CA1224717A - Antimicrobial compositions - Google Patents
Antimicrobial compositionsInfo
- Publication number
- CA1224717A CA1224717A CA000439002A CA439002A CA1224717A CA 1224717 A CA1224717 A CA 1224717A CA 000439002 A CA000439002 A CA 000439002A CA 439002 A CA439002 A CA 439002A CA 1224717 A CA1224717 A CA 1224717A
- Authority
- CA
- Canada
- Prior art keywords
- percent
- weight
- antimicrobial
- acrylonitrile
- butadiene
- 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.)
- Expired
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 100
- 230000000845 anti-microbial effect Effects 0.000 title claims abstract description 56
- 238000000576 coating method Methods 0.000 claims abstract description 36
- 239000011248 coating agent Substances 0.000 claims abstract description 29
- XECAHXYUAAWDEL-UHFFFAOYSA-N acrylonitrile butadiene styrene Chemical compound C=CC=C.C=CC#N.C=CC1=CC=CC=C1 XECAHXYUAAWDEL-UHFFFAOYSA-N 0.000 claims abstract description 21
- 229920000122 acrylonitrile butadiene styrene Polymers 0.000 claims abstract description 21
- 239000004676 acrylonitrile butadiene styrene Substances 0.000 claims abstract description 21
- 239000004800 polyvinyl chloride Substances 0.000 claims abstract description 18
- 229920000915 polyvinyl chloride Polymers 0.000 claims abstract description 18
- 239000004945 silicone rubber Substances 0.000 claims abstract description 11
- 229920002379 silicone rubber Polymers 0.000 claims abstract description 10
- 229910052751 metal Inorganic materials 0.000 claims abstract description 6
- 239000002184 metal Substances 0.000 claims abstract description 6
- 239000000463 material Substances 0.000 claims abstract description 5
- 150000002739 metals Chemical class 0.000 claims abstract description 4
- 229920001778 nylon Polymers 0.000 claims abstract description 4
- 239000004417 polycarbonate Substances 0.000 claims abstract description 4
- 229920000728 polyester Polymers 0.000 claims abstract description 4
- 239000004814 polyurethane Substances 0.000 claims abstract description 4
- 229920006132 styrene block copolymer Polymers 0.000 claims abstract description 4
- 239000004677 Nylon Substances 0.000 claims abstract description 3
- 239000005061 synthetic rubber Substances 0.000 claims abstract description 3
- 239000004599 antimicrobial Substances 0.000 claims description 38
- NDVLTYZPCACLMA-UHFFFAOYSA-N silver oxide Chemical group [O-2].[Ag+].[Ag+] NDVLTYZPCACLMA-UHFFFAOYSA-N 0.000 claims description 34
- 229910001923 silver oxide Inorganic materials 0.000 claims description 17
- 239000011230 binding agent Substances 0.000 claims description 6
- 150000001875 compounds Chemical class 0.000 claims description 6
- 229910052709 silver Inorganic materials 0.000 claims description 5
- 239000004332 silver Substances 0.000 claims description 5
- 229940100890 silver compound Drugs 0.000 claims description 5
- 150000003379 silver compounds Chemical class 0.000 claims description 5
- 210000002700 urine Anatomy 0.000 claims description 5
- FOIXSVOLVBLSDH-UHFFFAOYSA-N Silver ion Chemical compound [Ag+] FOIXSVOLVBLSDH-UHFFFAOYSA-N 0.000 claims description 4
- 239000011247 coating layer Substances 0.000 claims description 4
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical class [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 claims description 4
- 229910052737 gold Chemical class 0.000 claims description 4
- 239000010931 gold Chemical class 0.000 claims description 4
- 239000002245 particle Substances 0.000 claims description 4
- 150000003839 salts Chemical class 0.000 claims description 4
- 229920000515 polycarbonate Polymers 0.000 claims description 3
- 229920001194 natural rubber Polymers 0.000 abstract description 3
- 229920002635 polyurethane Polymers 0.000 abstract description 3
- 239000007787 solid Substances 0.000 abstract description 3
- 229920003051 synthetic elastomer Polymers 0.000 abstract description 3
- 229920003052 natural elastomer Polymers 0.000 abstract description 2
- 239000002904 solvent Substances 0.000 description 23
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 21
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 18
- 238000001704 evaporation Methods 0.000 description 15
- 230000008020 evaporation Effects 0.000 description 15
- 239000000843 powder Substances 0.000 description 14
- 239000007921 spray Substances 0.000 description 11
- 241000894006 Bacteria Species 0.000 description 10
- 239000011347 resin Substances 0.000 description 10
- 229920005989 resin Polymers 0.000 description 10
- FDWREHZXQUYJFJ-UHFFFAOYSA-M gold monochloride Chemical compound [Cl-].[Au+] FDWREHZXQUYJFJ-UHFFFAOYSA-M 0.000 description 9
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 9
- 150000002736 metal compounds Chemical class 0.000 description 8
- 230000002485 urinary effect Effects 0.000 description 8
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 8
- 229920002554 vinyl polymer Polymers 0.000 description 8
- 229940073584 methylene chloride Drugs 0.000 description 7
- 230000035755 proliferation Effects 0.000 description 7
- 229920006382 Lustran Polymers 0.000 description 6
- 229920003023 plastic Polymers 0.000 description 6
- 239000004033 plastic Substances 0.000 description 6
- 239000000126 substance Substances 0.000 description 6
- 208000019206 urinary tract infection Diseases 0.000 description 6
- 239000007788 liquid Substances 0.000 description 5
- 125000003545 alkoxy group Chemical group 0.000 description 4
- 238000011109 contamination Methods 0.000 description 4
- 229940009188 silver Drugs 0.000 description 4
- 210000003708 urethra Anatomy 0.000 description 4
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 3
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 3
- 229910052802 copper Inorganic materials 0.000 description 3
- 239000010949 copper Substances 0.000 description 3
- 229920000126 latex Polymers 0.000 description 3
- 230000005012 migration Effects 0.000 description 3
- 238000013508 migration Methods 0.000 description 3
- CQLFBEKRDQMJLZ-UHFFFAOYSA-M silver acetate Chemical compound [Ag+].CC([O-])=O CQLFBEKRDQMJLZ-UHFFFAOYSA-M 0.000 description 3
- 229940071536 silver acetate Drugs 0.000 description 3
- YPNVIBVEFVRZPJ-UHFFFAOYSA-L silver sulfate Chemical compound [Ag+].[Ag+].[O-]S([O-])(=O)=O YPNVIBVEFVRZPJ-UHFFFAOYSA-L 0.000 description 3
- 229910000367 silver sulfate Inorganic materials 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- 238000005507 spraying Methods 0.000 description 3
- 229910052725 zinc Inorganic materials 0.000 description 3
- 239000011701 zinc Substances 0.000 description 3
- 230000000694 effects Effects 0.000 description 2
- 229920001971 elastomer Polymers 0.000 description 2
- 229920001038 ethylene copolymer Polymers 0.000 description 2
- 230000002401 inhibitory effect Effects 0.000 description 2
- 238000000465 moulding Methods 0.000 description 2
- 239000002674 ointment Substances 0.000 description 2
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 2
- 229920001296 polysiloxane Polymers 0.000 description 2
- 230000000069 prophylactic effect Effects 0.000 description 2
- 239000005060 rubber Substances 0.000 description 2
