USRE33839E - Absorbents for blood and serous body fluids - Google Patents
Absorbents for blood and serous body fluids Download PDFInfo
- Publication number
- USRE33839E USRE33839E US07/629,095 US62909590A USRE33839E US RE33839 E USRE33839 E US RE33839E US 62909590 A US62909590 A US 62909590A US RE33839 E USRE33839 E US RE33839E
- Authority
- US
- United States
- Prior art keywords
- component
- acid
- acids
- absorbent according
- absorbent
- 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 - Lifetime
Links
- 239000002250 absorbent Substances 0.000 title claims abstract description 51
- 230000002745 absorbent Effects 0.000 title claims abstract description 51
- 239000008280 blood Substances 0.000 title claims abstract description 30
- 210000004369 blood Anatomy 0.000 title claims abstract description 30
- 210000001124 body fluid Anatomy 0.000 title claims abstract description 10
- 239000010839 body fluid Substances 0.000 title claims abstract description 10
- 229920001577 copolymer Polymers 0.000 claims abstract description 15
- 229920005615 natural polymer Polymers 0.000 claims abstract description 3
- 229920001059 synthetic polymer Polymers 0.000 claims abstract description 3
- 239000002253 acid Substances 0.000 claims description 30
- 229920000642 polymer Polymers 0.000 claims description 18
- 150000003839 salts Chemical class 0.000 claims description 18
- 150000007513 acids Chemical class 0.000 claims description 17
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 15
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims description 12
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 12
- -1 hydrosulphates Chemical class 0.000 claims description 9
- 150000007522 mineralic acids Chemical class 0.000 claims description 9
- 229920002472 Starch Polymers 0.000 claims description 8
- 229920002678 cellulose Polymers 0.000 claims description 8
- 239000001913 cellulose Substances 0.000 claims description 8
- 150000001875 compounds Chemical class 0.000 claims description 8
- 239000008107 starch Substances 0.000 claims description 8
- 235000019698 starch Nutrition 0.000 claims description 8
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 claims description 7
- 150000001408 amides Chemical class 0.000 claims description 7
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims description 6
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical class OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 claims description 6
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Natural products NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims description 6
- 239000000843 powder Substances 0.000 claims description 6
- 239000011734 sodium Substances 0.000 claims description 6
- 150000001299 aldehydes Chemical class 0.000 claims description 5
- 230000000266 injurious effect Effects 0.000 claims description 5
- FQPSGWSUVKBHSU-UHFFFAOYSA-N methacrylamide Chemical compound CC(=C)C(N)=O FQPSGWSUVKBHSU-UHFFFAOYSA-N 0.000 claims description 5
- 150000007524 organic acids Chemical class 0.000 claims description 5
- RYECOJGRJDOGPP-UHFFFAOYSA-N Ethylurea Chemical compound CCNC(N)=O RYECOJGRJDOGPP-UHFFFAOYSA-N 0.000 claims description 4
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 claims description 4
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric Acid Chemical class [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 claims description 4
- 235000011037 adipic acid Nutrition 0.000 claims description 4
- 150000001298 alcohols Chemical class 0.000 claims description 4
- 239000011575 calcium Substances 0.000 claims description 4
- 150000001732 carboxylic acid derivatives Chemical class 0.000 claims description 4
- 150000001735 carboxylic acids Chemical class 0.000 claims description 4
- 235000015165 citric acid Nutrition 0.000 claims description 4
- 150000002763 monocarboxylic acids Chemical class 0.000 claims description 4
- BDHFUVZGWQCTTF-UHFFFAOYSA-N sulfonic acid Chemical compound OS(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-N 0.000 claims description 4
- 235000002906 tartaric acid Nutrition 0.000 claims description 4
- UMGDCJDMYOKAJW-UHFFFAOYSA-N thiourea Chemical compound NC(N)=S UMGDCJDMYOKAJW-UHFFFAOYSA-N 0.000 claims description 4
