IE52850B1 - Elastomeric bladders for medical infusers - Google Patents
Elastomeric bladders for medical infusersInfo
- Publication number
- IE52850B1 IE52850B1 IE370/82A IE37082A IE52850B1 IE 52850 B1 IE52850 B1 IE 52850B1 IE 370/82 A IE370/82 A IE 370/82A IE 37082 A IE37082 A IE 37082A IE 52850 B1 IE52850 B1 IE 52850B1
- Authority
- IE
- Ireland
- Prior art keywords
- antioxidant
- silicon dioxide
- phr
- bladder
- elastomeric bladder
- Prior art date
Links
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims abstract description 61
- 239000003963 antioxidant agent Substances 0.000 claims abstract description 47
- 230000003078 antioxidant effect Effects 0.000 claims abstract description 43
- 239000000377 silicon dioxide Substances 0.000 claims abstract description 30
- 235000012239 silicon dioxide Nutrition 0.000 claims abstract description 27
- 229920003051 synthetic elastomer Polymers 0.000 claims abstract description 20
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 19
- 239000000203 mixture Substances 0.000 claims abstract description 19
- 239000006229 carbon black Substances 0.000 claims abstract description 17
- 239000002904 solvent Substances 0.000 claims abstract description 11
- 231100000252 nontoxic Toxicity 0.000 claims abstract description 8
- 230000003000 nontoxic effect Effects 0.000 claims abstract description 8
- 208000034713 Spontaneous Rupture Diseases 0.000 claims abstract description 5
- 239000007857 degradation product Substances 0.000 claims abstract description 5
- 239000008240 homogeneous mixture Substances 0.000 claims abstract description 3
- 239000006193 liquid solution Substances 0.000 claims abstract description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 claims description 18
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims description 15
- 238000000034 method Methods 0.000 claims description 13
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 claims description 7
- XMNIXWIUMCBBBL-UHFFFAOYSA-N 2-(2-phenylpropan-2-ylperoxy)propan-2-ylbenzene Chemical compound C=1C=CC=CC=1C(C)(C)OOC(C)(C)C1=CC=CC=C1 XMNIXWIUMCBBBL-UHFFFAOYSA-N 0.000 claims description 4
- 239000007983 Tris buffer Substances 0.000 claims description 4
- 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 claims description 4
- 150000008442 polyphenolic compounds Chemical class 0.000 claims description 4
- 235000013824 polyphenols Nutrition 0.000 claims description 4
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 claims description 3
- 229910052799 carbon Inorganic materials 0.000 claims description 3
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 claims description 3
- 238000010525 oxidative degradation reaction Methods 0.000 claims description 3
- -1 1 -hydroxyphenyl Chemical group 0.000 claims description 2
- 238000002156 mixing Methods 0.000 claims description 2
- ZAAQJFLUOUQAOG-UHFFFAOYSA-N 4-benzyl-2,6-ditert-butylphenol Chemical compound CC(C)(C)C1=C(O)C(C(C)(C)C)=CC(CC=2C=CC=CC=2)=C1 ZAAQJFLUOUQAOG-UHFFFAOYSA-N 0.000 claims 1
- 125000006289 hydroxybenzyl group Chemical group 0.000 claims 1
- 238000000638 solvent extraction Methods 0.000 abstract 1
- 238000000605 extraction Methods 0.000 description 7
- 239000007788 liquid Substances 0.000 description 7
- 239000000243 solution Substances 0.000 description 6
- 239000012530 fluid Substances 0.000 description 4
- 229920001195 polyisoprene Polymers 0.000 description 4
- 238000012360 testing method Methods 0.000 description 4
- 238000004073 vulcanization Methods 0.000 description 4
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 238000005213 imbibition Methods 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- 238000004438 BET method Methods 0.000 description 2
- 238000009792 diffusion process Methods 0.000 description 2
- 238000003801 milling Methods 0.000 description 2
- 238000012546 transfer Methods 0.000 description 2
- VXEGSRKPIUDPQT-UHFFFAOYSA-N 4-[4-(4-methoxyphenyl)piperazin-1-yl]aniline Chemical compound C1=CC(OC)=CC=C1N1CCN(C=2C=CC(N)=CC=2)CC1 VXEGSRKPIUDPQT-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical group CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 1
- 229920004940 NATSYN® Polymers 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 238000000944 Soxhlet extraction Methods 0.000 description 1