- 210000001635 urinary tract Anatomy 0.000 description 2
- ZXSQEZNORDWBGZ-UHFFFAOYSA-N 1,3-dihydropyrrolo[2,3-b]pyridin-2-one Chemical compound C1=CN=C2NC(=O)CC2=C1 ZXSQEZNORDWBGZ-UHFFFAOYSA-N 0.000 description 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- JKFYKCYQEWQPTM-UHFFFAOYSA-N 2-azaniumyl-2-(4-fluorophenyl)acetate Chemical compound OC(=O)C(N)C1=CC=C(F)C=C1 JKFYKCYQEWQPTM-UHFFFAOYSA-N 0.000 description 1
- 208000035143 Bacterial infection Diseases 0.000 description 1
- 201000004538 Bacteriuria Diseases 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- QPLDLSVMHZLSFG-UHFFFAOYSA-N Copper oxide Chemical compound [Cu]=O QPLDLSVMHZLSFG-UHFFFAOYSA-N 0.000 description 1
- 206010064687 Device related infection Diseases 0.000 description 1
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 1
- 229910021607 Silver chloride Inorganic materials 0.000 description 1
- 229910021612 Silver iodide Inorganic materials 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 1
- KZNMRPQBBZBTSW-UHFFFAOYSA-N [Au]=O Chemical compound [Au]=O KZNMRPQBBZBTSW-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- -1 and physiological Substances 0.000 description 1
- 239000003242 anti bacterial agent Substances 0.000 description 1
- 230000000844 anti-bacterial effect Effects 0.000 description 1
- 229940088710 antibiotic agent Drugs 0.000 description 1
- 229940045985 antineoplastic platinum compound Drugs 0.000 description 1
- 208000022362 bacterial infectious disease Diseases 0.000 description 1
- 239000003899 bactericide agent Substances 0.000 description 1
- 230000003115 biocidal effect Effects 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 238000000502 dialysis Methods 0.000 description 1
- 238000003618 dip coating Methods 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- 229910001922 gold oxide Inorganic materials 0.000 description 1
- 229910001385 heavy metal Inorganic materials 0.000 description 1
- 208000015181 infectious disease Diseases 0.000 description 1
- 230000005764 inhibitory process Effects 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 230000002262 irrigation Effects 0.000 description 1
- 238000003973 irrigation Methods 0.000 description 1
- 230000005923 long-lasting effect Effects 0.000 description 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 229910021645 metal ion Inorganic materials 0.000 description 1
- 229920006173 natural rubber latex Polymers 0.000 description 1
- 239000011664 nicotinic acid Substances 0.000 description 1
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- 150000003058 platinum compounds Chemical class 0.000 description 1
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
- 239000004926 polymethyl methacrylate Substances 0.000 description 1
- 239000010970 precious metal Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 238000011321 prophylaxis Methods 0.000 description 1
- 229920002631 room-temperature vulcanizate silicone Polymers 0.000 description 1
- 229910001958 silver carbonate Inorganic materials 0.000 description 1
- LKZMBDSASOBTPN-UHFFFAOYSA-L silver carbonate Substances [Ag].[O-]C([O-])=O LKZMBDSASOBTPN-UHFFFAOYSA-L 0.000 description 1
- 229940071575 silver citrate Drugs 0.000 description 1
- 229940045105 silver iodide Drugs 0.000 description 1
- HKZLPVFGJNLROG-UHFFFAOYSA-M silver monochloride Chemical compound [Cl-].[Ag+] HKZLPVFGJNLROG-UHFFFAOYSA-M 0.000 description 1
- CLDWGXZGFUNWKB-UHFFFAOYSA-M silver;benzoate Chemical compound [Ag+].[O-]C(=O)C1=CC=CC=C1 CLDWGXZGFUNWKB-UHFFFAOYSA-M 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- QUTYHQJYVDNJJA-UHFFFAOYSA-K trisilver;2-hydroxypropane-1,2,3-tricarboxylate Chemical compound [Ag+].[Ag+].[Ag+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O QUTYHQJYVDNJJA-UHFFFAOYSA-K 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/18—Oxygen-containing compounds, e.g. metal carbonyls
- C08K3/20—Oxides; Hydroxides
- C08K3/22—Oxides; Hydroxides of metals
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS 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
- A61L29/00—Materials for catheters, medical tubing, cannulae, or endoscopes or for coating catheters
- A61L29/14—Materials characterised by their function or physical properties, e.g. lubricating compositions
- A61L29/16—Biologically active materials, e.g. therapeutic substances
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/10—Metal compounds
- C08K3/105—Compounds containing metals of Groups 1 to 3 or of Groups 11 to 13 of the Periodic Table
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS 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
- A61L2300/00—Biologically active materials used in bandages, wound dressings, absorbent pads or medical devices
- A61L2300/10—Biologically active materials used in bandages, wound dressings, absorbent pads or medical devices containing or releasing inorganic materials
- A61L2300/102—Metals or metal compounds, e.g. salts such as bicarbonates, carbonates, oxides, zeolites, silicates
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS 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
- A61L2300/00—Biologically active materials used in bandages, wound dressings, absorbent pads or medical devices
- A61L2300/10—Biologically active materials used in bandages, wound dressings, absorbent pads or medical devices containing or releasing inorganic materials
- A61L2300/102—Metals or metal compounds, e.g. salts such as bicarbonates, carbonates, oxides, zeolites, silicates
- A61L2300/104—Silver, e.g. silver sulfadiazine
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Biomedical Technology (AREA)
- Engineering & Computer Science (AREA)
- Molecular Biology (AREA)
- Epidemiology (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Materials For Medical Uses (AREA)
Abstract
ANTIMICROBIAL COMPOSITIONS
Abstract of the Invention Antimicrobial compositions finding particular utility for coating access systems, lead devices including shunts, cannulae, catheters (18), catheter adapters, wires and other solid or hollow tubular devices used for a variety of medical purposes is provided. The composition comprises a material se-lected from the group consisting of acrylonitrile-butadiene-styrene copolymers, polyvinyl chloride, mixtures thereof, polyesters, polyurethanes, styrene-block copolymers, natural and synthetic rubbers, poly-carbonates, nylon and silicone rubber mixed with an oligodynamic material consisting essentially of phy-siological, antimicrobial metals.
Abstract of the Invention Antimicrobial compositions finding particular utility for coating access systems, lead devices including shunts, cannulae, catheters (18), catheter adapters, wires and other solid or hollow tubular devices used for a variety of medical purposes is provided. The composition comprises a material se-lected from the group consisting of acrylonitrile-butadiene-styrene copolymers, polyvinyl chloride, mixtures thereof, polyesters, polyurethanes, styrene-block copolymers, natural and synthetic rubbers, poly-carbonates, nylon and silicone rubber mixed with an oligodynamic material consisting essentially of phy-siological, antimicrobial metals.
