MXPA04009963A - Materiales de geles, articulos medicos y metodos de uso de los mismos. - Google Patents
Materiales de geles, articulos medicos y metodos de uso de los mismos.Info
- Publication number
- MXPA04009963A MXPA04009963A MXPA04009963A MXPA04009963A MXPA04009963A MX PA04009963 A MXPA04009963 A MX PA04009963A MX PA04009963 A MXPA04009963 A MX PA04009963A MX PA04009963 A MXPA04009963 A MX PA04009963A MX PA04009963 A MXPA04009963 A MX PA04009963A
- Authority
- MX
- Mexico
- Prior art keywords
- alkylene oxide
- group
- macromonomer
- poly
- multifunctional
- Prior art date
Links
- 239000000463 material Substances 0.000 title claims abstract description 118
- 238000000034 method Methods 0.000 title claims description 23
- 229920000233 poly(alkylene oxides) Polymers 0.000 claims abstract description 52
- 206010052428 Wound Diseases 0.000 claims description 117
- 208000027418 Wounds and injury Diseases 0.000 claims description 117
- 239000000178 monomer Substances 0.000 claims description 77
- 230000002745 absorbent Effects 0.000 claims description 64
- 239000002250 absorbent Substances 0.000 claims description 64
- 125000002947 alkylene group Chemical group 0.000 claims description 49
- 239000000203 mixture Substances 0.000 claims description 38
- 230000001070 adhesive effect Effects 0.000 claims description 36
- 239000000853 adhesive Substances 0.000 claims description 33
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 22
- 229920001577 copolymer Polymers 0.000 claims description 21
- 229920005604 random copolymer Polymers 0.000 claims description 21
- 230000002209 hydrophobic effect Effects 0.000 claims description 14
- 239000004820 Pressure-sensitive adhesive Substances 0.000 claims description 12
- 125000003118 aryl group Chemical group 0.000 claims description 10
- 239000000416 hydrocolloid Substances 0.000 claims description 10
- 150000003254 radicals Chemical class 0.000 claims description 9
- 125000002723 alicyclic group Chemical group 0.000 claims description 8
- 125000001931 aliphatic group Chemical group 0.000 claims description 8
- 229910052760 oxygen Inorganic materials 0.000 claims description 8
- 229920001519 homopolymer Polymers 0.000 claims description 7
- 239000013543 active substance Substances 0.000 claims description 5
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims description 4
- 230000001588 bifunctional effect Effects 0.000 claims description 4
- 239000008280 blood Substances 0.000 claims description 3
- 210000004369 blood Anatomy 0.000 claims description 3
- 230000029663 wound healing Effects 0.000 claims description 3
- 125000002877 alkyl aryl group Chemical group 0.000 claims description 2
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 2
- 239000003479 dental cement Substances 0.000 claims description 2
- 238000000465 moulding Methods 0.000 claims description 2
- 239000002245 particle Substances 0.000 claims description 2
- 239000002831 pharmacologic agent Substances 0.000 claims description 2
- 239000000565 sealant Substances 0.000 claims description 2
- 125000004185 ester group Chemical group 0.000 claims 1
- 230000002538 fungal effect Effects 0.000 claims 1
- 238000006116 polymerization reaction Methods 0.000 abstract description 8
- 239000010410 layer Substances 0.000 description 140
- 239000000499 gel Substances 0.000 description 100
- 229920000642 polymer Polymers 0.000 description 64
- 229920001223 polyethylene glycol Polymers 0.000 description 36
- -1 acrylamido Chemical group 0.000 description 26
- 210000000416 exudates and transudate Anatomy 0.000 description 25
- 239000007788 liquid Substances 0.000 description 22
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 22
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 21
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 19
- 230000015572 biosynthetic process Effects 0.000 description 19
- 239000012530 fluid Substances 0.000 description 16
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 16
- 239000000243 solution Substances 0.000 description 16
- 239000000126 substance Substances 0.000 description 16
- 239000000047 product Substances 0.000 description 15
- 239000011780 sodium chloride Substances 0.000 description 13
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 12
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 11
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 10
- 239000005977 Ethylene Substances 0.000 description 10
- 238000002360 preparation method Methods 0.000 description 9
- 230000008961 swelling Effects 0.000 description 9
- 239000006188 syrup Substances 0.000 description 9
- 235000020357 syrup Nutrition 0.000 description 9
- 210000001124 body fluid Anatomy 0.000 description 8
- 229920000728 polyester Polymers 0.000 description 8
- 238000003756 stirring Methods 0.000 description 8
- GJKGAPPUXSSCFI-UHFFFAOYSA-N 2-Hydroxy-4'-(2-hydroxyethoxy)-2-methylpropiophenone Chemical compound CC(C)(O)C(=O)C1=CC=C(OCCO)C=C1 GJKGAPPUXSSCFI-UHFFFAOYSA-N 0.000 description 7
- 239000005058 Isophorone diisocyanate Substances 0.000 description 7
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 7
- 239000012790 adhesive layer Substances 0.000 description 7
- XYLMUPLGERFSHI-UHFFFAOYSA-N alpha-Methylstyrene Chemical compound CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 description 7
- 230000005540 biological transmission Effects 0.000 description 7
- 238000005227 gel permeation chromatography Methods 0.000 description 7
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 7
- 239000004814 polyurethane Substances 0.000 description 7
- 229920002635 polyurethane Polymers 0.000 description 7
- WOBHKFSMXKNTIM-UHFFFAOYSA-N Hydroxyethyl methacrylate Chemical compound CC(=C)C(=O)OCCO WOBHKFSMXKNTIM-UHFFFAOYSA-N 0.000 description 6
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 6
- 238000010521 absorption reaction Methods 0.000 description 6
- 239000010839 body fluid Substances 0.000 description 6
- 239000003054 catalyst Substances 0.000 description 6