- 206010046530 Urinary bladder rupture Diseases 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 230000033228 biological regulation Effects 0.000 description 1
- 238000003490 calendering Methods 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- 230000002939 deleterious effect Effects 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 230000004927 fusion Effects 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 238000001802 infusion Methods 0.000 description 1
- 230000005764 inhibitory process Effects 0.000 description 1
- 238000001746 injection moulding Methods 0.000 description 1
- 230000002045 lasting effect Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- 239000005049 silicon tetrachloride Substances 0.000 description 1
- 230000008961 swelling Effects 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 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
- C08L9/00—Compositions of homopolymers or copolymers of conjugated diene hydrocarbons
-
- 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
- A61M5/00—Devices for bringing media into the body in a subcutaneous, intra-vascular or intramuscular way; Accessories therefor, e.g. filling or cleaning devices, arm-rests
- A61M5/14—Infusion devices, e.g. infusing by gravity; Blood infusion; Accessories therefor
- A61M5/142—Pressure infusion, e.g. using pumps
- A61M5/145—Pressure infusion, e.g. using pumps using pressurised reservoirs, e.g. pressurised by means of pistons
- A61M5/148—Pressure infusion, e.g. using pumps using pressurised reservoirs, e.g. pressurised by means of pistons flexible, e.g. independent bags
- A61M5/152—Pressure infusion, e.g. using pumps using pressurised reservoirs, e.g. pressurised by means of pistons flexible, e.g. independent bags pressurised by contraction of elastic reservoirs
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Biomedical Technology (AREA)
- Heart & Thoracic Surgery (AREA)
- Hematology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Anesthesiology (AREA)
- Vascular Medicine (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Medical Preparation Storing Or Oral Administration Devices (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Materials For Medical Uses (AREA)
- Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)
- Infusion, Injection, And Reservoir Apparatuses (AREA)
Abstract
Elastomeric bladders having improved resistance to spontaneous rupture when inflated are made by vulcanizing a homogeneous mixture of synthetic polyisoprene having 90% to 98% cis-1,4 linkages, finely divided silicon dioxide or carbon black, and vulcanizing agent while simultaneously forming the mixture into hollow tubular bodies. After being formed the bodies are solvent extracted to remove unreacted vulcanizing agent and the degradation products of the vulcanizing agent. Following the solvent extraction a nontoxic, nonleachable antioxidant is imbibed into the bodies by contacting the bodies with a liquid solution of the antioxidant.
Description
This invention relates to synthetic polyisoprene bladders for medical infusers which have improved resistance to spontaneous rupture.
Medical devices that infuse liquids into patients 5 are called infusers. One type of infuser uses an elastomeric bladder as its power source. Such infusers and bladders are described in U.S. Patent Specifications Nos. 3,993,069 and 4,201,207. These infusers consist of a housing, an elastomeric bladder contained within the housing that is inflated with the liquid to be infused, and a conduit that leads from the bladder to the infusion site. The fate at which the liquid is infused from the infuser depends upon the pressure exerted on the liquid by the bladder, the viscosity of the liquid, and the flow restriction characteristics of the conduit. The above cited specifications describe bladders that are capable of maintaining the pressure on the liquid substantially constant over discharge of a large proportion of the liquid. The bladders described in these specifications are made from vulcanized synthetic polyisoprene that has a low frequency hysteresis less than about 10% and a stress relaxation less than about 10%. Such hysteresis and stress relaxation characteristics were considered as key factors in realizing substantially constant pressure performance.
