CA2364687C - Organ arrest, protection and preservation - Google Patents
Organ arrest, protection and preservation Download PDFInfo
- Publication number
- CA2364687C CA2364687C CA2364687A CA2364687A CA2364687C CA 2364687 C CA2364687 C CA 2364687C CA 2364687 A CA2364687 A CA 2364687A CA 2364687 A CA2364687 A CA 2364687A CA 2364687 C CA2364687 C CA 2364687C
- Authority
- CA
- Canada
- Prior art keywords
- adenosine
- composition
- local anaesthetic
- organ
- heart
- 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 - Fee Related
Links
- 210000000056 organ Anatomy 0.000 title claims abstract description 56
- 230000004224 protection Effects 0.000 title description 9
- 238000004321 preservation Methods 0.000 title description 2
- 239000000203 mixture Substances 0.000 claims abstract description 72
- 230000003444 anaesthetic effect Effects 0.000 claims abstract description 55
- 239000000556 agonist Substances 0.000 claims abstract description 34
- 239000004036 potassium channel stimulating agent Substances 0.000 claims abstract description 34
- 239000003379 purinergic P1 receptor agonist Substances 0.000 claims abstract description 34
- 229940122614 Adenosine receptor agonist Drugs 0.000 claims abstract description 33
- 238000000034 method Methods 0.000 claims abstract description 21
- OIRDTQYFTABQOQ-KQYNXXCUSA-N adenosine Chemical compound C1=NC=2C(N)=NC=NC=2N1[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O OIRDTQYFTABQOQ-KQYNXXCUSA-N 0.000 claims description 198
- 210000002216 heart Anatomy 0.000 claims description 161
- 239000002126 C01EB10 - Adenosine Substances 0.000 claims description 99
- 229960005305 adenosine Drugs 0.000 claims description 99
- 229960004194 lidocaine Drugs 0.000 claims description 85
- 239000000243 solution Substances 0.000 claims description 85
- NNJVILVZKWQKPM-UHFFFAOYSA-N Lidocaine Chemical compound CCN(CC)CC(=O)NC1=C(C)C=CC=C1C NNJVILVZKWQKPM-UHFFFAOYSA-N 0.000 claims description 84
- 239000011591 potassium Substances 0.000 claims description 45
- 229910052700 potassium Inorganic materials 0.000 claims description 45
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims description 44
- 150000001875 compounds Chemical class 0.000 claims description 38
- 239000000546 pharmaceutical excipient Substances 0.000 claims description 26
- 239000003085 diluting agent Substances 0.000 claims description 25
- 239000002671 adjuvant Substances 0.000 claims description 24
- 239000003814 drug Substances 0.000 claims description 18
- 208000010125 myocardial infarction Diseases 0.000 claims description 13
- 210000004369 blood Anatomy 0.000 claims description 12
- 239000008280 blood Substances 0.000 claims description 12
- 238000004519 manufacturing process Methods 0.000 claims description 9
- 108091006146 Channels Proteins 0.000 claims description 7
- 239000000872 buffer Substances 0.000 claims description 7
- -1 pinicadil Chemical compound 0.000 claims description 7
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 claims description 6
- 230000002526 effect on cardiovascular system Effects 0.000 claims description 6
- 239000011777 magnesium Substances 0.000 claims description 6