Description
12Z~7~
ANTIMICROBIA_OMPOSITIONS
Field of the Invention This invention relates to compositions useful in making medical devices and useful in providing antimi-crobial coatings on medical devices. The invention particularly relates to antimicrobial compositions use-ful as coatings for medical connection devices and for making medical connection devices which are susceptible to touch contamination. These compositions are also useful as antimicrobial coatings for access systems and lead devices (for example, shunts, cannulae, catheters, wires, enteral feeding tubes, endotracheal tubes, per-cutaneous devices and other solid or hollow tubular devices) used for a variety of medical purposes. In addition, the compositions may be used as antimicrobial coatings for wound coverings or in the manufacture of thin, flexible, skin-like wound coverings.
Background of the Invention Indwelling urethral catheterization is performed in approximately 10 to 15 percent of hospitalized patients.
About 25 percent of these patients contract bacterial infections of the urinary tract. Two studies of note are, Garibaldi, R. A.; Burke, J. P.; Dickman, M. L.;
and Smith, C. B., "Factors Predisposing to Bacteriuria During Indwelling Urethral Cathiterization". New Engl.
J. Med., 291:215, 1974 and Kunin, C. M. and McCormack, R. C., "Prevention of Catheter-Induced Urinary-Tract Infections by Sterile Closed Drainage". New Engl. J.
Med., 274:1155, 1966.
The incidence of catheter-induced urinary tract infection still remains a problem despite various pro-phylactic measures that have been tried. Attempts to ~z2~7~7~
reduce the incidence of urinary tract infections have included the application of antibiotic ointments or other bactericidal agents to the surface of the cathe-ter, frequent bladder irrigation with concommittant prophylactic administration of antibiotics, or inhibi-tion of the growth of bacteria in urine drainage con-tainers. See, Akiyama, H. and Okamoto, S., "Prophylaxis of Indwelling Urethral Catheter Infection: Clinical Experience with a Modified Foley Catheter and Drainage System". The Journal of Urologv, 121:40, 1979. United States Patent No. 4,054,139, OligodYnamic Catheter, to Crossley, teaches a catheter, or the like, which com-prises an oligodynamic agent such as metallic silver or its compounds, alone or in association with other heavy metals such as gold, for the purpose of reducing infection associated with these devices.
It would be desirable to pro~ide compositions use-ful as coatings for urinary catheters, lead devices, medical connections susceptible to touch contamination and the like, and compositions useful as a material for making these various devices, whereby the proli-feration of bacteria thereon or in relatively close proximity thereto is inhibited. Inhibiting the proli-feration of bacteria on urinary catheters and catheter adapter connections would reduce the risk of urinary tract infections caused by bacteria accessing the urinary tract at these sites. It also would be de-sirable for the compositions to be easily applied as coatings on presently existing medical connections and devices. A desirable characteristic of such a composition would be an antimicrobial effect which is long lasting without being physiologically incompatible with nearby tissue.
1~47~7 Summary of the Invention Varlous aspects of the invention are as follows:
An antimicrobial composition comprising:
30 to 85 percent by weight of a binder consisting essentially of a material selected from the group consisting of acrylonitrile-butadiene-styrene copolymers, polyvinyl chloride, mixtures thereof, polyesters, polyurethanes, styrene-block copolymers, natural and synthetic rubbers, polycarbonates, nylon and silicone rubber; and, 15 to 70 percent by weight of an antimicrobial agent selected from the group consisting of compounds of physio-logical, antimicrobial metals and mixtures thereof.
An antimicrobial composition for coating articles comprising:
30 to 85 percent by weight of a binder consisting essentially of acrylonitrile-butadiene-styrene copolymers;
and, 15 to 70 percent by weight of an antimicrobial agent selected from the group consisting essentially of silver compounds and mixtures thereof whereby the particles of silver compound are exposed on the coating layer on the surface of the article and being sufficiently mobile to produce, within 24 hours, a solution of at least 10 6 molar concentration of silver ion concentration in a stagnant film of urine in contact with said surface.
An antimicrobial composition for coating articles comprising:
30 to 85 percent by weight of a binder consisting essentially of a mixture consisting of 35 to 65 percent by weight of acrylonitrile-butadiene-styrene copolymers and 35 to 65 percent by weight of polyvinyl chloride; and, 15 to 70 percent by weight of an antimicrobial agent consisting essentially of silver oxide whereby the particles of silver oxide are exposed on the coating layer on the outermost surface of the article and being sufficiently mobile to produce, within 24 hours, a solution of at least 10 6 molar concentration of silver ion concentration in a stagnant film of urine in contact with said surface.
`~
~ZZ'~717 ~escription of the Inventio In accordance with this inventionr antimicrobial compositions are provided which find particular utility as coatings which inhibit the proliferation of bacteria 5 near the surface of urinary catheters and th~ connec-tion between the catheter and the drainage tube, namely, the catheter/catheter adapter ~unction site. Thc anti-microbial coating on the catheter inhibits the prolifera-tion of bacteria in the area between the catheter and ~0 the walls of the urethra, and the antibacterial coatinq on the catheter adapter inhibits the pro1iferation of bacteria in the closed area connecting the catheter and the catheter adapter.
Catheters implanted in patients undergoing con-15 tinuous ambulatory peritoneal dialysis also can becoated with an antimicrohial composition of this in-vention. P.n antimicrobial composition Or this inven-tion can be applied as a coatin~ to medical shunts !
cannulae, catheters, wires and other solid or ~ollow 20 tuhular devices used for medical purposes.
Preferably, the coating using an antimicrobia~
co~position is prepared by mixing a suitable resin and a co~pound of a physiological, antimicrobial metal in an appropriate solvent for the resin. The solvent 25 should not adversely effect the activity of the metal compound as an antimicrobial agent. The coatinq can be applied to a medica~ device by di~ping in the mix-ture of resin, solvent, and physiological, antimicro-bial metal compound and thereafter allowina the solvent 30 to evaporate. Both inside and outside surfaces may be coated. Alternatively, the medical articles may be sprayed with the mixture and the solvent allowed to evaporate. Where appropriate, particularly with a latex rubber resin, a volatile liquid carrier may be - ~2247~7 used with the resin dispersed in the volatile liquid.
An article may be dipped or sprayed with this prepara-tion. upon evaporation of the volatile liquid and curing of the resin a coating for the article is pro-vided.
Indeed, articles can be made from a composition of a suitable resin and a compound of physiological, antimicrobial metal by molding the composition to form the article.
The resins used in formulating the mixture include, for example, acrylonitrile-butadiene-styrene copolymer, rigid polyvinyl chloride, curable silicones, alkoxy cured RTV silicone rubber, polyesters, rubber latexes (e.g., natural or synthetic polyisoprene), polyurethanes, styrene-block copolymers (e.g., Kraton-D*and Kraton-5*, manufactured by Shell), ethylene copolymers (e.g., vinyl acetate, ethyl acrylate, or mixtures thereof), ethylene copolymers of maleic anhydride, acrylic acid or both, polycarbonates, nylons, and polymethyl methacrylate.
Into a mixture of resin and solvent is added a quantity of physiological, antimicrobial metal compound.
Alternatively, a quantity of physiological, antimicro-bial metal compound may be mixed with a resin for direct molding of an article. Physiological, antimicrobial metals are meant to include the precious metals, such as silver, gold and platinum, and copper and zinc.