In making large numbers of such bladders from synthetic polyisoprene it was found that a small but significant number of them ruptured when inflated particularly after prolonged storage in an inflated state. Even though only a small portion of the bladders so ruptured it was desirable to decrease the incidence of rupture in order to provide a greater margin of safety against rupture in the marketplace. The above specifications say nothing about reducing the incidence / of bladder rupture.
A principal object of the present invention is to provide synthetic polyisoprene bladders that have a reduced incidence of rupture and acceptable pressure constancy performance.
One aspect of the invention is an elastomeric bladder for use in a medical infuser comprising a tubular body formed of a vulcanized homogeneous mixture of synthetic polyisoprene having 90% to 98% cis-1, linkages said bladder having improved resistance to rupture when inflated and being characterized by containing particulate silicon dioxide or particulate carbon black having a nominal average diameter in the -5 -3 range of about 1 x 10 to about 5 x 10 mm; and a nontoxic, substantially nonleachable antioxidant diffused throughout the mixture, the amounts of silicon dioxide or carbon black and antioxidant being sufficient to make the half-life of a population of the bladders at 4O°C at least about ten times longer than the halflife of a comparable population of bladders made from said vulcanized synthetic polyisoprene but without the silicon dioxide or carbon black and the antioxidant.
Another aspect of the invention is a process for making an elastomeric bladder for use in a medical infuser having improved resistance to rupture when inflated comprising mixing homogeneously a synthetic polyisoprene having about 90% to about 98% cis-1,4 linkages, a sufficient amount of particulate silicon dioxide or particulate carbon black which have a nominal average diameter in the range of about 1 x 10 to about _3 x 10 mm to substantially inhibit spontaneous rupture of the bladder due to stress in the bladder wall caused by inflation of the bladder and an amount of vulcanizing agent sufficient to vulcanize the mixture and vulcanizing said mixture said process being characterized by subjecting the mixture to vulcanizing conditions while; a) forming the mixture into a tubular body; b) solvent extracting unreacted vulcanizing agent and the degradation products of the vulcanizing agent from the body; and - 4 52850 c) diffusing a nontoxic, substantially nonleachable antioxidant into the body by contacting the body with a liquid solution of the antioxidant, the amount of antioxidant diffused into the body being sufficient to substantially inhibit oxidative degradation of the body.
As used herein the designation phr means parts per hundred parts of synthetic polyisoprene, and parts are by weight. t The synthetic polyisoprene that is used to make the bladders has about 90% to 98% of its monomeric units joined in cis-1,4 orientation. It is preferably of the type made using Ziegler catalysts which is characterized by having about 96% to about 98% cis-1,4 linkages. This polyisoprene is mixed homogeneously with particulate silicon dioxide or particulate carbon black or mixtures thereof which have the above indicated particle size.
Fumed silicon dioxide is preferred, such silicon dioxide is produced by the hydrolysis of silicon tetrachloride vapour in a flame of hydrogen and oxygen at temperatures above the fusion temperature of silica (ca 1710°C).
In this combustion process molten spheres of silica are formed that on cooling fuse with one another to form branched, three dimensional, chain-like aggregates. The final product typically has a surface area in the range of 2 about 150 to about 450 m /gram, preferably 200 + 20 m /gram, as measured by the BET method. Such fumed silicon dioxides are sold by Cabot Corporation, Boston, Mass, under the trade mark Cab-O-Sil. The carbon black will typically have a surface area in the range of about 50 to about 250 m /gram as measured by the BET method. The amount of silicon dioxide or carbon black that is mixed with the polyisoprene should be sufficient to substantially inhibit spontaneous rupture of the bladder due to the stresses that occur in the bladder walls when the bladder is inflated with medical fluid. About 3 to about 10 phr, preferably 3 to 7 phr, of the silicon dioxide or carbon black will normally be mixed with the synthetic polyisoprene. Lesser amounts will not give a significant increase in rupture resistance. More than 10 phr may be added, but such amounts do not produce correspondingly greater enhancement of rupture resistance and may affect the pressure constancy performance of the bladder adversely.