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 claims description 3
- 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 claims description 3
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims description 3
- 229930006000 Sucrose Natural products 0.000 claims description 3
- CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 claims description 3
- WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 claims description 3
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 claims description 3
- 239000004327 boric acid Substances 0.000 claims description 3
- 150000001991 dicarboxylic acids Chemical class 0.000 claims description 3
- 235000013681 dietary sucrose Nutrition 0.000 claims description 3
- 239000008103 glucose Substances 0.000 claims description 3
- 239000011777 magnesium Substances 0.000 claims description 3
- 238000000034 method Methods 0.000 claims description 3
- 150000002772 monosaccharides Chemical class 0.000 claims description 3
- 229920001542 oligosaccharide Polymers 0.000 claims description 3
- 150000002482 oligosaccharides Chemical class 0.000 claims description 3
- 229920001282 polysaccharide Polymers 0.000 claims description 3
- 239000005017 polysaccharide Substances 0.000 claims description 3
- 239000011591 potassium Substances 0.000 claims description 3
- 229910052700 potassium Inorganic materials 0.000 claims description 3
- 229910052708 sodium Inorganic materials 0.000 claims description 3
- 229960004793 sucrose Drugs 0.000 claims description 3
- QNIRRHUUOQAEPB-UHFFFAOYSA-N 2-(prop-2-enoylamino)butane-2-sulfonic acid Chemical compound CCC(C)(S(O)(=O)=O)NC(=O)C=C QNIRRHUUOQAEPB-UHFFFAOYSA-N 0.000 claims description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims description 2
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 claims description 2
- WQZGKKKJIJFFOK-QTVWNMPRSA-N D-mannopyranose Chemical compound OC[C@H]1OC(O)[C@@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-QTVWNMPRSA-N 0.000 claims description 2
- 229930091371 Fructose Natural products 0.000 claims description 2
- RFSUNEUAIZKAJO-ARQDHWQXSA-N Fructose Chemical compound OC[C@H]1O[C@](O)(CO)[C@@H](O)[C@@H]1O RFSUNEUAIZKAJO-ARQDHWQXSA-N 0.000 claims description 2
- 239000005715 Fructose Substances 0.000 claims description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 2
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 claims description 2
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 claims description 2
- 229910019142 PO4 Inorganic materials 0.000 claims description 2
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims description 2
- 235000011054 acetic acid Nutrition 0.000 claims description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 2
- 229910052782 aluminium Inorganic materials 0.000 claims description 2
- 229910000147 aluminium phosphate Inorganic materials 0.000 claims description 2
- 229910052791 calcium Inorganic materials 0.000 claims description 2
- BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical class OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 claims description 2
- 150000004649 carbonic acid derivatives Chemical class 0.000 claims description 2
- 235000019253 formic acid Nutrition 0.000 claims description 2
- 239000001257 hydrogen Substances 0.000 claims description 2
- 229910052739 hydrogen Inorganic materials 0.000 claims description 2
- 150000004694 iodide salts Chemical class 0.000 claims description 2
- 159000000014 iron salts Chemical class 0.000 claims description 2
- 229910052744 lithium Inorganic materials 0.000 claims description 2
- 229910052749 magnesium Inorganic materials 0.000 claims description 2
- 150000002823 nitrates Chemical class 0.000 claims description 2
- 235000021317 phosphate Nutrition 0.000 claims description 2
- 150000003013 phosphoric acid derivatives Chemical class 0.000 claims description 2
- 150000003467 sulfuric acid derivatives Chemical class 0.000 claims description 2
- 239000004753 textile Substances 0.000 claims description 2
- 239000011701 zinc Substances 0.000 claims description 2
- 229910052725 zinc Inorganic materials 0.000 claims description 2