Physiological, antimicrobial metal compounds used herein include oxides and salts of preferably silver and also gold, for example: silver acetate, silver benzoate, silver carbonate, silver citrate, silver chloride, sil-ver iodide, silver oxide, silver sulfate, gold chloride and gold oxide. Platinum compounds such as chloropla-tinic acid or its salts (e.g., sodium and calcium chlo-roplatinate) may also be used. Also, compounds of * trade marks 1224~7 copper and zinc may be used, for example: oxides and salts of copper and zinc such as those indicated above for silver. Single physiological, antimicrobial metal compounds or combinations of physiological, antimicrobial metal compounds may be used.
Preferred physiological, antimicrobial metal compounds used in this invention are silver acetate, silver oxide, silver sulfate, gold chloride and a combination of silver oxide and gold chloride. Pre-ferred quantities of physiological, antimicrobialmetal compound are those sufficient to produce, within a 24 hour period, a solution of at least 10 6 molar concentration of metal ion concentration in a stagnant film of liquid in contact with a surface of an article made from a composition of this invention or an article coated with a composition of this invention.
~2Z4717 Brief Description of the Drawings For a more complete under~tanding of this inven-tion, reference should now be had to the embodiments illustrated in greater detail in the accompanying drawings.
In the drawings:
Figure 1 is an elevational view of a catheter adapter showing one end coated with an antimicrobial composition of this invention.
Figure 2 is an elevational view of a Foley catheter showing the portion of the catheter typically inserted into the urethra, coated with an antimicrobial compo-sition of this invention.
Figure 3 is a perspective view of the catheter adapter of this invention shown connecting a urinary drainage tube and a catheter.
~2Z'~717 Detailed Description of the Drawings Turning now to the drawings, Figure 1 shows a conventional catheter adapter 10 after it has been coated with an antimicrobial composition of this in-vention. Catheter adapter 10 has drainage tube end 12, catheter end 14, and injection site 16.
Catheter end 14 is spray coated or dip coated with an antimicrobial composition of this invention. The shaded portion of catheter end 14 is illustrative of the coating.
Figure 2 shows urinary catheter 18. Catheter 18 has drainage connection 20 and inflation connection 22 for inflating the catheter balloon.
The shaded portion of catheter 18 illustrates the area coated by an antimicrobial composition of this invention. Typically, this coating will be applied to that portion of catheter 18 which resides in the urethra of a patient.
A typical connection of catheter adapter 10 is illustrated in Figure 3. Catheter adapter 10 has the coated catheter end 14 connected to drainage connec-tion 20 of the catheter. Drainage tube end 12 is connected to drainage tube 24 to complete the connec-tion. Drainage tube 24 drains into a urinary drainage bag (not shown).
The risk of touch contamination of catheter end 14 is reduced by coating catheter end 14 of catheter adapter 10 with an antimicrobial composition of the present invention. Reducing the risk of touch contami-nation of catheter end 14 reduces the risk of subsequent urinary tract infection caused by a contaminated catheter adapter.
The antimicrobial composition coating catheter 18 inhibits the proliferation and migration of bacteria ~224717 in a stagnant film between the coated catheter walls and the walls of the urethra. By inhibiting the pro-liferation and migration of bacteria through this route, subsequent urinary tract infection caused by such proliferation and migration of bacteria is re-duced.
The examples below are offered for illustrative purposes only and are not intended to limit the scope of the invention of this application, which is as de-fined in the claims below.
A mixture was made of 50 milliliters of methylenechloride, 5 grams of acrylonitrile-butadiene-styrene copolymer (LUSTRAN 240-29, a trademark of the Monsanto Company), and 1.2 grams of silver oxide powder. The mixture was stirred for approximately one hour. A
polyvinyl chloride catheter adapter, used to connect a urinary catheter and drainage tubing for a urinary drainage connector, was coated on the exterior and the interior by dipping the connector into the mixture.
Upon evaporation of the solvent, an antimicrobial coat-ing remained bonded to the catheter adapter. Catheter adapters can also be sprayed with the mixture.
A mixture was made by combining 50 milliliters of tetrahydrofuran, 5 grams of polyvinyl chloride (Alpha Plastics and Chemicals, clear rigid vinyl 2212/7-118), and 1.2 grams of silver oxide powder. The mixture was stirred for about one hour.
Vinyl compatible catheter adapters may be either dip coated or spray coated with this mixture. By dip coating the catheter adapter, the exterior and interior ~ZZ~717 surfaces may be conveniently coated. Upon ev~poration of the solvent, tetrahydrofuran, an antimicrobial coat-ing will remain bonded to the device.
Equivalent results may be obtained when a mixture is made by combining 25 milliliters of tetrahydrofuran, 25 milliliters of methylene chloride, 2.5 grams of acrylonitrile-butadiene-styrene copolymer (LUSTR~I
240-29), 2.5 grams of polyvinyl chloride (Alpha Plastics and Chemicals, clear rigid vinyl 2212/7-118), and 1.2 grams of silver oxide powder. The mixture may be stirred for about one hour.
A catheter adapter may be either dip coated or spray coated with this mixture. Upon evaporation of the solvents, an antimicrobial coating will remain bonded to the device.
A mixture was made by combining 10 milliliters of alkoxy curing RTV rubber, 65 milliliters of FREON TF
solvent (FREON is a trademark of E. I. du pont de Nemours & Co.), and 5 grams of silver oxide powder. The mixture was stirred for about one hour.
A silicone rubber Foley catheter was dipped into this mixture and upon evaporation of the solvent and curing of the RTV, a flexible, antimicrobial coating on the interior and exterior surfaces of the silicone rubber catheter was provided. The coating adhered well to the catheter. Spray coating of the catheter is a viable alternative.
A mixture was made by combining 100 milliliters lZZ47~
of tetrahydrofuran, 5 grams of acrylonitrile-butadiene-styrene copolymer (LUSTRAN 240-29), and 1 gram of silver acetate. The mixture was stirred for about one hour.
Acrylonitrile-butadiene-styrene compatible devices may be spray or dip coated with the mixture. Upon evapora-tion of the solvent, an antimicrobial coating will remain on the device.
Equivalent results may be obtained when a mixture is made by combining 100 milliliters of methylene chlo-ride, 5 gra~s of acrylonitrile-butadiene-styrene copoly-mer (LUSTRAN 240-29), and 1 gram of silver sulfate. The mixture may be stirred for about one hour. Acrylonitrile-butadiene-styrene compatible devices may be spray or dip coated with the mixture. Upon evaporation of the solvent, an antimicrobial coating will remain on the device.
EXA~PLE 7 Equivalent results may be obtained when a mixture is made by combining 50 milliliters of tetrahydrofuran, 5 grams of polyvinyl chloride (Alpha Plastics and Chemicals, clear rigid vinyl 2212/7-118), and 1.2 grams of gold chloride powder. The mixture may be stirred for about one hour. Polyvinyl chloride compatible de-vices may be spray or dip coated with the mixture. Upon evaporation of the solvent, an antimicrobial coating will remain on the device.