The polyisoprene-silicon dioxide/carbon black mixture is vulcanized to form carbon-to-carbon or monothio crosslinks at the 1 and 4 positions of the isoprene unit.
To achieve such vulcanization a vulcanizing agent is added to the mixture and the mixture is subjected to vulcanization conditions. Vulcanizing agents and procedures that may be used are disclosed in U.S. Patent Specification No. 4,201,207 - 6 52850 at column 2, line 54 to column 3, line 13 and in U.S. Patent Specification No. 3,993,069 at column 8, line 50 to column 10, line 25, which disclosures are incorporated herein by reference. Dicumyl peroxide added in amounts in the range of about 1 to 2 phr is a preferred vulcanizing agent. The vulcanization will typically be effected during the forming process that is used to make the tubular bodies from the mixture.
One such process involves calendering the polyisoprenesilicon dioxide/carbon black-vulcanizing agent mixture into a sheet and placing a disc-shaped segment of the sheet into a transfer mold that forms the sheet into hollow cylindrical tubes of the desired geometry.
Conventional injection molding techniques may also be used to form the body. The moulding temperature, pressure, and time are such as to achieve the desired vulcanization (crosslinking) of the polyisoprene. The geometry of the tubular bodies is the same as that disclosed in U.S. Patent Specification No. 3,993,069 at column 4, lines 26 to 41, which disclosure is incorporated herein by reference.
After the mixture is formed into tubular bodies, the bodies are extracted with a solvent that removes substantially all unreacted vulcanizing agent and the degradation products of the vulcanizing agent from the body. The solvent should have no lasting deleterious effects on the body and should not leave a toxic residue in or on the body. The particular solvent used and the extraction time and temperature will depend upon the vulcanizing agent that was used. The purpose of the extraction is to prevent contamination of the medical fluid that is ultimately charged to the bladder with the vulcanizing agent or its degradation products.
After the extraction, the antioxidant is imbibed into the bodies by placing them into contact with a solution of the antioxidant. The antioxidant enters the bodies, which are usually swollen several fold with solvent, by diffusion. The amount of antioxidant imbibed into a body will, accordingly, depend upon the diffusion coefficient of the body with respect to the antioxidant, the concentration of the antioxidant in the solution, the solubility of the antioxidant in the body, the thickness of the body, the equilibrium swelling volume that is characteristic of the elastomeric-solvent combination and the conditions (time and temperature) under which the contact is made. Preferably the same pure solvent is used for the extraction and antioxidant imbibition. The amount of antioxidant imbibed into the body should be sufficient to inhibit oxidative degradation (and thus rupture) of the bladder, usually over a period of at least about one year. The quantity - 8 52850 required to achieve such inhibition will depend on the particular antioxidant that is used. In the case of the hindered phenol antioxidants described below, about 0.2 to about 2 phr, preferably about 1 phr, will usually be imbibed. Antioxidants that are nontoxic, such as those approved and under the provisions of Title 21 of the Code of Federal Regulations for use in plastics that are used in association with drugs or food,and which are substantially nonleachable by the medical fluid with which the bladder is to be inflated may be used. The term substantially nonleachable means that the antioxidant is less than 0.1% by weight soluble in the medical fluid. Nontoxic hindered polyphenol antioxidants, such as tetrakis (methylene ΙΟ’ ,5'-di-t-buty1-4'-hydroxyphenyl) propionate! methane and l,3,5-trimethyl-2,4,6-tris(3,5-di-t-butyl-4-4hydroxybenzyl) benzene, are preferred antioxidants for use in the invention. After the desired amount of antioxidant has diffused into the body, the body is taken from the solution and the solvent is removed from the body, such as o by drying at temperatures up to 50 C. At this stage, the bladder is ready for incorporation into the infuser.
