxymethyl]propyl] 3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoate Chemical compound CC(C)(C)C1=C(O)C(C(C)(C)C)=CC(CCC(=O)OCC(COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)(COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)=C1 BGYHLZZASRKEJE-UHFFFAOYSA-N 0.000 description 1
- 210000001124 body fluid Anatomy 0.000 description 1
- 239000010839 body fluid Substances 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 150000002118 epoxides Chemical class 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 239000012634 fragment Substances 0.000 description 1
- 125000004464 hydroxyphenyl group Chemical group 0.000 description 1
- 238000007373 indentation Methods 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- SSDSCDGVMJFTEQ-UHFFFAOYSA-N octadecyl 3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)CCC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 SSDSCDGVMJFTEQ-UHFFFAOYSA-N 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- -1 polyethylene Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 230000002787 reinforcement Effects 0.000 description 1
- 238000010074 rubber mixing Methods 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 229920006132 styrene block copolymer Polymers 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 239000012815 thermoplastic material Substances 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 238000001721 transfer moulding Methods 0.000 description 1
- 238000004073 vulcanization Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L53/00—Compositions 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
- C08L53/02—Compositions 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M39/00—Tubes, tube connectors, tube couplings, valves, access sites or the like, specially adapted for medical use
- A61M39/02—Access sites
- A61M39/04—Access sites having pierceable self-sealing members
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L101/00—Compositions of unspecified macromolecular compounds
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L57/00—Compositions of unspecified polymers obtained by reactions only involving carbon-to-carbon unsaturated bonds
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M2205/00—General characteristics of the apparatus
- A61M2205/19—Constructional features of carpules, syringes or blisters
- A61M2205/192—Avoiding coring, e.g. preventing formation of particles during puncture
- A61M2205/197—Avoiding coring, e.g. preventing formation of particles during puncture by the seal material
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Polymers & Plastics (AREA)
- Medicinal Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Heart & Thoracic Surgery (AREA)
- Biomedical Technology (AREA)
- Anesthesiology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Life Sciences & Earth Sciences (AREA)
- Hematology (AREA)
- Animal Behavior & Ethology (AREA)
- Engineering & Computer Science (AREA)
- Pulmonology (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Materials For Medical Uses (AREA)
- Graft Or Block Polymers (AREA)
- Medical Preparation Storing Or Oral Administration Devices (AREA)
Abstract
1517099 Elastic polymer compositions ABBOTT LABORATORIES 25 Aug 1976 [26 Aug 1975] 35418/76 Headings C3B C3M and C3R Copolymer mixtures having elastic properties comprise (1) 10-90% radial block copolymer of 60-85% butadiene and 40-15% styrene having an average molecular weight of at least 150,000 and (2) 90-10% of a polymeric material selected from elastomeric polyolefins, olefin copolymers and terpolymers, vinyl acetate copolymers, polyether and polyester elastomers, acrylics, thermoplastic epoxies, styrene polymers, polycarbonates, acetal resins, polyamides, vinyl chloride polymers, chlorinated polyethylene and mixtures thereof. Exemplified polymeric materials are chlorinated polyethylene and mixtures thereof with polyether and polyester urethane elastomers. The compositions may be moulded into pharmaceutical sealing components, container closures, syringe plunger sealing rings and syringe bulbs.
Description
This invention relates to thermoplastic copolymer compositions which are useful in molding rubber-like materials for contact with body fluids. More particularly, it relates to a thermoplastic composition which comprises a radial block copolymer of butadiene and styrene which has blended with it one or more additional polymeric materials so as to form a rubberlike composition having a high degree of elasticity and resealability. Such a material is useful for puncturable, reseal units for parenteral administration equipment as well as for containers for materials intended for administration to the body. They may also be used in other rubber applications such as syringe bulbs.