- PNJWIWWMYCMZRO-UHFFFAOYSA-N 4-penten-2-one Chemical compound CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 claims 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims 1
- XGEGHDBEHXKFPX-UHFFFAOYSA-N N-methylthiourea Natural products CNC(N)=O XGEGHDBEHXKFPX-UHFFFAOYSA-N 0.000 claims 1
- 150000001279 adipic acids Chemical class 0.000 claims 1
- 239000004411 aluminium Substances 0.000 claims 1
- 150000003842 bromide salts Chemical class 0.000 claims 1
- 150000003841 chloride salts Chemical class 0.000 claims 1
- 150000004676 glycans Chemical class 0.000 claims 1
- XGEGHDBEHXKFPX-NJFSPNSNSA-N methylurea Chemical compound [14CH3]NC(N)=O XGEGHDBEHXKFPX-NJFSPNSNSA-N 0.000 claims 1
- 239000006069 physical mixture Substances 0.000 claims 1
- 210000004911 serous fluid Anatomy 0.000 claims 1
- 150000003460 sulfonic acids Chemical class 0.000 claims 1
- 239000007787 solid Substances 0.000 abstract description 7
- 238000010521 absorption reaction Methods 0.000 abstract description 4
- 150000002484 inorganic compounds Chemical group 0.000 abstract description 3
- 150000002894 organic compounds Chemical group 0.000 abstract description 3
- 229910010272 inorganic material Chemical group 0.000 abstract 1
- 230000014759 maintenance of location Effects 0.000 abstract 1
- 239000000306 component Substances 0.000 description 24
- 238000006116 polymerization reaction Methods 0.000 description 15
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 14
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 12
- 235000010980 cellulose Nutrition 0.000 description 7
- 239000011780 sodium chloride Substances 0.000 description 7
- 235000017557 sodium bicarbonate Nutrition 0.000 description 6
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 6
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Natural products OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 5
- 239000003054 catalyst Substances 0.000 description 4
- KGMXPXPXPAAUMD-UHFFFAOYSA-N propane;dihydrochloride Chemical compound Cl.Cl.CCC KGMXPXPXPAAUMD-UHFFFAOYSA-N 0.000 description 4
- 239000012503 blood component Substances 0.000 description 3
- USHAGKDGDHPEEY-UHFFFAOYSA-L potassium persulfate Chemical compound [K+].[K+].[O-]S(=O)(=O)OOS([O-])(=O)=O USHAGKDGDHPEEY-UHFFFAOYSA-L 0.000 description 3
- DLFVBJFMPXGRIB-UHFFFAOYSA-N Acetamide Chemical compound CC(N)=O DLFVBJFMPXGRIB-UHFFFAOYSA-N 0.000 description 2
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- 229920000881 Modified starch Polymers 0.000 description 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 239000004202 carbamide Substances 0.000 description 2
- 239000001768 carboxy methyl cellulose Substances 0.000 description 2
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 2
- 239000008112 carboxymethyl-cellulose Substances 0.000 description 2
- 239000004222 ferrous gluconate Substances 0.000 description 2
- 235000013924 ferrous gluconate Nutrition 0.000 description 2
- 229920013821 hydroxy alkyl cellulose Polymers 0.000 description 2
- VRIVJOXICYMTAG-IYEMJOQQSA-L iron(ii) gluconate Chemical compound [Fe+2].OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C([O-])=O.OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C([O-])=O VRIVJOXICYMTAG-IYEMJOQQSA-L 0.000 description 2
- 229920000609 methyl cellulose Polymers 0.000 description 2
- 239000001923 methylcellulose Substances 0.000 description 2
- 235000019426 modified starch Nutrition 0.000 description 2
- 235000005985 organic acids Nutrition 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 150000004804 polysaccharides Chemical class 0.000 description 2
- HRZFUMHJMZEROT-UHFFFAOYSA-L sodium disulfite Chemical compound [Na+].[Na+].[O-]S(=O)S([O-])(=O)=O HRZFUMHJMZEROT-UHFFFAOYSA-L 0.000 description 2
- 235000010262 sodium metabisulphite Nutrition 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- UDJZTGMLYITLIQ-UHFFFAOYSA-N 1-ethenylpyrrolidine Chemical compound C=CN1CCCC1 UDJZTGMLYITLIQ-UHFFFAOYSA-N 0.000 description 1
- BXAAQNFGSQKPDZ-UHFFFAOYSA-N 3-[1,2,2-tris(prop-2-enoxy)ethoxy]prop-1-ene Chemical compound C=CCOC(OCC=C)C(OCC=C)OCC=C BXAAQNFGSQKPDZ-UHFFFAOYSA-N 0.000 description 1
- PXRKCOCTEMYUEG-UHFFFAOYSA-N 5-aminoisoindole-1,3-dione Chemical compound NC1=CC=C2C(=O)NC(=O)C2=C1 PXRKCOCTEMYUEG-UHFFFAOYSA-N 0.000 description 1