- NIMLQBUJDJZYEJ-UHFFFAOYSA-N isophorone diisocyanate Chemical compound CC1(C)CC(N=C=O)CC(C)(CN=C=O)C1 NIMLQBUJDJZYEJ-UHFFFAOYSA-N 0.000 description 6
- 229910052757 nitrogen Inorganic materials 0.000 description 6
- 238000003786 synthesis reaction Methods 0.000 description 6
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 5
- DXPPIEDUBFUSEZ-UHFFFAOYSA-N 6-methylheptyl prop-2-enoate Chemical compound CC(C)CCCCCOC(=O)C=C DXPPIEDUBFUSEZ-UHFFFAOYSA-N 0.000 description 5
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 5
- 241001465754 Metazoa Species 0.000 description 5
- 229920002614 Polyether block amide Polymers 0.000 description 5
- 229920000297 Rayon Polymers 0.000 description 5
- 238000006243 chemical reaction Methods 0.000 description 5
- 239000003795 chemical substances by application Substances 0.000 description 5
- HJOVHMDZYOCNQW-UHFFFAOYSA-N isophorone Chemical compound CC1=CC(=O)CC(C)(C)C1 HJOVHMDZYOCNQW-UHFFFAOYSA-N 0.000 description 5
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 4
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 4
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 4
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 description 4
- 206010039509 Scab Diseases 0.000 description 4
- 239000002253 acid Substances 0.000 description 4
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- 238000010276 construction Methods 0.000 description 4
- 239000001301 oxygen Substances 0.000 description 4
- 229920001281 polyalkylene Polymers 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- 210000001519 tissue Anatomy 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 description 3
- NLZUEZXRPGMBCV-UHFFFAOYSA-N Butylhydroxytoluene Chemical compound CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 NLZUEZXRPGMBCV-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 3
- 239000004698 Polyethylene Substances 0.000 description 3
- 239000004743 Polypropylene Substances 0.000 description 3
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 3
- 229910021607 Silver chloride Inorganic materials 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- UKLDJPRMSDWDSL-UHFFFAOYSA-L [dibutyl(dodecanoyloxy)stannyl] dodecanoate Chemical compound CCCCCCCCCCCC(=O)O[Sn](CCCC)(CCCC)OC(=O)CCCCCCCCCCC UKLDJPRMSDWDSL-UHFFFAOYSA-L 0.000 description 3
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 3
- 239000000654 additive Substances 0.000 description 3
- 125000000217 alkyl group Chemical group 0.000 description 3
- 239000003242 anti bacterial agent Substances 0.000 description 3
- 230000004888 barrier function Effects 0.000 description 3
- 229920001400 block copolymer Polymers 0.000 description 3
- 235000010354 butylated hydroxytoluene Nutrition 0.000 description 3
- 239000007795 chemical reaction product Substances 0.000 description 3
- 239000012975 dibutyltin dilaurate Substances 0.000 description 3
- 125000005442 diisocyanate group Chemical group 0.000 description 3
- 238000009826 distribution Methods 0.000 description 3
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 3
- 230000035876 healing Effects 0.000 description 3
- 230000036571 hydration Effects 0.000 description 3
- 238000006703 hydration reaction Methods 0.000 description 3
- 239000003999 initiator Substances 0.000 description 3
- DCUFMVPCXCSVNP-UHFFFAOYSA-N methacrylic anhydride Chemical compound CC(=C)C(=O)OC(=O)C(C)=C DCUFMVPCXCSVNP-UHFFFAOYSA-N 0.000 description 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 3
- 239000004014 plasticizer Substances 0.000 description 3
- 229920000573 polyethylene Polymers 0.000 description 3
- 239000003505 polymerization initiator Substances 0.000 description 3
- 229920001155 polypropylene Polymers 0.000 description 3
- 229920001296 polysiloxane Polymers 0.000 description 3
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 3
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 3
- 229940009188 silver Drugs 0.000 description 3
- 229910052709 silver Inorganic materials 0.000 description 3
- 239000004332 silver Substances 0.000 description 3
- HKZLPVFGJNLROG-UHFFFAOYSA-M silver monochloride Chemical compound [Cl-].[Ag+] HKZLPVFGJNLROG-UHFFFAOYSA-M 0.000 description 3
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 3
- 238000012546 transfer Methods 0.000 description 3
- 238000002834 transmittance Methods 0.000 description 3
- 230000000472 traumatic effect Effects 0.000 description 3
- GQHTUMJGOHRCHB-UHFFFAOYSA-N 2,3,4,6,7,8,9,10-octahydropyrimido[1,2-a]azepine Chemical compound C1CCCCN2CCCN=C21 GQHTUMJGOHRCHB-UHFFFAOYSA-N 0.000 description 2
- OZAIFHULBGXAKX-UHFFFAOYSA-N 2-(2-cyanopropan-2-yldiazenyl)-2-methylpropanenitrile Chemical compound N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 description 2
- JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical class FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 description 2
- LWRBVKNFOYUCNP-UHFFFAOYSA-N 2-methyl-1-(4-methylsulfanylphenyl)-2-morpholin-4-ylpropan-1-one Chemical compound C1=CC(SC)=CC=C1C(=O)C(C)(C)N1CCOCC1 LWRBVKNFOYUCNP-UHFFFAOYSA-N 0.000 description 2
- IUNVCWLKOOCPIT-UHFFFAOYSA-N 6-methylheptylsulfanyl 2-hydroxyacetate Chemical compound CC(C)CCCCCSOC(=O)CO IUNVCWLKOOCPIT-UHFFFAOYSA-N 0.000 description 2
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 2
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- GHXZTYHSJHQHIJ-UHFFFAOYSA-N Chlorhexidine Chemical compound C=1C=C(Cl)C=CC=1NC(N)=NC(N)=NCCCCCCN=C(N)N=C(N)NC1=CC=C(Cl)C=C1 GHXZTYHSJHQHIJ-UHFFFAOYSA-N 0.000 description 2
- 241000196324 Embryophyta Species 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- 238000005481 NMR spectroscopy Methods 0.000 description 2
- 239000004952 Polyamide Substances 0.000 description 2
- 208000004210 Pressure Ulcer Diseases 0.000 description 2
- 239000006096 absorbing agent Substances 0.000 description 2
- 125000003647 acryloyl group Chemical group O=C([*])C([H])=C([H])[H] 0.000 description 2
- 125000002102 aryl alkyloxo group Chemical group 0.000 description 2