Recently, radial block polymers of the butadienestyrene type have become of particular interest in that they display high tensile strength without vulcanization or filler reinforcement. In U.S. Patents Nos. 3,281,383 and 3,078,254» a process of making such radial block copolymers is described. Further, particular blends of butadiene-styrene block copolymers are described in U.S. Patent Nos. 3,646,101. In U.S. Patent No. 3,562,355, a mechanical blend of a butadiene-styrene copolymer in admixture with a polyester urethane is disclosed. The prior art nowhere describes radial block copolymers of the butadiene-styrene type containing particular ranges of butadiene and styrene which - 3 when admixed with specific other polymeric materials will form a plastics material composition having a sufficient elasticity and resealability so that the compositions are readily adaptable For use in formul5 ating plastic closure materials having reseal properties for contact with fluids to be administered to the body. Moreover, the prior art does not describe a plastic composition which is suitable for use in the medical plastics field and which will have sufficient low alkaline extraction values to ensure that ingredients in the composition are not extracted in with the fluids to be administered after contact with the closure material.
The present invention seeks to provide s novel admixture of radial block copolymers of the butadienestyrene type with certain other polymeric materials.
It further seeks to provide a thermoplastic, polymer composition of the radial block copolymer type which has a high degree of elasticity and resealability so that it can be employed as resealable injection sites in parenteral administration equipment, to provide a novel radial block copolymer mixture which can be readily molded, extruded and otherwise processed by customary processes, a thermoplastic polymer compos25 ition which is compatible and can be sealed or otherwise connected to other types of plastic materials in a parenteral administration set, a novel thermoplastic composition which is compatible with the usual plasticizers, fillers, chelators and lubricants, which are necessary in the fabrication of plastics materials.
According to the present invention there is provided a thermoplastic copolymer composition having 53534 - 4 elastic properties which consists essentially of (a) from 10$ to 90% by weight of a butadiene-styrene radial block copolymer having a butadiene content of from 60% to 85% by weight and a styrene content of from 15% to 40% by weight and an average molecular weight of 150,000 to 300,000 (b) from 90% to 10% by weight of a polymeric material which is an elastomeric polyolefin, an olefin copolymer or terpolymer, a vinyl acetate copolymer, a polyether or polyester urethane elastomer, an acrylic resin, a thermoplastic epoxide resin, polystyrene or a styrene copolymer other than an impact resistant styrene copolymer, a polycarbonate resin, an acetal resin, a polyamide, a vi.nylchloridc homopolymer or copolymer or a chlorin15 ated polyethylene, or a mixture of such materials.
In one preferred composition, the radial block copolymer may have a butadiene content of substantially 70$ by weight and a styrene content of 30% by weight and in another preferred composition the butadiene-styrene copolymer may have a butadiene content of substantially 60% by weight and in another preferred composition the butadiene-styrene copolymer may have a butadiene content of substantially 60% by weight and a styrene content of substantially 40% by weight. These copoly25 mers are preferably individually admixed with a polyether or polyester urethane elastomer or a mixture of chlorinated polyethylene and a polyether or polyester urethane elastomer in the proportion of 25 to 75% by weight of copolymer to 75 to 25$ by weight of elast30 outer or mixture of chlorinated polyethylene and elastomer.
In the following Examples, certain polymers, plasvicizers, chelators, lubricants and antioxidants 34 - 5 are referred to as components of the compositions of this invention. All of the materials are readily available on the commercial market and a brief summary of them follows: Produc t Polymers Trade Name Source Radial block copolymer (70:30 butadienestyrene) Solprene"411 Phillips Petroleum Co.
Radial block copolymer (6θ:4θ butadienestyrene ) Solprene11 414 Phillips Petroleum Co.
Chlorinated polyethylene CPE-3023 Dow Chemical Co.
Polyether urethane umer elastRoylar E-85 Uniroyal Chemical Co., Division of Uniroyal, Inc.