Equivalent results may be obtained when a mixture is made by combining 25 milliliters of tetrahydrofuran, 25 milliliters of methylene chloride, 2.5 grams of acrylonitrile-butadiene-styrene copolymer tLUSTRAN
~22~17 240-29), 2.5 grams of polyvinyl chloride (Alpha Plastics and Chemicals, clear rigid vinyl 2212/7-118), and 1.2 grams of gold chloride powder. The mixture may be stirred for about one hour. Devices may be either dip coated or spray coated with this mixture. Upon evaporation of the solvents, an antimicrobial coating remains bonded to the device.
Equivalent results may be obtained when a mixture is made by combining 10 milliliters of alkoxy curing RTV, 65 milliliters of FREON TF solvent and 5 grams of gold chloride powder. The mixture may be stirred for about one hour.
A silicone rubber Foley catheter or other silicone lS rubber medical device mav be dipped into this mixture and upon evaporation of the solvent and curing of the RTV, a flexible, antimicrobial coating for the silicone rubber catheter will be provided. Spray coating of the catheter is also a viable alternative.
Equivalent results may be obtained when a mixture is made by combining 50 milliliters of tetrahydrofuran, 5 grams of polyvinyl chloride (Alpha Plastics and Chemicals, clear rigid vinyl 2212/7-118), 1.2 grams of silver oxide powder, and 0.1 gram of gold chloride powder. The mixture may be stirred for about one hour.
Vinyl compatible catheter adapters or other medi-cal devices may be either dip coated or spray coated with this mixture. Upon evaporation of the solvent, tetrahydrofuran, an antimicrobial coating will remain on the device.
~224717 Equivalent results may be obtained when a mixture is made by combining 25 milliliters of tetrahydrofuran, 25 milliliters of methylene chloride, 2.5 grams of acrylonitrile-butadiene-stryrene copolymer (LUSTRAN
240-29), 2.5 grams of polyvinyl chloride (Alpha Plastics and Chemicals, clear rigid vinyl 2212/7-ll~), 1.2 grams of silver oxide powder, and 0.1 gram of gold chloride powder. The mixture may be stirred for about one hour.
Devices may be either dip coated or spray coated with this mixture. Upon evaporation of the solvents, an antimicrobial coating will remain on the device.
Equivalent results may be obtained when a mixture is made by combining 10 milliliters of alkoxy curing RTV, 65 milliliters of FREON TF solvent, 5 grams of silver oxide powder, and 0.5 gram of gold chloride powder. The mixture may be stirred for about one hour.
A silicone rubber Foley catheter or other silicone rubber medical device may be dipped into this mixture and upon evaporation of the solvent and curing of the RTV, a flexible, antimicrobial coating for the silicone rubber catheter is provided. Spray coating of the catheter is also an alternative application means.
Equivalent results may be obtained when a mixture is made by combining 100 milliliters of natural rubber latex with 10 grams of silver oxide powder. The mixture may be stirred until the silver oxide is dispersed.
Cured latex rubber devices may be dip coated with this ~2Z~7~7 mixture. Upon evaporation of the volatile liquid car-rier and curing of the coating mixture, an antimicrobial coating having high elastomeric characteristics will remain adhered to the device.
Equivalent results may be obtained when a mixture is made by combining 50 milliliters of methylene chlo-ride, 5 grams of acrylonitrile-butadiene-styrene copoly-mer (LUSTRAN 240-29), and 1.2 grams of copper oxide powder. The mixture may be stirred for about one hour.
A catheter adapter may be either dip coated or spray coated with this mixture. Upon evaporation of the solvent, an antimicrobial coating will remain bonded to the device.
Equivalent results may be obtained when a mixture is made by combining 50 milliliters of methylene chlo-ride, 5 grams of acrylonitrile-butadiene-styrene copoly-mer (LUSTRAN 240-29), and 1.2 grams of zinc oxide powder.
The mixture may be stirred for about one hour. A cathe-ter adapter may be either dip coated or spray coated with this mixture. Upon evaporation of the solvent, an antimicrobial coating will remain bonded to the de-vlce .
WHAT IS CLAIMED IS:
ANTIMICROBIA_OMPOSITIONS
Field of the Invention This invention relates to compositions useful in making medical devices and useful in providing antimi-crobial coatings on medical devices. The invention particularly relates to antimicrobial compositions use-ful as coatings for medical connection devices and for making medical connection devices which are susceptible to touch contamination. These compositions are also useful as antimicrobial coatings for access systems and lead devices (for example, shunts, cannulae, catheters, wires, enteral feeding tubes, endotracheal tubes, per-cutaneous devices and other solid or hollow tubular devices) used for a variety of medical purposes. In addition, the compositions may be used as antimicrobial coatings for wound coverings or in the manufacture of thin, flexible, skin-like wound coverings.
Background of the Invention Indwelling urethral catheterization is performed in approximately 10 to 15 percent of hospitalized patients.
About 25 percent of these patients contract bacterial infections of the urinary tract. Two studies of note are, Garibaldi, R. A.; Burke, J. P.; Dickman, M. L.;
and Smith, C. B., "Factors Predisposing to Bacteriuria During Indwelling Urethral Cathiterization". New Engl.
J. Med., 291:215, 1974 and Kunin, C. M. and McCormack, R. C., "Prevention of Catheter-Induced Urinary-Tract Infections by Sterile Closed Drainage". New Engl. J.
Med., 274:1155, 1966.
The incidence of catheter-induced urinary tract infection still remains a problem despite various pro-phylactic measures that have been tried. Attempts to ~z2~7~7~
reduce the incidence of urinary tract infections have included the application of antibiotic ointments or other bactericidal agents to the surface of the cathe-ter, frequent bladder irrigation with concommittant prophylactic administration of antibiotics, or inhibi-tion of the growth of bacteria in urine drainage con-tainers. See, Akiyama, H. and Okamoto, S., "Prophylaxis of Indwelling Urethral Catheter Infection: Clinical Experience with a Modified Foley Catheter and Drainage System". The Journal of Urologv, 121:40, 1979. United States Patent No. 4,054,139, OligodYnamic Catheter, to Crossley, teaches a catheter, or the like, which com-prises an oligodynamic agent such as metallic silver or its compounds, alone or in association with other heavy metals such as gold, for the purpose of reducing infection associated with these devices.
It would be desirable to pro~ide compositions use-ful as coatings for urinary catheters, lead devices, medical connections susceptible to touch contamination and the like, and compositions useful as a material for making these various devices, whereby the proli-feration of bacteria thereon or in relatively close proximity thereto is inhibited. Inhibiting the proli-feration of bacteria on urinary catheters and catheter adapter connections would reduce the risk of urinary tract infections caused by bacteria accessing the urinary tract at these sites. It also would be de-sirable for the compositions to be easily applied as coatings on presently existing medical connections and devices. A desirable characteristic of such a composition would be an antimicrobial effect which is long lasting without being physiologically incompatible with nearby tissue.