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonium chloride Substances [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 1
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
- KRKNYBCHXYNGOX-UHFFFAOYSA-K Citrate Chemical compound [O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O KRKNYBCHXYNGOX-UHFFFAOYSA-K 0.000 description 1
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 1
- 241001460678 Napo <wasp> Species 0.000 description 1
- 229920005372 Plexiglas® Polymers 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 239000002671 adjuvant Substances 0.000 description 1
- 239000000783 alginic acid Substances 0.000 description 1
- 235000010443 alginic acid Nutrition 0.000 description 1
- 229920000615 alginic acid Polymers 0.000 description 1
- 229960001126 alginic acid Drugs 0.000 description 1
- 150000004781 alginic acids Chemical class 0.000 description 1
- 229920013820 alkyl cellulose Polymers 0.000 description 1
- 235000011114 ammonium hydroxide Nutrition 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 230000004888 barrier function Effects 0.000 description 1
- 230000001588 bifunctional effect Effects 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 150000001649 bromium compounds Chemical class 0.000 description 1
- 125000006297 carbonyl amino group Chemical group [H]N([*:2])C([*:1])=O 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 150000001805 chlorine compounds Chemical class 0.000 description 1
- 239000000645 desinfectant Substances 0.000 description 1
- 150000001470 diamides Chemical class 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 239000000194 fatty acid Chemical class 0.000 description 1
- 229930195729 fatty acid Chemical class 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Substances [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 150000002688 maleic acid derivatives Chemical class 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 125000005395 methacrylic acid group Chemical group 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 229920001206 natural gum Polymers 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 239000002304 perfume Substances 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 239000004926 polymethyl methacrylate Substances 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- AAYRWMCIKCRHIN-UHFFFAOYSA-N propane-1-sulfonic acid;prop-2-enamide Chemical compound NC(=O)C=C.CCCS(O)(=O)=O AAYRWMCIKCRHIN-UHFFFAOYSA-N 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- JXAZAUKOWVKTLO-UHFFFAOYSA-L sodium pyrosulfate Chemical compound [Na+].[Na+].[O-]S(=O)(=O)OS([O-])(=O)=O JXAZAUKOWVKTLO-UHFFFAOYSA-L 0.000 description 1
- RPACBEVZENYWOL-XFULWGLBSA-M sodium;(2r)-2-[6-(4-chlorophenoxy)hexyl]oxirane-2-carboxylate Chemical compound [Na+].C=1C=C(Cl)C=CC=1OCCCCCC[C@]1(C(=O)[O-])CO1 RPACBEVZENYWOL-XFULWGLBSA-M 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- 229940095064 tartrate Drugs 0.000 description 1
- 150000003672 ureas Chemical class 0.000 description 1
- 210000002700 urine Anatomy 0.000 description 1
- 239000000230 xanthan gum Substances 0.000 description 1
- 229920001285 xanthan gum Polymers 0.000 description 1
- 235000010493 xanthan gum Nutrition 0.000 description 1
- 229940082509 xanthan gum Drugs 0.000 description 1
Classifications
-
- 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
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S977/00—Nanotechnology
- Y10S977/902—Specified use of nanostructure
- Y10S977/904—Specified use of nanostructure for medical, immunological, body treatment, or diagnosis
- Y10S977/905—Specially adapted for travel through blood circulatory system
Definitions
- the invention concerns absorbents for blood and other serous body fluids which are suitable for use in absorbent throw-away products for surgical and other medical purposes as well as for sanitary napkins.
- starch such as, e.g., starch-acrylonitrile graft polymerizates (U.S. Pat. No. 3,997,484; 3,661,815; 4,155,888; 3,935,099), gelatinized starch derivatives (DE-OS No. 2,702,781), starch-acryloamideacryloamidopropane sulphonic acid graft polymerizate (U.S. patent application Ser. No. 955,827), or on cellulose, such as derivatives of alkyl or hydroxyalkyl cellulose (Jap. Pat. No.