Plasticizer Mineral Oil U.S.P. grade Any available Lubeleant Montanic acid ester Wax OP American Hoechst Corp.
Antioxidants 0ctadeeyl-3-(3',5'-ditertbutyl-4Lhydroxyphenyl)propionate Irganox 1076 Ciba-Geigy 53534 - 6 Product Trade Name Source Antioxidants Tetrakis [methylene-313 *,5'-di-t-butylhydroxyphenyl)-propionate] methane Irganox 1010 Ciba-Geigy Corp.
Of the above the word Solprene11 is a Registered Trade Mark.
The invention is illustrated by the following 10 Examples.
Example 1.
Ingredients Formula by Parts $ Comp 15 Butadiene- styrene radial block copolymer (70:30) 100.0 70.30 Chlorinated polyethylene 41.0 28.82 Mineral oil 1.0 0.7 20 Antioxidant (octadecyl 3-( 3 ',5 '-ditert-butyl-4 hydroxyphenyl) propionate) 0.25 0.18 142 .45 100.00 Formulations were prepared from the above ingredients by mixing the formulation on a basis of 300 grams of butadiene-styrene radial block copolymer. The mater43S34 - 7 ials were fused on a standard two-roller mill at 300°325°F. and milled until a homogeneous blend was obtained. Pharmaceutical closures of the reseal type were made from ground portions of the roller milled sheet by transfer molding. Test results obtained on these materials are reported as follows: Properties Shore A hardness Reseal after piercing (lbs :.) 71 24 10 Coring None 100% Modulus (psi) 300 Ultimate tensile (psi) 2690 % Elongation 690 Compression set (%, 250°F. -2 hrs.) 102 IS Nephelos extraction 44 % Elongation 690 Example II. 20 ingredients Formula by Parts % Comp. Butadiene-styrene radial block copolymer (60:40) 100.0 70.3 Chlorinated polyethylene 41.0 28.82 Mineral oil 1.0 0.7 25 Antioxidant (octadecyl 3(3s ,5 -di.tert-butyl-4'hydroxyphenyl)propionate) 0.25 0.18 142 .25 100.00 - 3 10 The materials were prepared in the same manner as described in Example I and the properties found are listed as follows: Properties Shore A11 hardness Reseal after piercing (lbs.) Coring 100% Modulus (psi) Ultimate tensile (psi) % Elongation Compression set (%, 25O°F.-2 hrs.) Nephelos extraction % Elongation Example III.
Formula by Ingredients Parts Butadiene-styrene radial block-copolymer (70:30) 40.0 Chlorinated polyethylene 25.0 Polyether urethane elastomer 35.0 Lubricant (montanic acid ester) 0.25 Antioxidant (tetrakis [methylene-3(3',5'-di-tbutyl-4'-hydroxyphenyl )propionate]methane) 0.25 100.50 None 475 3350 650 121 650 % Comp. 39.80 24.88 34.82 0.25 0.25 100.00 The materials were prepared in the same manner as described in Example I and the properties found are listed as follows: 3 S 3 4 Properties Shore A hardness 69 Reseal after piercing (lbs. ) 31 Coring None 100% Modulus (psi) 360 Ultimate tensile (psi) 2970 Compression set (%, 250°F.-2 hrs.) 9? Nephelos extraction 23 % Elongation 590 Example IV. Ingredients Formula by Parts % Comp. Butadiene-styrene radial block copolymer (60:40) 40.0 39.8 Chlorinated polyethylene 25.0 24.88 Polyester urethane elastomer 35.0 34.82 Lubricant (montanic acid ester) 0.25 0.25 Antioxidant (tetrakis [methylene-3(31,5'-di-t- butyl-4 '-hydroxyphenyl )propionatejmethane) 0.25 0.25 100.50 100.00 The materials were prepared as described in Example 1 and the properties found are indicated as follows: Properties Shore A hardness Reseal after piercing (lbs.) 32 Coring None 100% Modulus (psi) 400 Ultimate tensile (psi) 2800 Compression set (%, 250°F.-2 hrs.) 94 Nephelos extraction 23 % Elongation 600 An explanation of the various tests used in the preceding Examples is as follows: (1) The 100% Modulus, Ultimate Tensile and % Elongation were obtained using ASTM Test Method: D-412-66 using a Type C die and an Instron Tensile Tester, (the word Instron is a Registered Trade Mark) (a) 100% Modulus is the force required to elongate the dumbbell-shaped sample 100% using a one-inch bench mark for reference. (b) Ultimate Tensile is the force per cross sectional area required to pull the sample apart. (c) % Elongation is the elongation of the sample at break. A one-inch bench mark is placed on the sampl before elongation. Then the distance between the marks at break minus one inch multiplied by 100 gives the per centage elongation. (2) Compression Set - the lower the figure, the better rubber replacement is obtained. The value of the compression set number indicates how much permanent deformation occurred after the sample was compressed. 