1~47~7 Summary of the Invention Varlous aspects of the invention are as follows:
An antimicrobial composition comprising:
30 to 85 percent by weight of a binder consisting essentially of a material selected from the group consisting of acrylonitrile-butadiene-styrene copolymers, polyvinyl chloride, mixtures thereof, polyesters, polyurethanes, styrene-block copolymers, natural and synthetic rubbers, polycarbonates, nylon and silicone rubber; and, 15 to 70 percent by weight of an antimicrobial agent selected from the group consisting of compounds of physio-logical, antimicrobial metals and mixtures thereof.
An antimicrobial composition for coating articles comprising:
30 to 85 percent by weight of a binder consisting essentially of acrylonitrile-butadiene-styrene copolymers;
and, 15 to 70 percent by weight of an antimicrobial agent selected from the group consisting essentially of silver compounds and mixtures thereof whereby the particles of silver compound are exposed on the coating layer on the surface of the article and being sufficiently mobile to produce, within 24 hours, a solution of at least 10 6 molar concentration of silver ion concentration in a stagnant film of urine in contact with said surface.
An antimicrobial composition for coating articles comprising:
30 to 85 percent by weight of a binder consisting essentially of a mixture consisting of 35 to 65 percent by weight of acrylonitrile-butadiene-styrene copolymers and 35 to 65 percent by weight of polyvinyl chloride; and, 15 to 70 percent by weight of an antimicrobial agent consisting essentially of silver oxide whereby the particles of silver oxide are exposed on the coating layer on the outermost surface of the article and being sufficiently mobile to produce, within 24 hours, a solution of at least 10 6 molar concentration of silver ion concentration in a stagnant film of urine in contact with said surface.
`~
~ZZ'~717 ~escription of the Inventio In accordance with this inventionr antimicrobial compositions are provided which find particular utility as coatings which inhibit the proliferation of bacteria 5 near the surface of urinary catheters and th~ connec-tion between the catheter and the drainage tube, namely, the catheter/catheter adapter ~unction site. Thc anti-microbial coating on the catheter inhibits the prolifera-tion of bacteria in the area between the catheter and ~0 the walls of the urethra, and the antibacterial coatinq on the catheter adapter inhibits the pro1iferation of bacteria in the closed area connecting the catheter and the catheter adapter.
Catheters implanted in patients undergoing con-15 tinuous ambulatory peritoneal dialysis also can becoated with an antimicrohial composition of this in-vention. P.n antimicrobial composition Or this inven-tion can be applied as a coatin~ to medical shunts !
cannulae, catheters, wires and other solid or ~ollow 20 tuhular devices used for medical purposes.
Preferably, the coating using an antimicrobia~
co~position is prepared by mixing a suitable resin and a co~pound of a physiological, antimicrobial metal in an appropriate solvent for the resin. The solvent 25 should not adversely effect the activity of the metal compound as an antimicrobial agent. The coatinq can be applied to a medica~ device by di~ping in the mix-ture of resin, solvent, and physiological, antimicro-bial metal compound and thereafter allowina the solvent 30 to evaporate. Both inside and outside surfaces may be coated. Alternatively, the medical articles may be sprayed with the mixture and the solvent allowed to evaporate. Where appropriate, particularly with a latex rubber resin, a volatile liquid carrier may be - ~2247~7 used with the resin dispersed in the volatile liquid.
An article may be dipped or sprayed with this prepara-tion. upon evaporation of the volatile liquid and curing of the resin a coating for the article is pro-vided.
Indeed, articles can be made from a composition of a suitable resin and a compound of physiological, antimicrobial metal by molding the composition to form the article.
The resins used in formulating the mixture include, for example, acrylonitrile-butadiene-styrene copolymer, rigid polyvinyl chloride, curable silicones, alkoxy cured RTV silicone rubber, polyesters, rubber latexes (e.g., natural or synthetic polyisoprene), polyurethanes, styrene-block copolymers (e.g., Kraton-D*and Kraton-5*, manufactured by Shell), ethylene copolymers (e.g., vinyl acetate, ethyl acrylate, or mixtures thereof), ethylene copolymers of maleic anhydride, acrylic acid or both, polycarbonates, nylons, and polymethyl methacrylate.
Into a mixture of resin and solvent is added a quantity of physiological, antimicrobial metal compound.
Alternatively, a quantity of physiological, antimicro-bial metal compound may be mixed with a resin for direct molding of an article. Physiological, antimicrobial metals are meant to include the precious metals, such as silver, gold and platinum, and copper and zinc.
Physiological, antimicrobial metal compounds used herein include oxides and salts of preferably silver and also gold, for example: silver acetate, silver benzoate, silver carbonate, silver citrate, silver chloride, sil-ver iodide, silver oxide, silver sulfate, gold chloride and gold oxide. Platinum compounds such as chloropla-tinic acid or its salts (e.g., sodium and calcium chlo-roplatinate) may also be used. Also, compounds of * trade marks 1224~7 copper and zinc may be used, for example: oxides and salts of copper and zinc such as those indicated above for silver. Single physiological, antimicrobial metal compounds or combinations of physiological, antimicrobial metal compounds may be used.
Preferred physiological, antimicrobial metal compounds used in this invention are silver acetate, silver oxide, silver sulfate, gold chloride and a combination of silver oxide and gold chloride. Pre-ferred quantities of physiological, antimicrobialmetal compound are those sufficient to produce, within a 24 hour period, a solution of at least 10 6 molar concentration of metal ion concentration in a stagnant film of liquid in contact with a surface of an article made from a composition of this invention or an article coated with a composition of this invention.
~2Z4717 Brief Description of the Drawings For a more complete under~tanding of this inven-tion, reference should now be had to the embodiments illustrated in greater detail in the accompanying drawings.
In the drawings:
Figure 1 is an elevational view of a catheter adapter showing one end coated with an antimicrobial composition of this invention.
Figure 2 is an elevational view of a Foley catheter showing the portion of the catheter typically inserted into the urethra, coated with an antimicrobial compo-sition of this invention.
Figure 3 is a perspective view of the catheter adapter of this invention shown connecting a urinary drainage tube and a catheter.
~2Z'~717 Detailed Description of the Drawings Turning now to the drawings, Figure 1 shows a conventional catheter adapter 10 after it has been coated with an antimicrobial composition of this in-vention. Catheter adapter 10 has drainage tube end 12, catheter end 14, and injection site 16.
Catheter end 14 is spray coated or dip coated with an antimicrobial composition of this invention. The shaded portion of catheter end 14 is illustrative of the coating.
Figure 2 shows urinary catheter 18. Catheter 18 has drainage connection 20 and inflation connection 22 for inflating the catheter balloon.
The shaded portion of catheter 18 illustrates the area coated by an antimicrobial composition of this invention. Typically, this coating will be applied to that portion of catheter 18 which resides in the urethra of a patient.
A typical connection of catheter adapter 10 is illustrated in Figure 3. Catheter adapter 10 has the coated catheter end 14 connected to drainage connec-tion 20 of the catheter. Drainage tube end 12 is connected to drainage tube 24 to complete the connec-tion. Drainage tube 24 drains into a urinary drainage bag (not shown).
The risk of touch contamination of catheter end 14 is reduced by coating catheter end 14 of catheter adapter 10 with an antimicrobial composition of the present invention. Reducing the risk of touch contami-nation of catheter end 14 reduces the risk of subsequent urinary tract infection caused by a contaminated catheter adapter.