- 229910052749 magnesium Inorganic materials 0.000 claims description 6
- MVFGUOIZUNYYSO-UHFFFAOYSA-N prilocaine Chemical compound CCCNC(C)C(=O)NC1=CC=CC=C1C MVFGUOIZUNYYSO-UHFFFAOYSA-N 0.000 claims description 6
- 229960001807 prilocaine Drugs 0.000 claims description 6
- MFDFERRIHVXMIY-UHFFFAOYSA-N procaine Chemical compound CCN(CC)CCOC(=O)C1=CC=C(N)C=C1 MFDFERRIHVXMIY-UHFFFAOYSA-N 0.000 claims description 6
- 229960004919 procaine Drugs 0.000 claims description 6
- 230000001101 cardioplegic effect Effects 0.000 claims description 5
- 239000003112 inhibitor Substances 0.000 claims description 5
- CHMUHOFITZIING-XNIJJKJLSA-N (2r,3r,4s,5r)-2-(6-aminopurin-9-yl)-2-cyclohexyl-5-(hydroxymethyl)oxolane-3,4-diol Chemical compound C1=NC=2C(N)=NC=NC=2N1[C@]1(C2CCCCC2)O[C@H](CO)[C@@H](O)[C@H]1O CHMUHOFITZIING-XNIJJKJLSA-N 0.000 claims description 4
- JADDQZYHOWSFJD-FLNNQWSLSA-N N-ethyl-5'-carboxamidoadenosine Chemical compound O[C@@H]1[C@H](O)[C@@H](C(=O)NCC)O[C@H]1N1C2=NC=NC(N)=C2N=C1 JADDQZYHOWSFJD-FLNNQWSLSA-N 0.000 claims description 4
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- IZEKFCXSFNUWAM-UHFFFAOYSA-N dipyridamole Chemical group C=12N=C(N(CCO)CCO)N=C(N3CCCCC3)C2=NC(N(CCO)CCO)=NC=1N1CCCCC1 IZEKFCXSFNUWAM-UHFFFAOYSA-N 0.000 claims description 4
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- GKEMHVLBZNVZOI-SJKOYZFVSA-N (1r,2r)-n-methyl-1-oxo-2-pyridin-3-ylthiane-2-carbothioamide Chemical compound C=1C=CN=CC=1[C@@]1(C(=S)NC)CCCC[S@]1=O GKEMHVLBZNVZOI-SJKOYZFVSA-N 0.000 claims description 3
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- SGTNSNPWRIOYBX-UHFFFAOYSA-N 2-(3,4-dimethoxyphenyl)-5-{[2-(3,4-dimethoxyphenyl)ethyl](methyl)amino}-2-(propan-2-yl)pentanenitrile Chemical compound C1=C(OC)C(OC)=CC=C1CCN(C)CCCC(C#N)(C(C)C)C1=CC=C(OC)C(OC)=C1 SGTNSNPWRIOYBX-UHFFFAOYSA-N 0.000 claims description 3
- KAWIOCMUARENDQ-UHFFFAOYSA-N 2-(4-chlorophenyl)sulfanyl-n-(4-pyridin-2-yl-1,3-thiazol-2-yl)acetamide Chemical compound C1=CC(Cl)=CC=C1SCC(=O)NC1=NC(C=2N=CC=CC=2)=CS1 KAWIOCMUARENDQ-UHFFFAOYSA-N 0.000 claims description 3
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- SQMWSBKSHWARHU-SDBHATRESA-N n6-cyclopentyladenosine Chemical compound O[C@@H]1[C@H](O)[C@@H](CO)O[C@H]1N1C2=NC=NC(NC3CCCC3)=C2N=C1 SQMWSBKSHWARHU-SDBHATRESA-N 0.000 claims description 3
- LBHIOVVIQHSOQN-UHFFFAOYSA-N nicorandil Chemical compound [O-][N+](=O)OCCNC(=O)C1=CC=CN=C1 LBHIOVVIQHSOQN-UHFFFAOYSA-N 0.000 claims description 3
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- JWZZKOKVBUJMES-UHFFFAOYSA-N (+-)-Isoprenaline Chemical compound CC(C)NCC(O)C1=CC=C(O)C(O)=C1 JWZZKOKVBUJMES-UHFFFAOYSA-N 0.000 claims description 2
- HMJIYCCIJYRONP-UHFFFAOYSA-N (+-)-Isradipine Chemical compound COC(=O)C1=C(C)NC(C)=C(C(=O)OC(C)C)C1C1=CC=CC2=NON=C12 HMJIYCCIJYRONP-UHFFFAOYSA-N 0.000 claims description 2
- RIRGCFBBHQEQQH-SSFGXONLSA-N (-)-n6-(2-phenylisopropyl)adenosine Chemical compound C([C@@H](C)NC=1C=2N=CN(C=2N=CN=1)[C@H]1[C@@H]([C@H](O)[C@@H](CO)O1)O)C1=CC=CC=C1 RIRGCFBBHQEQQH-SSFGXONLSA-N 0.000 claims description 2