3 5 3 j - 11 (3) Nephelos Extraction - this is an alkaline extraction, pH il. A low value indicates a clean product. (4) Reseal - this is an internally devised test which shows how much air pressure is necessary to break the seal of the diaphragm after piercing with a 20gauge needle five times. A high value indicates a very good reseal. (5) Shore A Hardness - also referred to as Shore A Durometer (ASTM-D-2240), is a procedure for determining the indentation hardness of materials. This method is based on a specified indentor forced into the material under specified conditions. (6) Coring - the determination of the resistance to cutting of a rubber-like material when repeatedly pierced by a new sharp hypodermic needle. This test usually measures the particulate fragments generated by such piercing.
In the foregoing Examples, specific thermoplastic materials were indicated as being incorporated as the additional polymeric materials. Other copolymers may be utilized to impart an elastomeric effect to the radial block copolymer composed of the butadiene styrene moieties so long as such copolymers will impart desired properties such as hot strength and resistance to cold flow, are compatible at working levels, are useful in nontoxie applications and can be processed at 300Η-4θθϋ1·. in the composition. These are elastomeric polyolefins, olefin copolymers and terpolymers, vinyl acetate copolymers, polyether and polyester urethane elastomers, acrylic resins, thermoplastic epoxides, polystyrene and styrene copolymers other than impact resistant polystyrenes, polycarbonates, acetal resins, polyamides and vinylchloride homopolymers and copolymers. - 12 Certain proportions of the radial block copolymers and polymeric materials are utilized in the Examples.
The proportions of radial block copolymer which can be effectively employed is from 25$ to 75$ by weight of the total weight of the composition and the polymeric material can be present in an amount of from 75$ to 25$ by weight of the total weight of the composition. These amounts are suitable when a radial block copolymer of butadiene and styrene is employed with chlorinated poly10 ethylene and a polyether or polyester urethane elastomer alone. When mixtures of the polymeric materials and the radial block copolymer are used, the preferred amounts may range from 75$ to 40$ by weight of such mixture to from 25$ to 60$ by weight of the radial block copoly15 mer.
Plasticizers may be incorporated into the foregoing compositions in varying proportions. These plasticizers are those authorised for use by the U.S. Food and Drug Administration. The preferred plasticizers are U.S.P. grade mineral oil and monomeric epoxidized esters in proportions of less than 30$ by weight. Chelators, lubricants, antioxidants, pigments and fillers may be incorporated into these compositions in required proportions.
As indicated by the Examples the compositions may be mixed or blended by conventional plastics materials or rubber mixing methods. For example, mixing may be done by simple tumbling, intensive mixers, open mill mixing, Banbury mixing or by extrusion and pelleting or dicing. The novel rubber-like compositions of this invention may be compression, transfer, injection or blow and extrusion molded according to standard plastics articles forming techniques. The resulting product - 13 may be of various shapes and configurations such as a pharmaceutical sealing component including a puncturable reseal device, a container closure, a syringe sealing ring or other rubber products such as syringe bulbs.