The antimicrobial composition coating catheter 18 inhibits the proliferation and migration of bacteria ~224717 in a stagnant film between the coated catheter walls and the walls of the urethra. By inhibiting the pro-liferation and migration of bacteria through this route, subsequent urinary tract infection caused by such proliferation and migration of bacteria is re-duced.
The examples below are offered for illustrative purposes only and are not intended to limit the scope of the invention of this application, which is as de-fined in the claims below.
A mixture was made of 50 milliliters of methylenechloride, 5 grams of acrylonitrile-butadiene-styrene copolymer (LUSTRAN 240-29, a trademark of the Monsanto Company), and 1.2 grams of silver oxide powder. The mixture was stirred for approximately one hour. A
polyvinyl chloride catheter adapter, used to connect a urinary catheter and drainage tubing for a urinary drainage connector, was coated on the exterior and the interior by dipping the connector into the mixture.
Upon evaporation of the solvent, an antimicrobial coat-ing remained bonded to the catheter adapter. Catheter adapters can also be sprayed with the mixture.
A mixture was made by combining 50 milliliters of tetrahydrofuran, 5 grams of polyvinyl chloride (Alpha Plastics and Chemicals, clear rigid vinyl 2212/7-118), and 1.2 grams of silver oxide powder. The mixture was stirred for about one hour.
Vinyl compatible catheter adapters may be either dip coated or spray coated with this mixture. By dip coating the catheter adapter, the exterior and interior ~ZZ~717 surfaces may be conveniently coated. Upon ev~poration of the solvent, tetrahydrofuran, an antimicrobial coat-ing will remain bonded to the device.
Equivalent results may be obtained when a mixture is made by combining 25 milliliters of tetrahydrofuran, 25 milliliters of methylene chloride, 2.5 grams of acrylonitrile-butadiene-styrene copolymer (LUSTR~I
240-29), 2.5 grams of polyvinyl chloride (Alpha Plastics and Chemicals, clear rigid vinyl 2212/7-118), and 1.2 grams of silver oxide powder. The mixture may be stirred for about one hour.
A catheter adapter may be either dip coated or spray coated with this mixture. Upon evaporation of the solvents, an antimicrobial coating will remain bonded to the device.
A mixture was made by combining 10 milliliters of alkoxy curing RTV rubber, 65 milliliters of FREON TF
solvent (FREON is a trademark of E. I. du pont de Nemours & Co.), and 5 grams of silver oxide powder. The mixture was stirred for about one hour.
A silicone rubber Foley catheter was dipped into this mixture and upon evaporation of the solvent and curing of the RTV, a flexible, antimicrobial coating on the interior and exterior surfaces of the silicone rubber catheter was provided. The coating adhered well to the catheter. Spray coating of the catheter is a viable alternative.
A mixture was made by combining 100 milliliters lZZ47~
of tetrahydrofuran, 5 grams of acrylonitrile-butadiene-styrene copolymer (LUSTRAN 240-29), and 1 gram of silver acetate. The mixture was stirred for about one hour.
Acrylonitrile-butadiene-styrene compatible devices may be spray or dip coated with the mixture. Upon evapora-tion of the solvent, an antimicrobial coating will remain on the device.
Equivalent results may be obtained when a mixture is made by combining 100 milliliters of methylene chlo-ride, 5 gra~s of acrylonitrile-butadiene-styrene copoly-mer (LUSTRAN 240-29), and 1 gram of silver sulfate. The mixture may be stirred for about one hour. Acrylonitrile-butadiene-styrene compatible devices may be spray or dip coated with the mixture. Upon evaporation of the solvent, an antimicrobial coating will remain on the device.
EXA~PLE 7 Equivalent results may be obtained when a mixture is made by combining 50 milliliters of tetrahydrofuran, 5 grams of polyvinyl chloride (Alpha Plastics and Chemicals, clear rigid vinyl 2212/7-118), and 1.2 grams of gold chloride powder. The mixture may be stirred for about one hour. Polyvinyl chloride compatible de-vices may be spray or dip coated with the mixture. Upon evaporation of the solvent, an antimicrobial coating will remain on the device.
Equivalent results may be obtained when a mixture is made by combining 25 milliliters of tetrahydrofuran, 25 milliliters of methylene chloride, 2.5 grams of acrylonitrile-butadiene-styrene copolymer tLUSTRAN
~22~17 240-29), 2.5 grams of polyvinyl chloride (Alpha Plastics and Chemicals, clear rigid vinyl 2212/7-118), and 1.2 grams of gold chloride powder. The mixture may be stirred for about one hour. Devices may be either dip coated or spray coated with this mixture. Upon evaporation of the solvents, an antimicrobial coating remains bonded to the device.
Equivalent results may be obtained when a mixture is made by combining 10 milliliters of alkoxy curing RTV, 65 milliliters of FREON TF solvent and 5 grams of gold chloride powder. The mixture may be stirred for about one hour.
A silicone rubber Foley catheter or other silicone lS rubber medical device mav be dipped into this mixture and upon evaporation of the solvent and curing of the RTV, a flexible, antimicrobial coating for the silicone rubber catheter will be provided. Spray coating of the catheter is also a viable alternative.
Equivalent results may be obtained when a mixture is made by combining 50 milliliters of tetrahydrofuran, 5 grams of polyvinyl chloride (Alpha Plastics and Chemicals, clear rigid vinyl 2212/7-118), 1.2 grams of silver oxide powder, and 0.1 gram of gold chloride powder. The mixture may be stirred for about one hour.
Vinyl compatible catheter adapters or other medi-cal devices may be either dip coated or spray coated with this mixture. Upon evaporation of the solvent, tetrahydrofuran, an antimicrobial coating will remain on the device.
~224717 Equivalent results may be obtained when a mixture is made by combining 25 milliliters of tetrahydrofuran, 25 milliliters of methylene chloride, 2.5 grams of acrylonitrile-butadiene-stryrene copolymer (LUSTRAN
240-29), 2.5 grams of polyvinyl chloride (Alpha Plastics and Chemicals, clear rigid vinyl 2212/7-ll~), 1.2 grams of silver oxide powder, and 0.1 gram of gold chloride powder. The mixture may be stirred for about one hour.
Devices may be either dip coated or spray coated with this mixture. Upon evaporation of the solvents, an antimicrobial coating will remain on the device.
Equivalent results may be obtained when a mixture is made by combining 10 milliliters of alkoxy curing RTV, 65 milliliters of FREON TF solvent, 5 grams of silver oxide powder, and 0.5 gram of gold chloride powder. The mixture may be stirred for about one hour.
A silicone rubber Foley catheter or other silicone rubber medical device may be dipped into this mixture and upon evaporation of the solvent and curing of the RTV, a flexible, antimicrobial coating for the silicone rubber catheter is provided. Spray coating of the catheter is also an alternative application means.
Equivalent results may be obtained when a mixture is made by combining 100 milliliters of natural rubber latex with 10 grams of silver oxide powder. The mixture may be stirred until the silver oxide is dispersed.