- 230000003385 bacteriostatic effect Effects 0.000 description 2
- BLFLLBZGZJTVJG-UHFFFAOYSA-N benzocaine Chemical compound CCOC(=O)C1=CC=C(N)C=C1 BLFLLBZGZJTVJG-UHFFFAOYSA-N 0.000 description 2
- YKPUWZUDDOIDPM-SOFGYWHQSA-N capsaicin Chemical compound COC1=CC(CNC(=O)CCCC\C=C\C(C)C)=CC=C1O YKPUWZUDDOIDPM-SOFGYWHQSA-N 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 125000002057 carboxymethyl group Chemical group [H]OC(=O)C([H])([H])[*] 0.000 description 2
- 229960003260 chlorhexidine Drugs 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 238000011109 contamination Methods 0.000 description 2
- WNAHIZMDSQCWRP-UHFFFAOYSA-N dodecane-1-thiol Chemical compound CCCCCCCCCCCCS WNAHIZMDSQCWRP-UHFFFAOYSA-N 0.000 description 2
- 229940079593 drug Drugs 0.000 description 2
- 239000003814 drug Substances 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- HNRMPXKDFBEGFZ-UHFFFAOYSA-N ethyl trimethyl methane Natural products CCC(C)(C)C HNRMPXKDFBEGFZ-UHFFFAOYSA-N 0.000 description 2
- 238000010528 free radical solution polymerization reaction Methods 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
- CGIGDMFJXJATDK-UHFFFAOYSA-N indomethacin Chemical compound CC1=C(CC(O)=O)C2=CC(OC)=CC=C2N1C(=O)C1=CC=C(Cl)C=C1 CGIGDMFJXJATDK-UHFFFAOYSA-N 0.000 description 2
- 208000015181 infectious disease Diseases 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Chemical class OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 2
- 235000019645 odor Nutrition 0.000 description 2
- 230000035699 permeability Effects 0.000 description 2
- 239000003208 petroleum Substances 0.000 description 2
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 2
- 229920002647 polyamide Polymers 0.000 description 2
- 229920006267 polyester film Polymers 0.000 description 2
- 229920002959 polymer blend Polymers 0.000 description 2
- 229920006254 polymer film Polymers 0.000 description 2
- 229920001451 polypropylene glycol Polymers 0.000 description 2
- 229920006264 polyurethane film Polymers 0.000 description 2
- 229920000915 polyvinyl chloride Polymers 0.000 description 2
- 229940069328 povidone Drugs 0.000 description 2
- 230000005855 radiation Effects 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- NDVLTYZPCACLMA-UHFFFAOYSA-N silver oxide Chemical compound [O-2].[Ag+].[Ag+] NDVLTYZPCACLMA-UHFFFAOYSA-N 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 239000002562 thickening agent Substances 0.000 description 2
- 238000004809 thin layer chromatography Methods 0.000 description 2
- DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical compound CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 description 2
- 125000005628 tolylene group Chemical group 0.000 description 2
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 2
- 229920002554 vinyl polymer Polymers 0.000 description 2
- 238000011179 visual inspection Methods 0.000 description 2
- NOOLISFMXDJSKH-UTLUCORTSA-N (+)-Neomenthol Chemical compound CC(C)[C@@H]1CC[C@@H](C)C[C@@H]1O NOOLISFMXDJSKH-UTLUCORTSA-N 0.000 description 1
- QNODIIQQMGDSEF-UHFFFAOYSA-N (1-hydroxycyclohexyl)-phenylmethanone Chemical compound C=1C=CC=CC=1C(=O)C1(O)CCCCC1 QNODIIQQMGDSEF-UHFFFAOYSA-N 0.000 description 1
- XMAYWYJOQHXEEK-OZXSUGGESA-N (2R,4S)-ketoconazole Chemical compound C1CN(C(=O)C)CCN1C(C=C1)=CC=C1OC[C@@H]1O[C@@](CN2C=NC=C2)(C=2C(=CC(Cl)=CC=2)Cl)OC1 XMAYWYJOQHXEEK-OZXSUGGESA-N 0.000 description 1
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 description 1
- DSSYKIVIOFKYAU-XCBNKYQSSA-N (R)-camphor Chemical compound C1C[C@@]2(C)C(=O)C[C@@H]1C2(C)C DSSYKIVIOFKYAU-XCBNKYQSSA-N 0.000 description 1
- MCCACAIVAXEFAL-UHFFFAOYSA-N 1-[2-(2,4-dichlorophenyl)-2-[(2,4-dichlorophenyl)methoxy]ethyl]imidazole;nitric acid Chemical compound O[N+]([O-])=O.ClC1=CC(Cl)=CC=C1COC(C=1C(=CC(Cl)=CC=1)Cl)CN1C=NC=C1 MCCACAIVAXEFAL-UHFFFAOYSA-N 0.000 description 1
- JWYVGKFDLWWQJX-UHFFFAOYSA-N 1-ethenylazepan-2-one Chemical compound C=CN1CCCCCC1=O JWYVGKFDLWWQJX-UHFFFAOYSA-N 0.000 description 1
- 239000012956 1-hydroxycyclohexylphenyl-ketone Substances 0.000 description 1
- KWVGIHKZDCUPEU-UHFFFAOYSA-N 2,2-dimethoxy-2-phenylacetophenone Chemical compound C=1C=CC=CC=1C(OC)(OC)C(=O)C1=CC=CC=C1 KWVGIHKZDCUPEU-UHFFFAOYSA-N 0.000 description 1
- PYMYPHUHKUWMLA-UHFFFAOYSA-N 2,3,4,5-tetrahydroxypentanal Chemical compound OCC(O)C(O)C(O)C=O PYMYPHUHKUWMLA-UHFFFAOYSA-N 0.000 description 1
- QRIMLDXJAPZHJE-UHFFFAOYSA-N 2,3-dihydroxypropyl 2-methylprop-2-enoate Chemical class CC(=C)C(=O)OCC(O)CO QRIMLDXJAPZHJE-UHFFFAOYSA-N 0.000 description 1
- IEJPPSMHUUQABK-UHFFFAOYSA-N 2,4-diphenyl-4h-1,3-oxazol-5-one Chemical compound O=C1OC(C=2C=CC=CC=2)=NC1C1=CC=CC=C1 IEJPPSMHUUQABK-UHFFFAOYSA-N 0.000 description 1
- VBZBISQOWJYWCC-UHFFFAOYSA-N 2-(2-carboxypropan-2-yldiazenyl)-2-methylpropanoic acid Chemical compound OC(=O)C(C)(C)N=NC(C)(C)C(O)=O VBZBISQOWJYWCC-UHFFFAOYSA-N 0.000 description 1
- WYGWHHGCAGTUCH-UHFFFAOYSA-N 2-[(2-cyano-4-methylpentan-2-yl)diazenyl]-2,4-dimethylpentanenitrile Chemical compound CC(C)CC(C)(C#N)N=NC(C)(C#N)CC(C)C WYGWHHGCAGTUCH-UHFFFAOYSA-N 0.000 description 1
- TXBCBTDQIULDIA-UHFFFAOYSA-N 2-[[3-hydroxy-2,2-bis(hydroxymethyl)propoxy]methyl]-2-(hydroxymethyl)propane-1,3-diol Chemical compound OCC(CO)(CO)COCC(CO)(CO)CO TXBCBTDQIULDIA-UHFFFAOYSA-N 0.000 description 1
- UHFFVFAKEGKNAQ-UHFFFAOYSA-N 2-benzyl-2-(dimethylamino)-1-(4-morpholin-4-ylphenyl)butan-1-one Chemical compound C=1C=C(N2CCOCC2)C=CC=1C(=O)C(CC)(N(C)C)CC1=CC=CC=C1 UHFFVFAKEGKNAQ-UHFFFAOYSA-N 0.000 description 1
- MPNXSZJPSVBLHP-UHFFFAOYSA-N 2-chloro-n-phenylpyridine-3-carboxamide Chemical compound ClC1=NC=CC=C1C(=O)NC1=CC=CC=C1 MPNXSZJPSVBLHP-UHFFFAOYSA-N 0.000 description 1
- WROUWQQRXUBECT-UHFFFAOYSA-M 2-ethylacrylate Chemical compound CCC(=C)C([O-])=O WROUWQQRXUBECT-UHFFFAOYSA-M 0.000 description 1
- XMLYCEVDHLAQEL-UHFFFAOYSA-N 2-hydroxy-2-methyl-1-phenylpropan-1-one Chemical compound CC(C)(O)C(=O)C1=CC=CC=C1 XMLYCEVDHLAQEL-UHFFFAOYSA-N 0.000 description 1
- RIWRBSMFKVOJMN-UHFFFAOYSA-N 2-methyl-1-phenylpropan-2-ol Chemical compound CC(C)(O)CC1=CC=CC=C1 RIWRBSMFKVOJMN-UHFFFAOYSA-N 0.000 description 1