- a partial improvement of blood dispersibility of the absorbent was obtained in accordance with DE-OS No. 2,844,956 and EUP No. 0,009,977 in that a partly synthetic or fully synthetic absorbent in powder form is subsequently treated with polyethers (DE-OS No. 2,844,956) or with fat alcohols, fatty acids or fat esters (EUP No. 0,009,977), mostly dissolved in organic solvents.
- the subject of the invention is an absorbent for blood and serous body fluids which is characterized in that it comprises at least two components, A and B, whereby component A is at least one water-swellable synthetic or natural polymer or copolymer and component B is at least one inorganic and/or organic compound which at normal temperature is present in form of a pourable powder and is water-soluble.
- Suitable as Component A are the water-swellable polysaccharide polymers, such as cellulose, cellulose derivatives, such as carboxymethyl cellulose, alkyl or hydroxyalkyl cellulose, starch and starch derivatives and natural gums (xanthan gum, alginic acid) and their salts as well as the polymers and copolymers of (meth)acrylic acid or (meth)acrylic acid derivatives, mainly homo- or copolymers of acrylic, methacrylic, acrylamidomethylpropane sulphonic acid, the salts of the aforegoing acids; of acrylic or methacrylic amide with each other or with vinyl pyrrolidone and/or vinyl acetate.
- the aforementioned polymers may be cross-linked by at least one bifunctional netting agent so that they are only swellable but not soluble in water. All of the polymers are produced in accordance with known methods.
- Suitable as component B are inorganic or organic compounds which are solid at ambient temperature, preferably in form of a pourable powder.
- Component B Especially suitable as Component B are water-soluble salts of organic or inorganic acids not injurious to health, inorganic acids or organic mono- or polycarboxylic acids or low-molecular polymer carboxylic or sulphonic acids, solid at normal temperature, powdered and not injurious to health or also derivatives of carboxylic acids or mono- and oligosaccharides solid at normal temperature and not injurious to health.
- salts of inorganic acids which are not injurious to health are preferred the chlorides, bromides, iodides, sulphates, hydrosulphates, phosphates, hydrogen or dihydrogen phosphates, tetraborates, nitrates, carbonates or hydrogen carbonates, as salts of organic carboxylic acids the salts of acetic, formic, adipic, citric or tartaric acids or also the salts of low-molecular polymeric carboxylic and/or sulphonic acids having molecular masses ranging from 300 to 100,000, preferably 2,000 to 20,000, or homo- or copolymerizates of unsaturated mono- or dicarboxylic acids, sulphonic acids, aldehydes, alcohols as well as (meth)acryloamide.
- Suitable salts are the ammonium, sodium, potassium, lithium, calcium, magnesium, zinc, aluminum or iron salts of the inorganic or organic acid.
- inorganic or organic acids proper as component B there may also be used inorganic or organic acids proper as component B, provided they are solid at normal temperature, are powdered and water-soluble.
- Suitable inorganic acids are boric acid or phosphoric acid.
- Suitable organic acids are mono- or polycarboxylic acids, such as citric, tartaric or adipic acid or low-molecular polymeric carboxylic or sulphonic acids with molecular masses ranging from 300 to 100,000 g/mole, preferably 2,000 to 20,000 g/mole based on homo- or copolymerizates of unsaturated mono- or dicarboxylic acids, sulphonic acids, aldehydes, alcohols as well as (meth)acrylamide.
- Suitable are, furthermore, the water-soluble derivatives of carboxylic acid, solid at normal temperature, such as amides or diamides, preferably acetamide, urea and urea derivatives, such as thiourea, methyl or ethyl urea.
- component B mono- or oligosaccharides, such as glucose, fructose, mannose or saccharose.
- the absorbent is composed of components A and B at a weight ratio of 25 to 98 weight %, preferably 50 to 90 weight %, of component A to 2 to 75 weight %, preferably 10 to 50 weight %, of component B.
- Mixing of the two components, A and B may be obtained in that component B is already dissolved in the monomer solution prior to polymerization, or in that component B is added to the process at any time in dry or dissolved form.
- the absorbent in accordance with the invention due to its composition, is suitable to absorb and/or retain blood and other serous body fluids, in particular for use in absorbent throw-away products, such as sanitary napkins, tampons or absorbent products for surgical and medical purposes.