Cured latex rubber devices may be dip coated with this ~2Z~7~7 mixture. Upon evaporation of the volatile liquid car-rier and curing of the coating mixture, an antimicrobial coating having high elastomeric characteristics will remain adhered to the device.
Equivalent results may be obtained when a mixture is made by combining 50 milliliters of methylene chlo-ride, 5 grams of acrylonitrile-butadiene-styrene copoly-mer (LUSTRAN 240-29), and 1.2 grams of copper oxide powder. The mixture may be stirred for about one hour.
A catheter adapter may be either dip coated or spray coated with this mixture. Upon evaporation of the solvent, an antimicrobial coating will remain bonded to the device.
Equivalent results may be obtained when a mixture is made by combining 50 milliliters of methylene chlo-ride, 5 grams of acrylonitrile-butadiene-styrene copoly-mer (LUSTRAN 240-29), and 1.2 grams of zinc oxide powder.
The mixture may be stirred for about one hour. A cathe-ter adapter may be either dip coated or spray coated with this mixture. Upon evaporation of the solvent, an antimicrobial coating will remain bonded to the de-vlce .
WHAT IS CLAIMED IS:
Claims (8)
1. An antimicrobial composition comprising:
30 to 85 percent by weight of a binder consisting essentially of a material selected from the group con-sisting of acrylonitrile-butadiene-styrene copolymers, polyvinyl chloride, mixtures thereof, polyesters, poly-urethanes, styrene-block copolymers, natural and syn-thetic rubbers, polycarbonates, nylon and silicone rubber; and, 15 to 70 percent by weight of an antimicrobial agent selected from the group consisting of compounds of physiological, antimicrobial metals and mixtures thereof.
30 to 85 percent by weight of a binder consisting essentially of a material selected from the group con-sisting of acrylonitrile-butadiene-styrene copolymers, polyvinyl chloride, mixtures thereof, polyesters, poly-urethanes, styrene-block copolymers, natural and syn-thetic rubbers, polycarbonates, nylon and silicone rubber; and, 15 to 70 percent by weight of an antimicrobial agent selected from the group consisting of compounds of physiological, antimicrobial metals and mixtures thereof.
2. The antimicrobial composition of Claim 1 in which said mixtures of acrylonitrile-butadiene-styrene copolymers and polyvinyl chloride consist of 25 to 75 percent by weight of acrylonitrile-butadiene-styrene copolymers and 25 to 75 percent by weight of polyvinyl chloride.
3. The antimicrobial composition of Claim 1 in which said antimicrobial agent is selected from the group consisting of oxides and salts of silver and gold.
4. The antimicrobial composition of Claim 1 in which said antimicrobial agent is selected from the group consisting of silver compounds.
5. The antimicrobial composition of Claim 4 in which said antimicrobial agent is silver oxide.
6. An antimicrobial composition for coating articles comprising:
30 to 85 percent by weight of a binder consisting essentially of acrylonitrile-butadiene-styrene copoly-mers; and, 15 to 70 percent by weight of an antimicrobial agent selected from the group consisting essentially of silver compounds and mixtures thereof whereby the particles of silver compound are exposed on the coating layer on the surface of the article and being sufficiently mobile to produce, within 24 hours, a solution of at least 10-6 molar concentration of silver ion concentration in a stagnant film of urine in contact with said surface.
30 to 85 percent by weight of a binder consisting essentially of acrylonitrile-butadiene-styrene copoly-mers; and, 15 to 70 percent by weight of an antimicrobial agent selected from the group consisting essentially of silver compounds and mixtures thereof whereby the particles of silver compound are exposed on the coating layer on the surface of the article and being sufficiently mobile to produce, within 24 hours, a solution of at least 10-6 molar concentration of silver ion concentration in a stagnant film of urine in contact with said surface.
7. An antimicrobial composition for coating articles comprising:
30 to 85 percent by weight of a binder consisting essentially of a mixture consisting of 35 to 65 percent by weight of acrylonitrile-butadiene-styrene copolymers and 35 to 65 percent by weight of polyvinyl chloride;
and, 15 to 70 percent by weight of an antimicrobial agent consisting essentially of silver oxide whereby the particles of silver oxide are exposed on the coating layer on the outermost surface of the article and being sufficiently mobile to produce, within 24 hours, a solution of at least 10-6 molar concentration of silver ion concentration in a stagnant film of urine in contact with said surface.
30 to 85 percent by weight of a binder consisting essentially of a mixture consisting of 35 to 65 percent by weight of acrylonitrile-butadiene-styrene copolymers and 35 to 65 percent by weight of polyvinyl chloride;
and, 15 to 70 percent by weight of an antimicrobial agent consisting essentially of silver oxide whereby the particles of silver oxide are exposed on the coating layer on the outermost surface of the article and being sufficiently mobile to produce, within 24 hours, a solution of at least 10-6 molar concentration of silver ion concentration in a stagnant film of urine in contact with said surface.
8. The antimicrobial composition of Claim 7 in which said mixtures of acrylonitrile-butadiene-styrene copolymers and polyvinyl chloride consist of 50 percent by weight of acrylonitrile-butadiene-styrene copolymers and 50 percent by weight of polyvinyl chloride.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
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US43950682A | 1982-11-05 | 1982-11-05 | |
US439,506 | 1982-11-05 |
Publications (1)
Publication Number | Publication Date |
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CA1224717A true CA1224717A (en) | 1987-07-28 |
Family
ID=23744984
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CA000439002A Expired CA1224717A (en) | 1982-11-05 | 1983-10-14 | Antimicrobial compositions |
Country Status (4)
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EP (1) | EP0124536A4 (en) |
CA (1) | CA1224717A (en) |
ES (1) | ES527051A0 (en) |
WO (1) | WO1984001721A1 (en) |
Families Citing this family (39)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4603152A (en) * | 1982-11-05 | 1986-07-29 | Baxter Travenol Laboratories, Inc. | Antimicrobial compositions |
WO1984004036A1 (en) * | 1983-04-18 | 1984-10-25 | Baxter Travenol Lab | Articles and compositions providing antimicrobial effect during urinary drainage |
EP0190504B1 (en) * | 1984-12-28 | 1993-04-21 | Johnson Matthey Public Limited Company | Antimicrobial compositions |
US4810247A (en) * | 1985-11-21 | 1989-03-07 | Glassman Jacob A | Urinary catheter and penile-cup |
DE3729253A1 (en) * | 1987-09-02 | 1989-03-23 | Ulrich Dr Mueller | Device for preventing infections in external fixators in bone surgery |
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-
1983
- 1983-09-15 WO PCT/US1983/001404 patent/WO1984001721A1/en not_active Application Discontinuation
- 1983-09-15 EP EP19830903140 patent/EP0124536A4/en not_active Withdrawn
- 1983-10-14 CA CA000439002A patent/CA1224717A/en not_active Expired
- 1983-11-05 ES ES527051A patent/ES527051A0/en active Granted
Also Published As
Publication number | Publication date |
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ES8504464A1 (en) | 1985-05-01 |
WO1984001721A1 (en) | 1984-05-10 |
EP0124536A4 (en) | 1985-06-06 |
EP0124536A1 (en) | 1984-11-14 |
ES527051A0 (en) | 1985-05-01 |
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