- IKEHOXWJQXIQAG-UHFFFAOYSA-N 2-tert-butyl-4-methylphenol Chemical compound CC1=CC=C(O)C(C(C)(C)C)=C1 IKEHOXWJQXIQAG-UHFFFAOYSA-N 0.000 description 1
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- 229920001169 thermoplastic Polymers 0.000 description 1
- 229920002725 thermoplastic elastomer Polymers 0.000 description 1
- FUSNMLFNXJSCDI-UHFFFAOYSA-N tolnaftate Chemical compound C=1C=C2C=CC=CC2=CC=1OC(=S)N(C)C1=CC=CC(C)=C1 FUSNMLFNXJSCDI-UHFFFAOYSA-N 0.000 description 1
- 229960004880 tolnaftate Drugs 0.000 description 1
- 230000007704 transition Effects 0.000 description 1
- 229960003500 triclosan Drugs 0.000 description 1
- IEDVJHCEMCRBQM-UHFFFAOYSA-N trimethoprim Chemical compound COC1=C(OC)C(OC)=CC(CC=2C(=NC(N)=NC=2)N)=C1 IEDVJHCEMCRBQM-UHFFFAOYSA-N 0.000 description 1
- 229960001082 trimethoprim Drugs 0.000 description 1
- 231100000397 ulcer Toxicity 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N urea group Chemical group NC(=O)N XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- 150000003673 urethanes Chemical class 0.000 description 1
- 239000004034 viscosity adjusting agent Substances 0.000 description 1
- 239000011782 vitamin Substances 0.000 description 1
- 235000013343 vitamin Nutrition 0.000 description 1
- 229940088594 vitamin Drugs 0.000 description 1
- 229930003231 vitamin Natural products 0.000 description 1
- 239000011800 void material Substances 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 239000003643 water by type Substances 0.000 description 1
- 229920001285 xanthan gum Polymers 0.000 description 1
- 235000010493 xanthan gum Nutrition 0.000 description 1
- 239000000230 xanthan gum Substances 0.000 description 1
- 229940082509 xanthan gum Drugs 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- 239000010457 zeolite Substances 0.000 description 1
- UHVMMEOXYDMDKI-JKYCWFKZSA-L zinc;1-(5-cyanopyridin-2-yl)-3-[(1s,2s)-2-(6-fluoro-2-hydroxy-3-propanoylphenyl)cyclopropyl]urea;diacetate Chemical compound [Zn+2].CC([O-])=O.CC([O-])=O.CCC(=O)C1=CC=C(F)C([C@H]2[C@H](C2)NC(=O)NC=2N=CC(=CC=2)C#N)=C1O UHVMMEOXYDMDKI-JKYCWFKZSA-L 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F290/00—Macromolecular compounds obtained by polymerising monomers on to polymers modified by introduction of aliphatic unsaturated end or side groups
- C08F290/08—Macromolecular compounds obtained by polymerising monomers on to polymers modified by introduction of aliphatic unsaturated end or side groups on to polymers modified by introduction of unsaturated side groups
- C08F290/14—Polymers provided for in subclass C08G
- C08F290/142—Polyethers
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K6/00—Preparations for dentistry
- A61K6/90—Compositions for taking dental impressions
-
- 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
- A61L15/00—Chemical aspects of, or use of materials for, bandages, dressings or absorbent pads
- A61L15/16—Bandages, dressings or absorbent pads for physiological fluids such as urine or blood, e.g. sanitary towels, tampons
- A61L15/42—Use of materials characterised by their function or physical properties
- A61L15/60—Liquid-swellable gel-forming materials, e.g. super-absorbents
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F290/00—Macromolecular compounds obtained by polymerising monomers on to polymers modified by introduction of aliphatic unsaturated end or side groups
- C08F290/02—Macromolecular compounds obtained by polymerising monomers on to polymers modified by introduction of aliphatic unsaturated end or side groups on to polymers modified by introduction of unsaturated end groups
- C08F290/06—Polymers provided for in subclass C08G
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F290/00—Macromolecular compounds obtained by polymerising monomers on to polymers modified by introduction of aliphatic unsaturated end or side groups
- C08F290/02—Macromolecular compounds obtained by polymerising monomers on to polymers modified by introduction of aliphatic unsaturated end or side groups on to polymers modified by introduction of unsaturated end groups
- C08F290/06—Polymers provided for in subclass C08G
- C08F290/062—Polyethers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F290/00—Macromolecular compounds obtained by polymerising monomers on to polymers modified by introduction of aliphatic unsaturated end or side groups
- C08F290/08—Macromolecular compounds obtained by polymerising monomers on to polymers modified by introduction of aliphatic unsaturated end or side groups on to polymers modified by introduction of unsaturated side groups
- C08F290/14—Polymers provided for in subclass C08G
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Epidemiology (AREA)
- Animal Behavior & Ethology (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Oral & Maxillofacial Surgery (AREA)
- Dispersion Chemistry (AREA)
- Materials Engineering (AREA)
- Engineering & Computer Science (AREA)
- Hematology (AREA)
- Macromonomer-Based Addition Polymer (AREA)
- Materials For Medical Uses (AREA)
- Medicines Containing Material From Animals Or Micro-Organisms (AREA)
- Prostheses (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US10/121,518 US7005143B2 (en) | 2002-04-12 | 2002-04-12 | Gel materials, medical articles, and methods |
| PCT/US2003/009556 WO2003086493A1 (en) | 2002-04-12 | 2003-03-27 | Gel materials, medical articles, and methods |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MXPA04009963A true MXPA04009963A (es) | 2004-12-13 |
Family
ID=29248305
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MXPA04009963A MXPA04009963A (es) | 2002-04-12 | 2003-03-27 | Materiales de geles, articulos medicos y metodos de uso de los mismos. |
Country Status (13)
| Country | Link |
|---|---|
| US (2) | US7005143B2 (https=) |
| EP (2) | EP1494727B1 (https=) |
| JP (1) | JP4550428B2 (https=) |
| KR (1) | KR100982415B1 (https=) |
| CN (1) | CN1327908C (https=) |
| AT (1) | ATE381355T1 (https=) |