- BIXYYZIIJIXVFW-UUOKFMHZSA-N (2R,3R,4S,5R)-2-(6-amino-2-chloro-9-purinyl)-5-(hydroxymethyl)oxolane-3,4-diol Chemical compound C1=NC=2C(N)=NC(Cl)=NC=2N1[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O BIXYYZIIJIXVFW-UUOKFMHZSA-N 0.000 claims description 2
- GTSCNQPMGNAJSH-YHFCJVPQSA-N (2S)-2-[[(2S)-2-[[(4R,7S,10S,16S,19R)-19-[[(3S,6S,9S,12S,15S,21R,26R,29S,32S,35S,38S,41S)-21-[[2-[[(1R,2aR,4S,7S,9aS,10S,12aS,13S,15aS,16S,18aS,19S,22S,25S,28S,31S,34S,37S,40S,43S,46S,52R,57R,60S,63S,66S,69S,72S,75S,81S,84S,87S,90S,93S,96S,99S)-7,63,90-tris(4-aminobutyl)-2a-[[(2S,3S)-2-[[(2S)-2-amino-5-carbamimidamidopentanoyl]amino]-3-methylpentanoyl]amino]-12a-(2-amino-2-oxoethyl)-25-(3-amino-3-oxopropyl)-13-benzyl-16,37,96-tris[(2S)-butan-2-yl]-19,28,46,72-tetrakis(3-carbamimidamidopropyl)-15a,31,43-tris(2-carboxyethyl)-9a,22,60,66-tetrakis[(1R)-1-hydroxyethyl]-40,84-bis(hydroxymethyl)-4,34,99-tris[(4-hydroxyphenyl)methyl]-93-(1H-imidazol-5-ylmethyl)-69,87-dimethyl-81-(2-methylpropyl)-10-(2-methylsulfanylethyl)-1a,2,5,8,8a,11,11a,14,14a,17,17a,20,20a,23,26,29,32,35,38,41,44,47,50,59,62,65,68,71,74,80,83,86,89,92,95,98-hexatriacontaoxo-18a-propan-2-yl-4a,5a,54,55-tetrathia-a,3,6,7a,9,10a,12,13a,15,16a,18,19a,21,24,27,30,33,36,39,42,45,48,51,58,61,64,67,70,73,79,82,85,88,91,94,97-hexatriacontazatricyclo[55.49.14.075,79]icosahectane-52-carbonyl]amino]acetyl]amino]-35-(3-amino-3-oxopropyl)-29-(2-carboxyethyl)-12,32-bis[(1R)-1-hydroxyethyl]-38-[(4-hydroxyphenyl)methyl]-3-(1H-indol-3-ylmethyl)-9-methyl-6-(2-methylsulfanylethyl)-2,5,8,11,14,20,28,31,34,37,40-undecaoxo-23,24-dithia-1,4,7,10,13,19,27,30,33,36,39-undecazatricyclo[39.3.0.015,19]tetratetracontane-26-carbonyl]amino]-16-(4-aminobutyl)-7-(3-carbamimidamidopropyl)-10-(carboxymethyl)-6,9,12,15,18-pentaoxo-1,2-dithia-5,8,11,14,17-pentazacycloicosane-4-carbonyl]amino]-4-amino-4-oxobutanoyl]amino]-6-aminohexanoic acid Chemical compound CC[C@H](C)[C@H](NC(=O)[C@@H](N)CCCNC(N)=N)C(=O)N[C@H]1CSSC[C@@H]2NC(=O)[C@@H](NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CCC(O)=O)NC(=O)[C@@H](NC(=O)[C@H](CSSC[C@H](NC(=O)CNC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@H](Cc3ccc(O)cc3)NC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@@H](NC(=O)[C@H](Cc3ccccc3)NC(=O)[C@H](CCSC)NC(=O)[C@H](CCCCN)NC(=O)[C@H](Cc3ccc(O)cc3)NC2=O)[C@@H](C)CC)[C@@H](C)O)[C@@H](C)CC)C(=O)NCC(=O)N[C@H]2CSSC[C@H](NC(=O)[C@H](CCC(O)=O)NC(=O)[C@@H](NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](Cc3ccc(O)cc3)NC(=O)[C@@H]3CCCN3C(=O)[C@H](Cc3c[nH]c4ccccc34)NC(=O)[C@H](CCSC)NC(=O)[C@H](C)NC(=O)[C@@H](NC(=O)[C@@H]3CCCN3C2=O)[C@@H](C)O)[C@@H](C)O)C(=O)N[C@H]2CSSC[C@H](NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CC(O)=O)NC(=O)CNC(=O)[C@H](CCCCN)NC2=O)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CCCCN)C(O)=O)NC(=O)[C@@H](NC(=O)[C@H](CCCCN)NC(=O)[C@@H](NC(=O)[C@H](C)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@@H]2CCCN2C(=O)[C@H](CC(C)C)NC(=O)[C@H](CO)NC(=O)[C@H](C)NC(=O)[C@H](CCCCN)NC(=O)[C@H](Cc2cnc[nH]2)NC(=O)[C@@H](NC(=O)[C@H](Cc2ccc(O)cc2)NC1=O)[C@@H](C)CC)[C@@H](C)O)[C@@H](C)O)C(C)C)[C@@H](C)O GTSCNQPMGNAJSH-YHFCJVPQSA-N 0.000 claims description 2
