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Removal of the anticoagulant activities of the low molecular weight heparin fractions and fragments with flavobacterial heparinase

dc.contributor.authorYang, Victor C.en_US
dc.contributor.authorBernstein, Howarden_US
dc.contributor.authorCooney, Charles L.en_US
dc.contributor.authorKadam, Jill C.en_US
dc.contributor.authorLanger, Robert S.en_US
dc.date.accessioned2006-04-07T19:23:25Z
dc.date.available2006-04-07T19:23:25Z
dc.date.issued1986-12-01en_US
dc.identifier.citationYang, Victor C., Bernstein, Howard, Cooney, Charles L., Kadam, Jill C., Langer, Robert (1986/12/01)."Removal of the anticoagulant activities of the low molecular weight heparin fractions and fragments with flavobacterial heparinase." Thrombosis Research 44(5): 599-610. <http://hdl.handle.net/2027.42/25962>en_US
dc.identifier.urihttp://www.sciencedirect.com/science/article/B6T1C-4C2RTHW-B9/2/f5800760b074a77d030d68e7f13bc1been_US
dc.identifier.urihttps://hdl.handle.net/2027.42/25962
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=3810562&dopt=citationen_US
dc.description.abstractRecently, the development of low molecular weight heparin fractions and fragments. (LMHF) as potential anti-thrombotic agents has gained increased attention. However, the lack of antagonists to neutralize the anti-coagulant effects of these drugs may seriously exclude them from possible uses in extracorporeal therapy. This is mainly because of the concern that the high dosage of the drugs employed in extracorporeal therapy could lead to serious bleeding risks. Our earlier work has demonstrated that immobilized heparinase can remove polydis-perse heparin both and . To examine whether such a system may be used as a novel approach to neutralize the anticoagulant effects of LMHF, different LMMF were tested using heparinase. data showed that both the APTT and anti-FXa activities of the LMHF including Kabi 2165, PK 10169, CY 216 and CY 222 were nearly completely eliminated by heparinase in less than 20 min. This study suggests that an immobilized heparinase system may be an useful element for the acceptance of the LMHF for their use in extracorporeal, therapy.en_US
dc.format.extent991537 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherElsevieren_US
dc.titleRemoval of the anticoagulant activities of the low molecular weight heparin fractions and fragments with flavobacterial heparinaseen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelInternal Medicine and Specialtiesen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumCurrent address: College of Pharmacy, The University of Michigan, Ann Arbor, Michigan 48109, USA: Department of Applied Biological Sciences, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139, USAen_US
dc.contributor.affiliationotherDepartment of Chemical Engineering, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139, USA: Department of Applied Biological Sciences, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139, USAen_US
dc.contributor.affiliationotherDepartment of Chemical Engineering, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139, USA: Department of Applied Biological Sciences, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139, USAen_US
dc.contributor.affiliationotherDepartment of Applied Biological Sciences, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139, USAen_US
dc.contributor.affiliationotherDepartment of Surgery, Children's Hospital Medical Center, Boston, Massachusetts 02115, USA: Department of Applied Biological Sciences, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139, USAen_US
dc.identifier.pmid3810562en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/25962/1/0000028.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1016/0049-3848(86)90162-3en_US
dc.identifier.sourceThrombosis Researchen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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