| AU (1) | AU2003228392A1 (https=) |
| BR (1) | BRPI0309109B8 (https=) |
| CA (1) | CA2481765C (https=) |
| DE (1) | DE60318189T2 (https=) |
| ES (1) | ES2297161T3 (https=) |
| MX (1) | MXPA04009963A (https=) |
| WO (1) | WO2003086493A1 (https=) |
Families Citing this family (98)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ATE376083T1 (de) * | 2002-12-10 | 2007-11-15 | Dsm Ip Assets Bv | Verfahren zur herstellung und verfahren zur konvertierung von polyolefinfasern |
| EP1587502B2 (en) * | 2002-12-31 | 2025-05-21 | BSN medical GmbH | Wound dressing |
| US20050070688A1 (en) * | 2003-09-26 | 2005-03-31 | 3M Innovative Properties Company | Reactive hydrophilic oligomers |
| US20050074407A1 (en) * | 2003-10-01 | 2005-04-07 | Sonotech, Inc. | PVP and PVA as in vivo biocompatible acoustic coupling medium |
| US7384984B2 (en) * | 2003-12-10 | 2008-06-10 | 3M Innovative Properties Company | Reactive hydrophilic oligomers |
| US7074839B2 (en) * | 2004-03-01 | 2006-07-11 | 3M Innovative Properties Company | Crosslinkable hydrophilic materials from reactive oligomers having pendent photoinitiator groups |
| US7342047B2 (en) * | 2004-03-02 | 2008-03-11 | 3M Innovative Properties Company | Crosslinkable hydrophilic materials from reactive oligomers having pendent unsaturated groups |
| EP1616583B1 (de) * | 2004-07-16 | 2008-06-25 | Collano AG | Heissschmelzzusammensetzung mit Hydrocolloid |
| ES2300048T3 (es) * | 2004-08-25 | 2008-06-01 | UNION CARBIDE CHEMICALS & PLASTICS TECHNOLOGY CORPORATION | Pelicula polimerica. |
| DE102004042799A1 (de) * | 2004-09-03 | 2006-03-09 | Basf Ag | Verfahren zur Herstellung von Poly-(C2-C4-alkylenglykol)-mono(meth)acrylsäureestern |
| US7999023B2 (en) * | 2004-12-03 | 2011-08-16 | 3M Innovative Properties Company | Process for making pressure sensitive adhesive hydrogels |
| US20060127316A1 (en) * | 2004-12-14 | 2006-06-15 | Sonotech, Inc. | Polyols and PVP as in vivo biocompatible acoustic coupling media |
| US8609131B2 (en) * | 2005-01-25 | 2013-12-17 | 3M Innovative Properties Company | Absorbent dressing comprising hydrophilic polymer prepared via Michael reaction |
| US7749531B2 (en) | 2005-06-08 | 2010-07-06 | Indicator Systems International | Apparatus and method for detecting bacterial growth beneath a wound dressing |
| AU2006270308A1 (en) * | 2005-07-15 | 2007-01-25 | Covidien Lp | Wound dressing and methods of making and using the same |
| US20070083175A1 (en) * | 2005-10-11 | 2007-04-12 | Kimberly-Clark Worldwide, Inc. | Transparent/translucent absorbent composites and articles |
| KR100748390B1 (ko) * | 2005-11-14 | 2007-08-10 | 주식회사 대웅 | 상피세포성장인자를 포함하는 상처치료용 서방성 필름 제형 |
| US7619131B2 (en) | 2005-12-02 | 2009-11-17 | Kimberly-Clark Worldwide, Inc. | Articles comprising transparent/translucent polymer composition |
| US7981949B2 (en) | 2006-05-23 | 2011-07-19 | 3M Innovative Properties Company | Curable hydrophilic compositions |
| US7659344B2 (en) * | 2006-06-08 | 2010-02-09 | E. I. Du Pont De Nemours And Company | Shaped articles containing poly(vinylpyrrolidone)-iodine complex |
| JP5256590B2 (ja) * | 2006-08-04 | 2013-08-07 | 東亞合成株式会社 | 重合体微粒子の製造方法 |
| EP2081528B1 (en) * | 2006-09-26 | 2018-11-14 | T.J. Smith & Nephew, Limited | Lattice dressing |
| US9820888B2 (en) | 2006-09-26 | 2017-11-21 | Smith & Nephew, Inc. | Wound dressing |
| DE602007004546D1 (de) | 2006-09-28 | 2010-03-18 | Tyco Healthcare | Tragbares Wundtherapiesystem |
| CA2664242A1 (en) | 2006-10-05 | 2008-04-10 | Basf Se | Comb polymers and use thereof for the production of active or effective ingredient formulations |
| AU2007331453A1 (en) | 2006-12-15 | 2008-06-19 | Coloplast A/S | Coatings prepared from poly(ethylene oxide) and photo-initator-containing scaffolds |
| BRPI0718328A2 (pt) | 2006-12-15 | 2011-10-11 | Lifebond Ltd | composição, curativo hemostático e dispositivo médico para a inserção em um corpo de um ser humano ou de um mamìfero inferior |
| BRPI0720268B8 (pt) | 2006-12-15 | 2021-06-22 | Coloplast As | método para a preparação de um elemento de dispositivo médico, e, dispositivo médico |
| US7939578B2 (en) * | 2007-02-23 | 2011-05-10 | 3M Innovative Properties Company | Polymeric fibers and methods of making |
| US8513322B2 (en) * | 2007-05-31 | 2013-08-20 | 3M Innovative Properties Company | Polymeric beads and methods of making polymeric beads |
| US8734413B2 (en) | 2007-08-03 | 2014-05-27 | Kimberly-Clark Worldwide, Inc. | Packaged body adhering absorbent article |
| US8672911B2 (en) | 2007-08-03 | 2014-03-18 | Kimberly-Clark Worldwide, Inc. | Body adhering absorbent article |
| US7947027B2 (en) | 2007-12-28 | 2011-05-24 | Kimberly-Clark Worldwide, Inc. | Body adhering absorbent article |
| US8292862B2 (en) | 2007-08-03 | 2012-10-23 | Kimberly-Clark Worldwide, Inc. | Dynamic fitting body adhering absorbent article |
| US20090098073A1 (en) * | 2007-10-12 | 2009-04-16 | Macdonald John Gavin | Phase change visual indicating composition |
| WO2009061831A1 (en) * | 2007-11-08 | 2009-05-14 | Indicator Systems International, Inc. | Polymeric indicators for detecting the presence of metabolic byproducts from microorganisms |
| BRPI0820704A2 (pt) | 2007-12-12 | 2015-06-16 | 3M Innovative Proferties Company | Métodos de fabricação de materiais poliméricos moldados |
| US20100266794A1 (en) | 2007-12-12 | 2010-10-21 | Wright Robin E | Hydrophilic gel materials and methods of making |
| US9033942B2 (en) * | 2008-03-07 | 2015-05-19 | Smith & Nephew, Inc. | Wound dressing port and associated wound dressing |
| US8298200B2 (en) | 2009-06-01 | 2012-10-30 | Tyco Healthcare Group Lp | System for providing continual drainage in negative pressure wound therapy |
| BRPI0906527A2 (pt) * | 2008-04-04 | 2016-09-06 | 3Mm Innovative Properties Company | aparelho para aplicação de bandagens em ferimentos e bandagem médica |
| CN102065848A (zh) * | 2008-04-21 | 2011-05-18 | 3M创新有限公司 | 释放一氧化一氮的组合物、装置和方法 |
| EP2487206A3 (en) | 2008-06-18 | 2012-11-28 | Lifebond Ltd | Cross-linkable gelatin-based compositions |