- VLPIATFUUWWMKC-SNVBAGLBSA-N (2r)-1-(2,6-dimethylphenoxy)propan-2-amine Chemical compound C[C@@H](N)COC1=C(C)C=CC=C1C VLPIATFUUWWMKC-SNVBAGLBSA-N 0.000 claims description 2
- ZHWHMUIGIKPSJN-WOUKDFQISA-N (2r,3r,4s,5r)-2-(6-aminopurin-9-yl)-2-ethyl-5-(hydroxymethyl)oxolane-3,4-diol Chemical compound C1=NC2=C(N)N=CN=C2N1[C@]1(CC)O[C@H](CO)[C@@H](O)[C@H]1O ZHWHMUIGIKPSJN-WOUKDFQISA-N 0.000 claims description 2
- PVHUJELLJLJGLN-INIZCTEOSA-N (S)-nitrendipine Chemical compound CCOC(=O)C1=C(C)NC(C)=C(C(=O)OC)[C@@H]1C1=CC=CC([N+]([O-])=O)=C1 PVHUJELLJLJGLN-INIZCTEOSA-N 0.000 claims description 2
- FQUYSHZXSKYCSY-UHFFFAOYSA-N 1,4-diazepane Chemical compound C1CNCCNC1 FQUYSHZXSKYCSY-UHFFFAOYSA-N 0.000 claims description 2
- FHVUTHWUIUXZBY-QLANQDRJSA-N 147794-23-8 Chemical compound C([C@H]1C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H]2C(=O)N[C@@H]3C(=O)N[C@@H](CO)C(=O)NCC(=O)N[C@@H](CO)C(=O)N[C@H](C(NCC(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CCCNC(N)=N)C(=O)NCC(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CSSC2)C(N)=O)=O)CSSC[C@H](NC(=O)[C@@H]2CCCN2C(=O)[C@H](C)NC(=O)CNC(=O)[C@H](CCCCN)NC(=O)CNC(=O)[C@H](CCCCN)NC(=O)[C@@H](N)CSSC3)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CCCCN)C(=O)N[C@H](C(=O)N[C@H](C(N1)=O)CCSC)[C@@H](C)O)C1=CC=C(O)C=C1 FHVUTHWUIUXZBY-QLANQDRJSA-N 0.000 claims description 2
- UIAGMCDKSXEBJQ-IBGZPJMESA-N 3-o-(2-methoxyethyl) 5-o-propan-2-yl (4s)-2,6-dimethyl-4-(3-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylate Chemical compound COCCOC(=O)C1=C(C)NC(C)=C(C(=O)OC(C)C)[C@H]1C1=CC=CC([N+]([O-])=O)=C1 UIAGMCDKSXEBJQ-IBGZPJMESA-N 0.000 claims description 2
- QOYHHIBFXOOADH-UHFFFAOYSA-N 8-[4,4-bis(4-fluorophenyl)butyl]-1-phenyl-1,3,8-triazaspiro[4.5]decan-4-one Chemical compound C1=CC(F)=CC=C1C(C=1C=CC(F)=CC=1)CCCN1CCC2(C(NCN2C=2C=CC=CC=2)=O)CC1 QOYHHIBFXOOADH-UHFFFAOYSA-N 0.000 claims description 2
- PAOANWZGLPPROA-RQXXJAGISA-N CGS-21680 Chemical compound O[C@@H]1[C@H](O)[C@@H](C(=O)NCC)O[C@H]1N1C2=NC(NCCC=3C=CC(CCC(O)=O)=CC=3)=NC(N)=C2N=C1 PAOANWZGLPPROA-RQXXJAGISA-N 0.000 claims description 2
- 101000723297 Dendroaspis polylepis polylepis Calciseptin Proteins 0.000 claims description 2
- XQLWNAFCTODIRK-UHFFFAOYSA-N Gallopamil Chemical compound C1=C(OC)C(OC)=CC=C1CCN(C)CCCC(C#N)(C(C)C)C1=CC(OC)=C(OC)C(OC)=C1 XQLWNAFCTODIRK-UHFFFAOYSA-N 0.000 claims description 2
- ZFMITUMMTDLWHR-UHFFFAOYSA-N Minoxidil Chemical compound NC1=[N+]([O-])C(N)=CC(N2CCCCC2)=N1 ZFMITUMMTDLWHR-UHFFFAOYSA-N 0.000 claims description 2
- ZBBHBTPTTSWHBA-UHFFFAOYSA-N Nicardipine Chemical compound COC(=O)C1=C(C)NC(C)=C(C(=O)OCCN(C)CC=2C=CC=CC=2)C1C1=CC=CC([N+]([O-])=O)=C1 ZBBHBTPTTSWHBA-UHFFFAOYSA-N 0.000 claims description 2
- CXOFVDLJLONNDW-UHFFFAOYSA-N Phenytoin Chemical compound N1C(=O)NC(=O)C1(C=1C=CC=CC=1)C1=CC=CC=C1 CXOFVDLJLONNDW-UHFFFAOYSA-N 0.000 claims description 2
- 229930001406 Ryanodine Natural products 0.000 claims description 2
- ZUSWDTWYONAOPH-UHFFFAOYSA-N [2-(trifluoromethyl)phenyl]hydrazine;hydrochloride Chemical group [Cl-].[NH3+]NC1=CC=CC=C1C(F)(F)F ZUSWDTWYONAOPH-UHFFFAOYSA-N 0.000 claims description 2
- 229960000643 adenine Drugs 0.000 claims description 2