It will thus be seen that the present invention provides a novel rubber-like composition which by reason of its physical characteristics can be utilized as a pharmaceutical rubber composition in components for administering fluids to the body. The composition has a high degree of elasticity and resealability yet can be processed by various plastic and rubber fabricating techniques. Most importantly, the compositions have .a very low extraction value which makes them especially suitable for use in conjunction with parenteral. solutions.
Claims (9)
1. A thermoplastic copolymer composition having elastic properties which consists essentially of (a) from 10% to 90% by weight of a butadiene-styrene 5 radial block copolymer having a butadiene content of from 60% to 85% by weight and a styrene content of from 15% to 40% by weight and having an average molecular weight of 150,000 to 300,000 and (b) from 90% to 10% by weight of a polymeric material which 10 is an elastomeric polyolefin, an olefin copolymer or terpolymer, a vinyl acetate copolymer, a polyether or polyester urethane elastomer, an acrylic resin, a thermoplastic epoxide resin, polystyrene or a styrene copolymer other than an impact resistant 15 styrene copolymer, a polycarbonate resin, an acetal resin, a polyamide, a vinylchloride homopolymer or copolymer or a chlorinated polyethylene, or a mixture of such materials.
2. A thermoplastic composition as claimed in claim 1 20 wherein said radial block copolymer has a butadiene styrene content of substantially 70% by weight of butadiene and 30% by weight of styrene.
3. A thermoplastic copolymer composition as claimed in claim 1 wherein said radial block copolymer has a 25 butadiene-styrene content of substantially 60% by weight of butadiene and 4θ% by weight of styrene.
4. A thermoplastic copolymer composition as claimed in any of claims 1 to 3 wherein said polymeric material (b) is a polyether or polyester urethane 30 elastomer. - 15
5. A thermoplastic copolymer composition as claimed in any of claims 1 to 3 wherein said polymeric material (b) is a chlorinated polyethylene or polyether or polyester urethane elastomer present in a proportion of 75% to 25% by weight of said composition and said radial block copolymer is present in an amount of 25% to 75% by weight of said composition.
6. A thermoplastic copolymer composition as claimed in any of claims 1 to 3 wherein said polymeric material (b) consists of a mixture of chlorinated polyethylene and a polyether urethane elastomer and said radial block copolymer is present in a proportion of 25% to 60% by weight of the composition and said mixture of polymeric materials is present, i.n a portion of 75% to 40% by weight of the composition.
7. A thermoplastic copolymer composition as claimed in any of claims 1 to 6 which has been molded to form a pharmaceutical sealing component.
8.S. A thermoplastic copolymer composition according to claim 7 in the form of a puncturable reseal device, a container closure, a syringe plunger sealing ring or a rubber-like syringe, bulb.