The inclusion of the silicon dioxide or carbon black and the antioxidant in the bladder together substantially reduce the likelihood that the bladder will rupture spontaneously when it is inflated. The reduction (or increase in rupture resistance) may be quantified relative to synthetic polyisoprene bladders that do not contain silicon dioxide or carbon black and antioxidant by comparing the half-lives of populations of the respective bladders under the same inflation conditions. The half-life is the time period from inflation to rupture of 50% of the bladders in the population. A population of at least ten bladders is desired to ensure that the results are statistically significant. Such comparisons carried out at 40°C indicate that the half life of the invention bladders is at least 10 times, and typically more than 100 times, longer than the half-life of bladders that do not contain silicon dioxide or carbon black and antioxidant.
The following example illustrates one embodiment of the invention. This example is not intended to limit the invention and is offered only by way of examplification One hundred parts of synthetic polyisoprene (Natsyn (Trade Mark) 2200, 96% to 98% cis-1,4 linkages) were added to a Farrell Laboratory Mill ( 6 x 13 inch; 15.3 cm x 33.00 cm, rolls) at 130°F ± 10°F (54°C - 5°C) and the gap between rolls was adjusted to 0.08-0.09 inch; (0.2 - 0.225 cm). After about 3 minutes of milling, .0 phr fumed silicon dioxide (Cab-O-Sil M5, 200 — 25 m2/ gram surface area, 1.4 x 10 mm nominal average diameter were added to the mill over a 5 min period. One and one-half phr of dicumyl peroxide (Di Cup s (Trade Mark) were added to the polyisoprene-silicon dioxide mix in four equal portions. Milling was continued until at least 18 mins, had elapsed from the time the polyisoprene was added to the mill.
The above mixture was charged to a four cavity transfer mold maintained at 325° - 33O°F (162 - 165°C) and having 25,000 kg of clamping force. The mold cavities and mandrels were designed to make hollow cylindrical bladders 75.6 mm long with a 6.63 mm outer diameter and 5.16 mm inner diameter and having an integral circular flange at each end 1.587 mm wide and 12.7 mm in diameter.
The curing time was 20 min.
Extraction Bladders formed and vulcanized as above were placed vertically in the extraction pot of a Soxhlet extraction apparatus fitted to a 1000 ml flask. Enough ethyl acetate was added to fill the Soxhlet apparatus and have 250 ml of ethyl acetate in the flask. The flask was heated and extraction of the bladders with the ethyl acetate was carried out for four hours.
Imbibition of Antioxidant A 1.1% by weight solution of l,3,5-trimethyl-2,4,6tris (3,4-dl-t-butyl-4-hydroxybenzyl) benzene in ethyl acetate 2 8 5θ was placed in a flask. Freshly extracted bladders were placed into the solution and kept there at ambient temperature for four hours. Previous tests had shown that the relationship between the wt.% of this antioxidant imbibed into the bladders was linear with 0.45% imbibed at a 1% concentration, and 0.68% imbibed at 1.5% concentration (four hours imbibition time). Accordingly about 0.5 phr antioxidant was imbibed into the bladders.
Half-life Tests Half-life tests were carried out on bladders prepared as above except that 1.2 phr of tetrakis (methylene 3(31,5'-di-t-butyl-4'-hydroxyphenyl) propionate}methane was imbibed into the bladders from an acetone/toluene solution instead of the above described antioxidant. A population of 24 of these bladders inflated with 60 ml water and kept in air at 40°C had a half-life of approximately 14 months. Similar tests on populations of synthetic polyisoprene bladders made in substantially the same manner but without silicon dioxide or antioxidant indicate such bladders have a half-life of about 1 to 2 days.