- HTIQEAQVCYTUBX-UHFFFAOYSA-N amlodipine Chemical compound CCOC(=O)C1=C(COCCN)NC(C)=C(C(=O)OC)C1C1=CC=CC=C1Cl HTIQEAQVCYTUBX-UHFFFAOYSA-N 0.000 claims description 2
- 229960000528 amlodipine Drugs 0.000 claims description 2
- GOOXRYWLNNXLFL-UHFFFAOYSA-H azane oxygen(2-) ruthenium(3+) ruthenium(4+) hexachloride Chemical compound N.N.N.N.N.N.N.N.N.N.N.N.N.N.[O--].[O--].[Cl-].[Cl-].[Cl-].[Cl-].[Cl-].[Cl-].[Ru+3].[Ru+3].[Ru+4] GOOXRYWLNNXLFL-UHFFFAOYSA-H 0.000 claims description 2
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- ZFLWDHHVRRZMEI-UHFFFAOYSA-N methyl 2,6-dimethyl-5-nitro-4-[2-(trifluoromethyl)phenyl]-1,4-dihydropyridine-3-carboxylate Chemical compound COC(=O)C1=C(C)NC(C)=C([N+]([O-])=O)C1C1=CC=CC=C1C(F)(F)F ZFLWDHHVRRZMEI-UHFFFAOYSA-N 0.000 claims description 2
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| AUPQ4199A AUPQ419999A0 (en) | 1999-11-23 | 1999-11-23 | Organ arrest, protection and preservation |
| AUPQ4199 | 1999-11-23 | ||
| PCT/AU2000/000226 WO2000056145A1 (en) | 1999-03-23 | 2000-03-22 | Organ arrest, protection and preservation |
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| US20040170950A1 (en) * | 2002-09-12 | 2004-09-02 | Prien Samuel D. | Organ preservation apparatus and methods |
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| AU2003291847B2 (en) * | 2002-12-23 | 2010-12-02 | Hibernation Therapeutics, A Kf Llc | Organ preconditioning, arrest, protection, preservation and recovery |
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| SG173404A1 (en) * | 2006-07-25 | 2011-08-29 | Hibernation Therapeutics Ltd | Trauma therapy |
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| EP2219442A4 (en) * | 2007-07-25 | 2012-05-02 | Hibernation Therapeutics Ltd | IMPROVED ORGAN PROTECTION, IMPROVED ORGAN CONSERVATION AND IMPROVED ORGAN RECOVERY |
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| US20090185973A1 (en) * | 2008-01-22 | 2009-07-23 | Adenobio N.V. | Methods, compositions, unit dosage forms, and kits for pharmacologic stress testing with reduced side effects |
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| EP2908858B1 (en) | 2012-10-19 | 2020-06-24 | New York University | Compositions for use in inhibiting osteolysis |
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| JP2013234200A (ja) * | 2013-08-19 | 2013-11-21 | Hibernation Therapeutics Ltd | 組織維持の改善 |
| US10092591B2 (en) | 2014-02-27 | 2018-10-09 | University Of Alaska Fairbanks | Methods and compositions for the treatment of ischemic injury to tissue using therapeutic hypothermia |
| CN103893205B (zh) * | 2014-04-15 | 2016-03-09 | 青岛大学附属医院 | 一种包含利多卡因和腺苷的心脏停搏液及其制备方法 |
| US20170049811A1 (en) * | 2014-05-01 | 2017-02-23 | Catherine E. Berry | Modified single dose, microplegic approach to cardioplegia for adult heart |
| US9501418B2 (en) * | 2014-06-26 | 2016-11-22 | HGST Netherlands B.V. | Invalidation data area for cache |
| US9913903B2 (en) * | 2015-08-06 | 2018-03-13 | Grifols Worldwide Operations Limited | Method for the treatment or prevention of infection-related immune conditions using a composition comprising IgM |
| CN109769797B (zh) * | 2017-11-13 | 2024-09-10 | 合肥华琪生物工程有限公司 | 一种器官保存液 |