- the absorbent in accordance with the invention is sprinkled onto or over a textile or paper support in some suitable dosage and is fixed in or on the material by some suitable measures.
- the absorbents in accordance with the invention may be mixed with perfumes, binders or other adjuvants, too, such as, e.g., disinfectants, which do not influence the absorption properties of the absorbent.
- the individual components of the catalyst system (0.64 g sodium pyrosulfate, 0.36 g potassium persulfate and 0.03 g iron(II) gluconate dissolved in 60 g water were added at normal temperature whereby polymerization was started. Processing occurred as in Example 1.
- component A To the products obtained as per Examples 1 to 6 (component A) were mixed in powder form homogeneous the salts indicated in Table 1 (component B). The following testing method was employed in order to determine the speed of distribution of the blood in the absorbent and the quantity of blood retained by the absorbent:
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- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Epidemiology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Dispersion Chemistry (AREA)
- Hematology (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Materials For Medical Uses (AREA)
- Absorbent Articles And Supports Therefor (AREA)
- Solid-Sorbent Or Filter-Aiding Compositions (AREA)
- Medicines Containing Material From Animals Or Micro-Organisms (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE3128100 | 1981-07-16 | ||
| DE3128100A DE3128100C2 (de) | 1981-07-16 | 1981-07-16 | Absorptionsmittel für Blut und seröse Körperflüssigkeiten |
Related Parent Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US06928573 Reissue | 1982-07-10 | ||
| US07405616 Continuation | 1989-09-11 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| USRE33839E true USRE33839E (en) | 1992-03-03 |
Family
ID=6137040
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US07/629,095 Expired - Lifetime USRE33839E (en) | 1981-07-16 | 1982-07-10 | Absorbents for blood and serous body fluids |
| US06/928,573 Ceased US4693713A (en) | 1981-07-16 | 1982-07-10 | Absorbents for blood and serous body fluids |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US06/928,573 Ceased US4693713A (en) | 1981-07-16 | 1982-07-10 | Absorbents for blood and serous body fluids |
Country Status (6)
| Country | Link |
|---|---|
| US (2) | USRE33839E (cg-RX-API-DMAC7.html) |
| EP (1) | EP0071063B1 (cg-RX-API-DMAC7.html) |
| JP (1) | JPS58501107A (cg-RX-API-DMAC7.html) |
| AT (1) | ATE16891T1 (cg-RX-API-DMAC7.html) |
| DE (2) | DE3128100C2 (cg-RX-API-DMAC7.html) |
| WO (1) | WO1983000289A1 (cg-RX-API-DMAC7.html) |
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| BE793650A (fr) * | 1972-11-06 | 1973-07-03 | Union Carbide Corp | Polymeres particulaires meubles, insolubles et gonflables et procede pour les preparer |
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| FR2260961B1 (cg-RX-API-DMAC7.html) * | 1974-02-20 | 1977-06-10 | Roussel Uclaf | |
| NO136583C (no) * | 1974-09-12 | 1984-06-07 | Papirind Forskningsinst | Mekanisk tremasse med hoey absorpsjonshastighet, samt fremgangsmaate for fremstilling derav |
| US4090013A (en) * | 1975-03-07 | 1978-05-16 | National Starch And Chemical Corp. | Absorbent composition of matter |
| JPS5259651A (en) * | 1975-11-11 | 1977-05-17 | Kao Corp | Absorbent material |
| JPS5259086A (en) * | 1975-11-11 | 1977-05-16 | Kao Corp | Absorbing material |
| PH13425A (en) * | 1976-05-10 | 1980-04-23 | Du Pont | 2,3,8,12b-tetrahydro 1 h-3a,8-methano-dibenzo(3,4,6,7)cyclohepta(1,2-c)pyrrole derivatives pharmaceutical compositions containing same and method |