Modification of the above-described bladders that are obvious to those of ordinary skill in the arts related to the invention are intended to be within the scope of the following claims.
Claims (17)
1. An elastomeric bladder for use In a medical infuser comprising a tubular body formed of a vulcanized homogeneous mixture of synthetic polyisoprene having 90% to 98% cis-1,4 linkages said bladder having improved resistance to rupture when inflated and being characterized by containing particulate silicon dioxide or particulate carbon black having a nominal average diameter in the range of about -5 -3 1 x 10 to about 5 x 10 mm; and a nontoxic, substantially nonleachable antioxidant diffused throughout the mixture, the amounts of silicon dioxide or carbon black and antioxidant being sufficient to make the half-life of a population of the bladders at 40°C at least about ten times longer than the half-life of a comparable population of bladders made from said vulcanized synthetic polyisoprene but without the silicon dioxide or carbon black and the antioxidant.
2. The elastomeric bladder of claim 1 further characterized in the particulate silicon dioxide is fumed silicon dioxide and is present in amounts of from 3 to 10 phr.
3. The elastomeric bladder of claim 1 or 2 further characterized by the synthetic polyisoprene having about 96% to 98% cis-1, 4 linkages.
4. The elastomeric bladder of claim 1, 2 or 3, further characterized by the vulcanized synthetic polyisoprene having carbon-to-carbon crosslinks.
5. The elastomeric bladder of claims 1, 2, 3 or 4 5 further characterized by containing from about 0.2 to about 2 phr of the nontoxic, substantially nonleachable antioxidant.
6. The elastomeric bladder of claims 1, 3, 4 or 5, being further characterized by containing about 3 to about 10 7 phr of fumed silicon dioxide having a surface area in the range of 150 to about 450 m /gram.
7. The elastomeric bladder of claim 6 being further characterized by the surface area being 200 + 20 m /gram.
8. The elastomeric bladder of claim. 1, 2, 3, 4, 5, 15 6 or 7, being further characterized by the antioxidant being a hindered polyphenol.
9. The elastomeric bladder of claim 8 being further characterized by the hindered polyphenol being tetrakis (methylene 3-(3 1 - 5', di-t-butyl-4’- hydroxyphenyl) 20 propionatql methane or 1, 3,5-trimethyl-2,4,6-tris (3,5-dit-butyl-4-hydroxyhenzyl) benzene.
10. The elastomeric bladder of claim 9 being further characterized by being vulcanized with about 1.5 phr dicumyl peroxide; and containing about 1 phr of 1,3, 25 5-trimethyl-2,4,6-tris (3,5-di-t-butyl-4-hydroxybenzyl) benzene. - 14 52850
11. A process for making an elastomeric bladder for use in a medical infuser having improved resistance to rupture when inflated comprising mixing homogeneously a synthetic polyisoprene having about 90% to about 98% cis-1,4 linkages, a sufficient amount of particulate silicon dioxide or particulate carbon black which have a _5 nominal average diameter in the range of about 1 x 10 mm to about 5 x 10 -3 mm to substantially inhibit spontaneous rupture of the bladder due to stress in the bladder wall caused by inflaticn of the bladder and an amount of vulcanizing agent sufficient to vulcanize the mixture and vulcanizing said mixture^ said process being characterized by subjecting the mixture to vulcanizing conditions while a) forming the mixture into a tubular body; b) solvent extracting unreacted vulcanizing agent and the degradation products of the vulcanizing agent from the body; and o) diffusing a nontoxic, substantially nonleachable antioxidant into the body by contacting the body with a liquid solution of the antioxidant, the amount of antioxidant diffused into the body being sufficient to substantially inhibit oxidative degradation of the body.
12. The process of claim 11 being further characterised by said synthetic polyisoprene being mixed with fumed silicon dioxide.