| WO2009154568A1 (en) * | 2008-06-20 | 2009-12-23 | Agency For Science, Technology And Research | Water swellable and water soluble polymers and use thereof |
| DE102008040214A1 (de) * | 2008-07-07 | 2010-01-14 | Evonik Röhm Gmbh | Verfahren zur Herstellung von Polyalkylenglykoldi(meth)acrylaten |
| US8846595B2 (en) * | 2008-07-14 | 2014-09-30 | 3M Innovative Properties Company | Method of making a cleaning solution from hydrogel cleaning concentrate and packaged cleaning concentrate |
| US11147722B2 (en) | 2008-11-10 | 2021-10-19 | Kimberly-Clark Worldwide, Inc. | Absorbent article with a multifunctional acrylate skin-adhesive composition |
| EP2379226B1 (en) | 2008-12-31 | 2016-04-20 | 3M Innovative Properties Company | Live bioload detection using microparticles |
| EP2379697A2 (en) | 2008-12-31 | 2011-10-26 | 3M Innovative Properties Company | Sampling devices and methods for concentrating microorganisms |
| EP2382080A4 (en) * | 2009-01-26 | 2014-12-17 | Indicator Systems International Inc | INDICATORS FOR INDICATING THE PRESENCE OF MICRO-ORGANISM INFLUENCING PRODUCTS |
| EP2391322A1 (de) * | 2009-02-02 | 2011-12-07 | BSN medical GmbH | Wundauflage, Verfahren zu ihrer Herstellung und ihre Verwendung zur Wundversorgung |
| US10022468B2 (en) * | 2009-02-02 | 2018-07-17 | Kimberly-Clark Worldwide, Inc. | Absorbent articles containing a multifunctional gel |
| US20100324516A1 (en) | 2009-06-18 | 2010-12-23 | Tyco Healthcare Group Lp | Apparatus for Vacuum Bridging and/or Exudate Collection |
| US8690844B2 (en) * | 2009-08-27 | 2014-04-08 | Kci Licensing, Inc. | Re-epithelialization wound dressings and systems |
| US20110054420A1 (en) * | 2009-08-27 | 2011-03-03 | Christopher Brian Locke | Reduced-pressure wound dressings and systems for re-epithelialization and granulation |
| DE102009049506A1 (de) * | 2009-10-15 | 2011-04-21 | Schülke & Mayr GmbH | Octenidindihydrochlorid enthaltende Wundauflage zur Anwendung bei der Antiseptik von Kathetereintrittsstellen |
| DK2515961T3 (da) | 2009-12-22 | 2019-07-15 | Smith & Nephew Inc | Apparatuses and methods for negative pressure wound therapy |
| WO2011077388A1 (en) | 2009-12-22 | 2011-06-30 | Lifebond Ltd | Modification of enzymatic crosslinkers for controlling properties of crosslinked matrices |
| EP2519355B1 (en) | 2009-12-30 | 2017-01-25 | 3M Innovative Properties Company | Live bioload detection using microparticles |
| US8845801B2 (en) | 2009-12-30 | 2014-09-30 | Regents Of The University Of Minnesota | Bone cement and method |
| US9061095B2 (en) | 2010-04-27 | 2015-06-23 | Smith & Nephew Plc | Wound dressing and method of use |
| USRE48117E1 (en) | 2010-05-07 | 2020-07-28 | Smith & Nephew, Inc. | Apparatuses and methods for negative pressure wound therapy |
| US8961544B2 (en) | 2010-08-05 | 2015-02-24 | Lifebond Ltd. | Dry composition wound dressings and adhesives comprising gelatin and transglutaminase in a cross-linked matrix |
| USD714433S1 (en) | 2010-12-22 | 2014-09-30 | Smith & Nephew, Inc. | Suction adapter |
| EP2654821B1 (en) | 2010-12-22 | 2019-05-08 | Smith & Nephew, Inc. | Apparatuses for negative pressure wound therapy |
| CN102599758A (zh) * | 2011-01-28 | 2012-07-25 | 上海英科医疗用品有限公司 | 一种凝胶床垫的胶体溶液及其生产方法 |
| US9309443B2 (en) | 2012-05-29 | 2016-04-12 | 3M Innovative Properties Company | Liquid optical adhesive compositions |
| KR20150095746A (ko) | 2012-12-10 | 2015-08-21 | 쓰리엠 이노베이티브 프로퍼티즈 컴파니 | 액체 광학 접착제 조성물 |
| CN105745237B (zh) | 2013-11-21 | 2018-06-05 | 3M创新有限公司 | 液体光学粘合剂组合物 |
| EP3071613A1 (en) | 2013-11-21 | 2016-09-28 | 3M Innovative Properties Company | Liquid optical adhesive compositions |
| US9259514B2 (en) * | 2013-12-18 | 2016-02-16 | Ethicon, Inc. | Absorbable polymeric blend compositions based on copolymers prepared from mono- and di-functional polymerization initiators, processing methods, and medical devices therefrom |
| WO2016053875A1 (en) | 2014-10-01 | 2016-04-07 | 3M Innovative Properties Company | Medical dressings comprising fluid management articles and methods of using same |
| WO2016100089A1 (en) | 2014-12-19 | 2016-06-23 | 3M Innovative Properties Company | Viscoelastic wound closure dressing |
| EP3240580B1 (en) * | 2014-12-30 | 2020-04-15 | 3M Innovative Properties Company | Negative pressure wound dressing with absorbent adhesive sealant layer |
| US20170173209A1 (en) * | 2015-12-18 | 2017-06-22 | Rousseau Research, Inc. | Wound closure compositions and method |
| GB201703383D0 (en) | 2017-03-02 | 2017-04-19 | Gargle Tech Ltd | Testing for particulates |
| AU2018281120A1 (en) | 2017-06-07 | 2020-01-02 | 3M Innovative Properties Company | Peel and place dressing for negative-pressure treatment |
| WO2018226707A1 (en) | 2017-06-07 | 2018-12-13 | Kci Licensing, Inc. | Composite dressings for improved granulation reduced maceration with negative-pressure treatment |
| US11207217B2 (en) | 2017-06-07 | 2021-12-28 | Kci Licensing, Inc. | Methods for manufacturing and assembling dual material tissue interface for negative-pressure therapy |
| JP2020523078A (ja) | 2017-06-07 | 2020-08-06 | ケーシーアイ ライセンシング インコーポレイテッド | 陰圧治療による肉芽形成の促進及び浸軟の低減のための複合ドレッシング |
| US11351063B2 (en) | 2017-06-07 | 2022-06-07 | Kci Licensing, Inc. | Composite dressings for improved granulation and reduced maceration with negative-pressure treatment |
| US10695227B2 (en) | 2017-06-07 | 2020-06-30 | Kci Licensing, Inc. | Methods for manufacturing and assembling dual material tissue interface for negative-pressure therapy |
| AU2018282148A1 (en) | 2017-06-07 | 2019-10-31 | 3M Innovative Properties Company | Composite dressings for improved granulation and reduced maceration with negative-pressure treatment |
| CN110799222B (zh) | 2017-06-07 | 2023-03-07 | 3M创新知识产权公司 | 用于减少组织向内生长的负压治疗的系统、设备以及方法 |
| SG11201909388RA (en) * | 2017-06-07 | 2019-11-28 | Kci Licensing Inc | Peel and place dressing for thick exudate and instillation |
| CA3065521A1 (en) | 2017-06-07 | 2018-12-13 | Kci Licensing, Inc. | Multi-layer wound filler for extended wear time |