-
1981
- 1981-07-16 DE DE3128100A patent/DE3128100C2/de not_active Expired
-
1982
- 1982-07-10 JP JP57502173A patent/JPS58501107A/ja active Granted
- 1982-07-10 EP EP82106196A patent/EP0071063B1/de not_active Expired
- 1982-07-10 DE DE8282106196T patent/DE3267907D1/de not_active Expired
- 1982-07-10 US US07/629,095 patent/USRE33839E/en not_active Expired - Lifetime
- 1982-07-10 WO PCT/DE1982/000146 patent/WO1983000289A1/de not_active Ceased
- 1982-07-10 AT AT82106196T patent/ATE16891T1/de not_active IP Right Cessation
- 1982-07-10 US US06/928,573 patent/US4693713A/en not_active Ceased
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| US3121427A (en) * | 1960-06-13 | 1964-02-18 | Jack M Mosier | Catamenial appliance and composition |
| US3810468A (en) * | 1966-05-31 | 1974-05-14 | Dow Chemical Co | Sorbent |
| US4058124A (en) * | 1971-11-01 | 1977-11-15 | Union Carbide Corporation | Disposable absorbent articles containing particulate, free-flowing, insoluble swellable polymers |
| US4076663A (en) * | 1975-03-27 | 1978-02-28 | Sanyo Chemical Industries, Ltd. | Water absorbing starch resins |
| US4190563A (en) * | 1977-10-18 | 1980-02-26 | Lever Brothers Company, Inc. | Particulate absorbant material surface treated with polyether to improve dispersibility in blood |
| US4259383A (en) * | 1978-06-30 | 1981-03-31 | Sterling Drug Inc. | Disinfecting tissue |
| US4333461A (en) * | 1979-12-17 | 1982-06-08 | Colgate-Palmolive Company | Borated polysaccharide absorbents and absorbent products |
Cited By (38)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5712316A (en) * | 1993-07-09 | 1998-01-27 | Chemische Fabrik Stockhausen Gmbh | Powder-form cross-linked polymers capable of absorbing aqueous liquids and body fluids, method of preparing them and their use |
| EP1570869A1 (en) | 1994-02-17 | 2005-09-07 | Nippon Shokubai Co., Ltd. | Water absorbent agent, method for production thereof, and water absorbent composition |
| EP0668080A2 (en) | 1994-02-17 | 1995-08-23 | Nippon Shokubai Co., Ltd. | Water-absorbent agent, method for production thereof, and water-absorbent composition |
| US7250459B2 (en) | 1994-02-17 | 2007-07-31 | Nippon Shokubai Co., Ltd. | Absorbent resin composition |
| US5610208A (en) * | 1994-02-17 | 1997-03-11 | Nippon Shokubai Co., Ltd. | Water-absorbent agent, method for production thereof, and water-absorbent composition |
| US20060025536A1 (en) * | 1994-02-17 | 2006-02-02 | Nippon Shokubai Co., Ltd. | Absorbent resin composition |
| EP0668080A3 (en) * | 1994-02-17 | 1999-09-15 | Nippon Shokubai Co., Ltd. | Water-absorbent agent, method for production thereof, and water-absorbent composition |
| US6992144B2 (en) | 1994-02-17 | 2006-01-31 | Nippon Shokubai Co., Ltd. | Water-absorbent agent, method for production thereof, and water-absorbent composition |
| US5849816A (en) * | 1994-08-01 | 1998-12-15 | Leonard Pearlstein | Method of making high performance superabsorbent material |
| US5549590A (en) * | 1994-08-01 | 1996-08-27 | Leonard Pearlstein | High performance absorbent particles and methods of preparation |
| US5539019A (en) * | 1994-08-01 | 1996-07-23 | Leonard Pearlstein | High performance absorbent particles and methods of preparation |
| US6300275B1 (en) | 1997-04-29 | 2001-10-09 | The Dow Chemical Company | Resilient superabsorbent compositions |
| US6639119B2 (en) | 1998-06-29 | 2003-10-28 | The Procter & Gamble Company | Absorbent article including a reducing agent for feces |
| US6018093A (en) | 1998-06-29 | 2000-01-25 | The Procter & Gamble Company | Absorbent article including a calcium-based feces modification agent |