13. The process of claim 12 being further characterized by the amount of fumed silicon dioxide being about 3 to about 10 phr, the antioxidant 5 being a hindered polyphenol, and the amount of antioxidant being about 0.2 to about 2 phr.
14. The process of Claim 13 being further characterised by the fumed silicon dioxide having a surface area of 200 + 20 m /gram, the amount of fumed 10 silicon dioxide being 5 phr, the vulcanizing agent being dicumyl peroxide, the amount of vulcanizing agent being 1.5 phr, the antioxidant being tetrakis jmethylene 3-(3',5',di-t-buty1-4 1 -hydroxyphenyl) propionate] methane or l,3,5-trimethyl-2-4,6-tris (3,5-di-t-butyl-415 hydroxy-benzyl) benzene, and the amount of antioxidant being about 0.2 to about 2 phr.
15. The process of Claim 14 being further characterised by antioxidant being l,3,5-trimethyl-2,4,6tris(3,5-di-t-buty-4-hydroxybenzyl) benzene, the amount 20 of antioxidant being 1 phr, the solvent being ethyl acetate, and the antioxidant being dissolved in ethyl acetate.
16. An elastomeric bladder as claimed in claim 1 and substantially as herein described.
17. A process as claimed in Claim 11 and 25 substantially as described in the specific embodiment hereinbefore set forth.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US23732581A | 1981-02-23 | 1981-02-23 |
Publications (2)
Publication Number | Publication Date |
---|---|
IE820370L IE820370L (en) | 1982-08-23 |
IE52850B1 true IE52850B1 (en) | 1988-03-30 |
Family
ID=22893262
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
IE370/82A IE52850B1 (en) | 1981-02-23 | 1982-02-22 | Elastomeric bladders for medical infusers |
Country Status (21)
Country | Link |
---|---|
JP (1) | JPS57156772A (en) |
AR (1) | AR228472A1 (en) |
AT (1) | AT386953B (en) |
AU (1) | AU548485B2 (en) |
BE (1) | BE892189A (en) |
BR (1) | BR8200915A (en) |
CA (1) | CA1213097A (en) |
CH (1) | CH658194A5 (en) |
DE (1) | DE3206377A1 (en) |
DK (1) | DK159051C (en) |
ES (1) | ES509733A0 (en) |
FR (1) | FR2502013B1 (en) |
GB (1) | GB2093473B (en) |
IE (1) | IE52850B1 (en) |
IL (1) | IL65081A (en) |
IT (1) | IT1191167B (en) |
MX (1) | MX163246B (en) |
NL (1) | NL189111C (en) |
NO (1) | NO154181C (en) |
SE (1) | SE452711B (en) |
ZA (1) | ZA82268B (en) |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4419096A (en) * | 1982-02-22 | 1983-12-06 | Alza Corporation | Elastomeric bladder assembly |
CA1241474A (en) * | 1983-01-10 | 1988-08-30 | Robert L. Buchanan | Method of making rubber connectors and other rubber parts for use in human infusion sets and products produced thereby and novel compositions |
WO1988000841A1 (en) * | 1986-08-08 | 1988-02-11 | Edward John Keogh | Expansible chamber drug infuser system |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB1195926A (en) * | 1968-05-08 | 1970-06-24 | Oliver Wallis Burke Jr | Silica Pigment Reinforced Hydrocarbon Rubber Compounded Stocks and Vulcanizates thereof and Processes for Producing the Same. |
IE34924B1 (en) * | 1970-02-26 | 1975-09-17 | Pirelli | Tear-resistant rubber-base cured composition to be used for heavy-duty articles |
US4201207A (en) * | 1973-03-26 | 1980-05-06 | Alza Corporation | Bladder for liquid dispenser |
US3993069A (en) * | 1973-03-26 | 1976-11-23 | Alza Corporation | Liquid delivery device bladder |
DE2822148C2 (en) * | 1978-05-20 | 1983-02-24 | Chemische Werke Hüls AG, 4370 Marl | Process for the production of a powdery, filler-containing rubber |