9. A thermoplastic copolymer composition as claimed in claim 1 and substantially as hereinbefore described with reference to any one of the Examples.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US60798175A | 1975-08-26 | 1975-08-26 |
Publications (2)
Publication Number | Publication Date |
---|---|
IE43534L IE43534L (en) | 1977-02-26 |
IE43534B1 true IE43534B1 (en) | 1981-03-25 |
Family
ID=24434527
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
IE1892/76A IE43534B1 (en) | 1975-08-26 | 1976-08-25 | Thermoelastic polymers including block radial polymers to be used as pharmaceutical sealing and resealing materials |
Country Status (9)
Country | Link |
---|---|
JP (1) | JPS5227448A (en) |
AU (1) | AU1617776A (en) |
BR (1) | BR7605486A (en) |
DE (1) | DE2638023A1 (en) |
FR (1) | FR2323738A1 (en) |
GB (1) | GB1517099A (en) |
IE (1) | IE43534B1 (en) |
SE (1) | SE7609335L (en) |
ZA (1) | ZA764161B (en) |
Families Citing this family (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB1552266A (en) * | 1976-03-27 | 1979-09-12 | Bayer Ag | Thermoplastic rubber |
CA1110374A (en) * | 1977-04-22 | 1981-10-06 | William P. Gergen | Compositions containing hydrogenated block copolymers and engineering thermoplastic resins |
US4126600A (en) * | 1977-05-05 | 1978-11-21 | Shell Oil Company | Multicomponent nitrile resin-block copolymer-polymer blends |
CA1098237A (en) * | 1977-05-05 | 1981-03-24 | William P. Gergen | Compositions containing hyrogenated block copolymers and engineering thermoplastic resins |
JPS5739446Y2 (en) * | 1978-03-30 | 1982-08-31 | ||
FR2444064A1 (en) * | 1978-12-15 | 1980-07-11 | Sodip Sa | MIXTURE OF VINYL CHLORIDE POLYMER AND POLYETHERURETHANE WITH A TERTIARY AND / OR AMMONIUM AMINE GROUP, IN PARTICULAR FOR A CONFORMED OBJECT FOR MEDICAL USE |
US4301255A (en) * | 1979-07-05 | 1981-11-17 | Permacel | Novel alloy compositions and products |
FR2465765A1 (en) * | 1979-09-18 | 1981-03-27 | Rhone Poulenc Ind | Polyamide compsn. contg. thermoplastic elastomer - pref. butadiene! styrene! block copolymer to increase resilience and reduce modulus of elasticity |
JPS5857455A (en) * | 1981-09-30 | 1983-04-05 | Dainippon Ink & Chem Inc | Thermoplastic elastomer composition |
JPS58165864A (en) * | 1982-03-29 | 1983-09-30 | テルモ株式会社 | Medical instrument |
ATE67038T1 (en) * | 1982-06-15 | 1991-09-15 | Raychem Corp | SONAR SYSTEM CONTAINING HIGH DAMPING POLYMER COMPOUNDS. |
JPS59223744A (en) * | 1983-02-01 | 1984-12-15 | Denki Kagaku Kogyo Kk | Thermoplastic elastomer composition |
DE3620690C2 (en) * | 1986-06-20 | 1994-02-17 | Ds Chemie Gmbh | Sealing element |
US5028659A (en) * | 1989-06-05 | 1991-07-02 | Eastman Kodak Company | Impact resistant polymer blends |
US5496862A (en) | 1993-05-05 | 1996-03-05 | Supreme Corq | Molded styrene block copolymer closure for a wine container |
-
1976
- 1976-07-13 ZA ZA764161A patent/ZA764161B/en unknown
- 1976-07-23 AU AU16177/76A patent/AU1617776A/en not_active Expired
- 1976-08-20 BR BR7605486A patent/BR7605486A/en unknown
- 1976-08-23 SE SE7609335A patent/SE7609335L/en unknown
- 1976-08-24 DE DE19762638023 patent/DE2638023A1/en active Pending
- 1976-08-25 FR FR7625749A patent/FR2323738A1/en not_active Withdrawn
- 1976-08-25 IE IE1892/76A patent/IE43534B1/en unknown
- 1976-08-25 GB GB35418/76A patent/GB1517099A/en not_active Expired
- 1976-08-26 JP JP51101206A patent/JPS5227448A/en active Pending
Also Published As
Publication number | Publication date |
---|---|
DE2638023A1 (en) | 1977-03-10 |
IE43534L (en) | 1977-02-26 |
JPS5227448A (en) | 1977-03-01 |
FR2323738A1 (en) | 1977-04-08 |
AU1617776A (en) | 1978-01-26 |
BR7605486A (en) | 1977-08-16 |
ZA764161B (en) | 1977-06-29 |
GB1517099A (en) | 1978-07-12 |
SE7609335L (en) | 1977-02-27 |
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