| US5998695A (en) | 1998-06-29 | 1999-12-07 | The Procter & Gamble Company | Absorbent article including ionic complexing agent for feces |
| US6169223B1 (en) | 1999-02-08 | 2001-01-02 | Internationale Verbandstoff Fabrik Schaffhausen | Compress for medical treatment |
| WO2000071176A1 (en) * | 1999-05-24 | 2000-11-30 | Kolon Chemical Co., Ltd. | Water-absorbent resin compound and processing |
| US20050181200A1 (en) * | 2001-12-14 | 2005-08-18 | Richard Mertens | Compacted absorbent polymers the production thereof and the use of the same |
| US8288002B2 (en) | 2003-07-25 | 2012-10-16 | Evonik Stockhausen Gmbh | Water-absorbing polymer particles with thermoplastic coating |
| US7842386B2 (en) | 2003-07-25 | 2010-11-30 | Evonik Stockhausen Gmbh | Powdery water-absorbing polymers with fine particles bound by thermoplastic adhesives |
| US20110015601A1 (en) * | 2003-07-25 | 2011-01-20 | Evonik Stockhausen Gmbh | Water-absorbing polymer particles with thermoplastic coating |
| US8518541B2 (en) | 2003-07-25 | 2013-08-27 | Evonik Stockhausen Gmbh | Powdery water-absorbing polymers with fine particles bound by thermoplastic adhesives |
| US20080032888A1 (en) * | 2004-05-07 | 2008-02-07 | Masatoshi Nakamura | Water Absorbing Agent and Production Method Thereof |
| US8846823B2 (en) | 2004-05-07 | 2014-09-30 | Nippon Shokubai Co., Ltd. | Water absorbing agent and production method thereof |
| US9062140B2 (en) | 2005-04-07 | 2015-06-23 | Nippon Shokubai Co., Ltd. | Polyacrylic acid (salt) water-absorbent resin, production process thereof, and acrylic acid used in polymerization for production of water-absorbent resin |
| US9926449B2 (en) | 2005-12-22 | 2018-03-27 | Nippon Shokubai Co., Ltd. | Water-absorbent resin composition, method of manufacturing the same, and absorbent article |
| US10358558B2 (en) | 2005-12-22 | 2019-07-23 | Nippon Shokubai Co., Ltd. | Water-absorbent resin composition, method of manufacturing the same, and absorbent article |
| US9090718B2 (en) | 2006-03-24 | 2015-07-28 | Nippon Shokubai Co., Ltd. | Water-absorbing resin and method for manufacturing the same |
| US20110136986A1 (en) * | 2008-08-12 | 2011-06-09 | Basf Se | Method for Producing Superabsorbers with a Low Residual Monomer Content |
| US8410233B2 (en) | 2008-08-12 | 2013-04-02 | Basf Se | Method for producing superabsorbers with a low residual monomer content |
| US9775927B2 (en) | 2009-09-29 | 2017-10-03 | Nippon Shokubai Co., Ltd. | Particulate water absorbent and process for production thereof |
| US8952116B2 (en) | 2009-09-29 | 2015-02-10 | Nippon Shokubai Co., Ltd. | Particulate water absorbent and process for production thereof |
| AU2016245416B2 (en) * | 2015-04-06 | 2020-08-13 | Upl Limited | Water absorbent composition |
| EP3280780B1 (en) * | 2015-04-06 | 2023-10-11 | UPL Limited | Water absorbent composition |
| US20230225909A1 (en) * | 2020-06-16 | 2023-07-20 | Afterclean Inc. | Vaginal fluid absorption and odor reduction |
| US20250186267A1 (en) * | 2020-06-16 | 2025-06-12 | Liviwell Inc. | Vaginal fluid absorption and odor reduction |
| US12447064B2 (en) * | 2020-06-16 | 2025-10-21 | Liviwell Inc. | Vaginal fluid absorption and odor reduction |
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Also Published As
| Publication number | Publication date |
|---|---|
| DE3128100A1 (de) | 1983-01-27 |
| DE3128100C2 (de) | 1986-05-22 |
| JPS58501107A (ja) | 1983-07-14 |
| US4693713A (en) | 1987-09-15 |
| EP0071063B1 (de) | 1985-12-11 |
| DE3267907D1 (en) | 1986-01-23 |
| JPH0581263B2 (cg-RX-API-DMAC7.html) | 1993-11-12 |
| WO1983000289A1 (fr) | 1983-02-03 |
| EP0071063A1 (de) | 1983-02-09 |
| ATE16891T1 (de) | 1985-12-15 |
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