-
1982
- 1982-01-08 AU AU79406/82A patent/AU548485B2/en not_active Ceased
- 1982-01-08 GB GB8200523A patent/GB2093473B/en not_active Expired
- 1982-01-15 ZA ZA82268A patent/ZA82268B/en unknown
- 1982-01-21 NL NLAANVRAGE8200218,A patent/NL189111C/en not_active IP Right Cessation
- 1982-01-21 DK DK025582A patent/DK159051C/en not_active IP Right Cessation
- 1982-01-29 AR AR288296A patent/AR228472A1/en active
- 1982-02-10 AT AT0049982A patent/AT386953B/en not_active IP Right Cessation
- 1982-02-10 IT IT67153/82A patent/IT1191167B/en active
- 1982-02-18 ES ES509733A patent/ES509733A0/en active Granted
- 1982-02-18 SE SE8201009A patent/SE452711B/en not_active IP Right Cessation
- 1982-02-18 CH CH1027/82A patent/CH658194A5/en not_active IP Right Cessation
- 1982-02-18 BE BE0/207346A patent/BE892189A/en not_active IP Right Cessation
- 1982-02-19 BR BR8200915A patent/BR8200915A/en not_active IP Right Cessation
- 1982-02-22 IE IE370/82A patent/IE52850B1/en not_active IP Right Cessation
- 1982-02-22 NO NO820536A patent/NO154181C/en unknown
- 1982-02-22 DE DE19823206377 patent/DE3206377A1/en active Granted
- 1982-02-22 CA CA000396781A patent/CA1213097A/en not_active Expired
- 1982-02-23 FR FR828202924A patent/FR2502013B1/en not_active Expired
- 1982-02-23 IL IL65081A patent/IL65081A/en not_active IP Right Cessation
- 1982-02-23 JP JP57028040A patent/JPS57156772A/en active Granted
- 1982-02-25 MX MX191525A patent/MX163246B/en unknown
Also Published As
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US4938751A (en) | Elastomeric bladders for medical infusers | |
US2917045A (en) | Face mask and similar devices having body-conforming means | |
EP0665028A2 (en) | Apparatus for dosage of a liquid medicine | |
US3866652A (en) | Tire and wheel combination | |
US3576930A (en) | Method of preparing molded articles | |
US7294678B2 (en) | Thin walled polynitrile oxide crosslinked rubber film products and methods of manufacture thereof | |
IE42313L (en) | Tyre filled with solid polyurethane. | |
IE52850B1 (en) | Elastomeric bladders for medical infusers | |
US3983919A (en) | High-modulus rubber composition for pneumatic tires | |
US5788977A (en) | Method of making controlled release devices | |
ES8104055A1 (en) | Molding composition and method for producing a molded article. | |
US2318693A (en) | Method of shredding rubber | |
JPH05212104A (en) | Thermoplastic pharmaceutical and medical sealing article | |
JPS55152041A (en) | Production of air tire for vehicles | |
EP0257865A2 (en) | Tyre construction method | |
KR20010101378A (en) | Rubber Balloon for Ambulatory Infusion | |
JPS5634739A (en) | Composition for rubber mandrel | |
USRE30137E (en) | High-modulus rubber composition for pneumatic tires | |
JPS5618632A (en) | Rubber composition for tire bead filler | |
US1415437A (en) | Method of making tennis balls and like hollow articles | |
CA1074679A (en) | Tire composed of a first member and a cover | |
Pribylova et al. | Influence of Fillers on the Properties of Microcellular Polyurethanes | |
Bell et al. | Oxidative stress relaxation of blends of cis‐1, 4‐polybutadiene and natural rubber | |
US2270930A (en) | Production of purified cyclorubber derivatives | |
GB1293833A (en) | Process for the production of polyurethane moldings |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
MM4A | Patent lapsed |