| US12471592B2 (en) | 2021-08-18 | 2025-11-18 | Reelabs Private Limited | Cytoprotective compositions for short-term cells storage and transportation without cryopreservation and deep freezing |
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| CA2717162A1 (en) | 2007-03-02 | 2008-09-12 | Hibernation Therapeutics Limited | Transplants |
| CN100423638C (zh) | 2007-03-22 | 2008-10-08 | 南京吉脉生物技术有限公司 | 一种器官保存液及其制备方法 |
| EP2219442A4 (en) | 2007-07-25 | 2012-05-02 | Hibernation Therapeutics Ltd | IMPROVED ORGAN PROTECTION, IMPROVED ORGAN CONSERVATION AND IMPROVED ORGAN RECOVERY |
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2000
- 2000-03-22 CN CN00805408A patent/CN1344135A/zh active Pending
- 2000-03-22 KR KR1020017012071A patent/KR20020001797A/ko not_active Withdrawn
- 2000-03-22 DE DE60034778T patent/DE60034778T2/de not_active Expired - Lifetime
- 2000-03-22 WO PCT/AU2000/000226 patent/WO2000056145A1/en not_active Ceased
- 2000-03-22 EP EP10181888.8A patent/EP2359688B1/en not_active Expired - Lifetime
- 2000-03-22 CA CA2364687A patent/CA2364687C/en not_active Expired - Fee Related
- 2000-03-22 EP EP00910414A patent/EP1168912B1/en not_active Expired - Lifetime
- 2000-03-22 NZ NZ514515A patent/NZ514515A/en not_active IP Right Cessation
- 2000-03-22 EP EP06077320A patent/EP1790223A1/en not_active Withdrawn
- 2000-03-22 JP JP2000606063A patent/JP4949558B2/ja not_active Expired - Fee Related
- 2000-03-22 PL PL00351484A patent/PL351484A1/xx not_active Application Discontinuation
- 2000-03-22 MX MXPA01009552A patent/MXPA01009552A/es unknown
- 2000-03-22 IL IL14555200A patent/IL145552A0/xx unknown
- 2000-03-22 BR BR0010653-4A patent/BR0010653A/pt not_active Application Discontinuation
- 2000-03-22 AT AT00910414T patent/ATE361667T1/de not_active IP Right Cessation
- 2000-03-22 ES ES00910414T patent/ES2287001T3/es not_active Expired - Lifetime
- 2000-03-22 US US09/937,181 patent/US6955814B1/en not_active Expired - Lifetime
- 2000-03-22 TR TR2001/03235T patent/TR200103235T2/xx unknown
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2001
- 2001-09-19 NO NO20014557A patent/NO331669B1/no not_active IP Right Cessation
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2005
- 2005-02-01 US US11/046,866 patent/US7223413B2/en not_active Expired - Fee Related
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2007
- 2007-04-24 US US11/790,216 patent/US20070270372A1/en not_active Abandoned
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2009
- 2009-08-13 US US12/541,000 patent/US7749522B2/en not_active Expired - Fee Related
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2010
- 2010-05-27 US US12/788,864 patent/US20100298254A1/en not_active Abandoned
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2011
- 2011-06-03 NO NO20110807A patent/NO20110807L/no not_active Application Discontinuation
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2013
- 2013-03-05 US US13/786,041 patent/US9320753B2/en not_active Expired - Fee Related
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2016
- 2016-03-18 US US15/074,471 patent/US20160263141A1/en not_active Abandoned
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