| GB201713511D0 (en) | 2017-08-23 | 2017-10-04 | Scapa Uk Ltd | Wound dressing |
| KR102097594B1 (ko) * | 2017-11-28 | 2020-04-06 | 주식회사 영우 | 자외선 경화형 하이드로콜로이드 및 이의 제조방법 |
| GB201811449D0 (en) | 2018-07-12 | 2018-08-29 | Smith & Nephew | Apparatuses and methods for negative pressure wound therapy |
| US11998654B2 (en) | 2018-07-12 | 2024-06-04 | Bard Shannon Limited | Securing implants and medical devices |
| EP3846939B1 (en) | 2018-09-05 | 2023-05-03 | Hero Scientific Ltd | Testing for particulates |
| WO2020201878A1 (en) | 2019-04-01 | 2020-10-08 | 3M Innovative Properties Company | Process for making pressure sensitive adhesive hydrogels |
| WO2021048357A1 (en) * | 2019-09-11 | 2021-03-18 | Universiteit Gent | Anti-microbial hydrogel |
| CN115103866A (zh) * | 2019-11-29 | 2022-09-23 | 昭和电工材料株式会社 | 含有具有聚氧亚烷基链的化合物的组合物套组 |
| GB202000574D0 (en) | 2020-01-15 | 2020-02-26 | Smith & Nephew | Fluidic connectors for negative pressure wound therapy |
| EP4118412A1 (en) | 2020-03-11 | 2023-01-18 | Hero Scientific Ltd | Testing devices |
| CA3202405A1 (en) | 2021-01-06 | 2022-07-14 | Zvi Feldman | Filtration sampling devices |
| CN115260690B (zh) * | 2022-07-28 | 2023-05-30 | 复旦大学 | 一种可见光响应的超分子水凝胶及其制备方法和应用 |
Family Cites Families (67)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA677797A (en) | 1955-11-18 | 1964-01-14 | Minnesota Mining And Manufacturing Company | Sheet material having a pressure-sensitive adhesive coating of acrylate ester copolymer |
| US3121021A (en) | 1960-04-18 | 1964-02-11 | Minnesota Mining & Mfg | Breathable surgical adhesive tapes |
| US4112213A (en) | 1964-09-28 | 1978-09-05 | Johnson & Johnson | Pressure sensitive adhesive tapes and method of making same |
| US3389827A (en) | 1967-04-10 | 1968-06-25 | Minnesota Mining & Mfg | Easy-open container and sealing tape |
| JPS585320A (ja) | 1981-07-01 | 1983-01-12 | Toray Ind Inc | グラフト共重合体 |
| US4499896A (en) | 1982-03-30 | 1985-02-19 | Minnesota Mining And Manufacturing Co. | Reservoir wound dressing |
| US4538603A (en) | 1982-04-22 | 1985-09-03 | E. R. Squibb & Sons, Inc. | Dressings, granules, and their use in treating wounds |
| JPS59501210A (ja) * | 1982-07-03 | 1984-07-12 | スミス アンド ネフユ− アソシエイテツド コンパニ−ズ ピ−エルシ− | 重合性化合物 |
| JPS597687A (ja) | 1982-07-05 | 1984-01-14 | 株式会社北川機械製作所 | 建設資材搬入用クレ−ン装置 |
| EP0140941A1 (en) | 1983-04-07 | 1985-05-15 | Minnesota Mining And Manufacturing Company | Adhesive and adhesive-coated sheet material for moist skin |
| US4554297A (en) | 1983-04-18 | 1985-11-19 | Personal Products Company | Resilient cellular polymers from amine terminated poly(oxyalkylene) and polyfunctional epoxides |
| US4813875A (en) | 1984-07-31 | 1989-03-21 | Dentsply Research & Development Corp. | Chain extended urethane diacrylate and dental impression formation |
| SE444950B (sv) | 1984-09-28 | 1986-05-20 | Ytkemiska Inst | Ytbelagd artikel, forfarande och medel for framstellning derav samt anvendning derav |
| US4598004A (en) | 1985-01-24 | 1986-07-01 | Minnesota Mining And Manufacturing Company | Thin film surgical dressing with delivery system |
| GB8521254D0 (en) | 1985-08-24 | 1985-10-02 | Smith & Nephew Ass | Contoured film |
| US4738257A (en) | 1986-06-11 | 1988-04-19 | Hollister Incorporated | Occlusive wound care dressing |
| US4909244B1 (en) | 1986-11-26 | 1994-07-05 | Kendall & Co | Hydrogel wound dressing |
| GB8709498D0 (en) | 1987-04-22 | 1987-05-28 | Bay M | Wound dressing |
| US5018515A (en) | 1987-12-14 | 1991-05-28 | The Kendall Company | See through absorbent dressing |
| US4935087A (en) | 1987-12-14 | 1990-06-19 | The Kendall Company | Method of making an absorbent dressing |
| US4979946A (en) | 1987-12-14 | 1990-12-25 | The Kendall Company | Environmental absorbent dressing |
| JPH01174516A (ja) * | 1987-12-28 | 1989-07-11 | Mitsui Petrochem Ind Ltd | フッ素含有硬化性組成物 |
| US4849458A (en) | 1988-06-17 | 1989-07-18 | Matrix Medica, Inc. | Segmented polyether polyurethane |
| US4909243A (en) | 1988-07-20 | 1990-03-20 | E. R. Squibb & Sons, Inc. | Wound dressing system |
| US5088483A (en) | 1988-11-04 | 1992-02-18 | Minnesota Mining And Manufacturing Co. | Adhesive frame bandage |
| GB8906100D0 (en) | 1989-03-16 | 1989-04-26 | Smith & Nephew | Laminates |
| US5059424A (en) | 1989-11-01 | 1991-10-22 | Ndm Acquisition Corp. | Hydrogel wound dressing product |
| US5219564A (en) | 1990-07-06 | 1993-06-15 | Enzon, Inc. | Poly(alkylene oxide) amino acid copolymers and drug carriers and charged copolymers based thereon |
| US5254723A (en) | 1992-11-23 | 1993-10-19 | Arco Chemical Technology, L.P. | Preparation of glycol diesters from polyethers |
| US5429590A (en) | 1992-12-01 | 1995-07-04 | Nitto Denko Corporation | Medical water-absorptive polymer and dressing for wound and medical bandage using the same |
| AU682853B2 (en) | 1993-03-22 | 1997-10-23 | Minnesota Mining And Manufacturing Company | Windowless frame delivered dressing and method of manufacture |
| US5407717A (en) | 1993-04-14 | 1995-04-18 | Minnesota Mining And Manufacturing Company | Crosslinked absorbent pressure sensitive adhesive and wound dressing |
| US5603946A (en) | 1993-10-08 | 1997-02-18 | Bristol-Myers Squibb Company | Wound dressing |
| JP3717952B2 (ja) | 1994-04-01 | 2005-11-16 | ミネソタ マイニング アンド マニュファクチャリング カンパニー | 医療用粘着剤及びこれを有する医療用ドレッシング材 |
| KR0141431B1 (ko) * | 1994-05-17 | 1998-07-01 | 김상웅 | 생분해성 하이드로겔 고분자 |
| US5653699A (en) | 1994-09-13 | 1997-08-05 | Polymedica Industries, Inc. | Spyrosorbent wound dressings for exudate management |
| US5614310A (en) | 1994-11-04 | 1997-03-25 | Minnesota Mining And Manufacturing Company | Low trauma wound dressing with improved moisture vapor permeability |
| WO1997005185A2 (en) | 1995-07-28 | 1997-02-13 | Focal, Inc. | Multiblock biodegradable hydrogels for use as controlled release agents for drugs delivery and tissue treatment agents |
| GB9519574D0 (en) | 1995-09-26 | 1995-11-29 | Smith & Nephew | Conformable absorbent dressing |
| DE19543366C2 (de) * | 1995-11-21 | 1998-09-10 | Stockhausen Chem Fab Gmbh | Mit ungesättigten Aminoalkoholen vernetzte, wasserquellbare Polymerisate, deren Herstellung und Verwendung |
| US5968001A (en) | 1996-05-14 | 1999-10-19 | Bristol-Myers Squibb Company | Wound dressings with leak prevention seal |
| US5932200A (en) | 1996-08-14 | 1999-08-03 | Tyndale Plains-Hunter, Ltd. | Polyether polyurethane polymers, gels, solutions and uses thereof |
| US5733570A (en) | 1996-09-05 | 1998-03-31 | Minnesota Mining And Manufacturing Company | Absorbent dressing |
| WO1998012274A1 (en) * | 1996-09-23 | 1998-03-26 | Chandrashekar Pathak | Methods and devices for preparing protein concentrates |
| US5849325A (en) | 1996-10-07 | 1998-12-15 | Minnesota Mining And Manufacturing Company | Moisture-regulating adhesive dressing |
| GB9621956D0 (en) | 1996-10-22 | 1996-12-18 | Smith & Nephew | Absorbent dressing |
| JP3474381B2 (ja) | 1996-12-03 | 2003-12-08 | ニチバン株式会社 | 皮膚貼付用粘着剤組成物 |
| TW425403B (en) | 1997-02-04 | 2001-03-11 | Novartis Ag | Branched polyurethane (meth)acrylate prepolymers, opthal-mic mouldings derived therefrom and processes for their manufacture |
| NZ502417A (en) | 1997-07-31 | 2001-06-29 | Bristol Myers Squibb Co | Non-adherent wound dressing |
| US6420622B1 (en) | 1997-08-01 | 2002-07-16 | 3M Innovative Properties Company | Medical article having fluid control film |
| GB9717357D0 (en) | 1997-08-16 | 1997-10-22 | Bristol Myers Squibb Co | Multi layered wound dressing |
| CA2304096C (en) | 1997-09-18 | 2003-09-09 | Pacira Pharmaceuticals, Inc. | Sustained-release liposomal anesthetic compositions |
| FR2768341B1 (fr) | 1997-09-18 | 2000-04-14 | Lab Francais Du Fractionnement | Composition pharmaceutique placebo lyophilisable destinee a imiter un medicament, notamment a base de proteines ou de polypeptides |
| US6171985B1 (en) | 1997-12-01 | 2001-01-09 | 3M Innovative Properties Company | Low trauma adhesive article |
| US6353069B1 (en) * | 1998-04-15 | 2002-03-05 | Alcon Manufacturing, Ltd. | High refractive index ophthalmic device materials |
| GB2341185A (en) | 1998-09-07 | 2000-03-08 | Polybiomed Ltd | Polymerizable material and adhesive sheet material therefrom; dressings, electrodes and transdermal patches |
| US6198016B1 (en) | 1998-12-01 | 2001-03-06 | 3M Innovative Properties Company | Wet skin adhesive article |
| WO2000056830A1 (en) * | 1999-03-19 | 2000-09-28 | Minnesota Mining And Manufacturing Company | Plasticized pressure sensitive adhesive |
| WO2001041687A1 (en) | 1999-12-09 | 2001-06-14 | The Procter & Gamble Company | Disposable absorbent article employing odor reduction layer containing metalphthalocyanine material |
| US6566575B1 (en) | 2000-02-15 | 2003-05-20 | 3M Innovative Properties Company | Patterned absorbent article for wound dressing |
| CA2400228C (en) * | 2000-03-10 | 2008-11-18 | 3M Innovative Properties Company | Medical dressings with multiple adhesives and methods of manufacturing |
| US7067228B2 (en) * | 2000-06-22 | 2006-06-27 | Hitachi Chemical Co., Ltd. | Photosensitive resin composition, photosensitive element employing it, resist pattern forming method, and printed wiring board fabrication method |
| US6903243B1 (en) | 2000-09-08 | 2005-06-07 | 3M Innovative Properties Company | Multi-layer absorbent wound dressing |
| US20030044468A1 (en) * | 2001-03-20 | 2003-03-06 | Francesco Cellesi | Two-phase processing of thermosensitive polymers for use as biomaterials |
| US7651695B2 (en) * | 2001-05-18 | 2010-01-26 | Advanced Cardiovascular Systems, Inc. | Medicated stents for the treatment of vascular disease |
| US7204997B2 (en) * | 2002-01-29 | 2007-04-17 | Supratek Pharma Inc. | Responsive microgel and methods related thereto |
| US6960275B2 (en) * | 2002-04-12 | 2005-11-01 | 3M Innovative Properties Company | Method of making a viscoelastic article by coating and curing on a reusable surface |
-
2002
- 2002-04-12 US US10/121,518 patent/US7005143B2/en not_active Expired - Lifetime
-
2003
- 2003-03-27 DE DE60318189T patent/DE60318189T2/de not_active Expired - Lifetime
- 2003-03-27 JP JP2003583503A patent/JP4550428B2/ja not_active Expired - Lifetime
- 2003-03-27 EP EP03726141A patent/EP1494727B1/en not_active Expired - Lifetime
- 2003-03-27 CA CA2481765A patent/CA2481765C/en not_active Expired - Fee Related
- 2003-03-27 MX MXPA04009963A patent/MXPA04009963A/es active IP Right Grant
- 2003-03-27 EP EP07123358.9A patent/EP1897566B1/en not_active Expired - Lifetime
- 2003-03-27 CN CNB038137631A patent/CN1327908C/zh not_active Expired - Lifetime
- 2003-03-27 AT AT03726141T patent/ATE381355T1/de not_active IP Right Cessation
- 2003-03-27 KR KR1020047016253A patent/KR100982415B1/ko not_active Expired - Fee Related
- 2003-03-27 AU AU2003228392A patent/AU2003228392A1/en not_active Abandoned
- 2003-03-27 BR BRPI0309109A patent/BRPI0309109B8/pt not_active IP Right Cessation
- 2003-03-27 ES ES03726141T patent/ES2297161T3/es not_active Expired - Lifetime
- 2003-03-27 WO PCT/US2003/009556 patent/WO2003086493A1/en not_active Ceased
-
2005
- 2005-10-21 US US11/255,396 patent/US20060039982A1/en not_active Abandoned
Also Published As
| Publication number | Publication date |
|---|---|
| CN1327908C (zh) | 2007-07-25 |
| DE60318189T2 (de) | 2008-12-18 |
| BRPI0309109B1 (pt) | 2016-12-13 |
| DE60318189D1 (de) | 2008-01-31 |
| KR100982415B1 (ko) | 2010-09-16 |
| US7005143B2 (en) | 2006-02-28 |
| JP2005533531A (ja) | 2005-11-10 |
| CA2481765A1 (en) | 2003-10-23 |
| US20060039982A1 (en) | 2006-02-23 |
| JP4550428B2 (ja) | 2010-09-22 |
| ATE381355T1 (de) | 2008-01-15 |
| EP1494727B1 (en) | 2007-12-19 |
| US20030203011A1 (en) | 2003-10-30 |
| BR0309109A (pt) | 2005-02-01 |
| ES2297161T3 (es) | 2008-05-01 |
| EP1897566A1 (en) | 2008-03-12 |
| CA2481765C (en) | 2011-09-13 |
| EP1494727A1 (en) | 2005-01-12 |
| CN1658912A (zh) | 2005-08-24 |
| WO2003086493A1 (en) | 2003-10-23 |
| AU2003228392A1 (en) | 2003-10-27 |
| KR20040101445A (ko) | 2004-12-02 |
| EP1897566B1 (en) | 2017-02-22 |
| BRPI0309109B8 (pt) | 2021-06-22 |
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