| Literature DB >> 28878012 |
Yongmei Xu1, Kasemsiri Chandarajoti2,3, Xing Zhang4, Vijayakanth Pagadala1, Wenfang Dou1, Debra Moorman Hoppensteadt5, Erica M Sparkenbaugh2, Brian Cooley6, Sharon Daily7, Nigel S Key2, Diana Severynse-Stevens7, Jawed Fareed5, Robert J Linhardt8, Rafal Pawlinski9, Jian Liu10.
Abstract
Low-molecular weight heparin (LMWH) is used clinically to treat clotting disorders. As an animal-sourced product, LMWH is a highly heterogeneous mixture, and its anticoagulant activity is not fully reversible by protamine. Furthermore, the reliability of the LMWH supply chain is a concern for regulatory agencies. We demonstrate the synthesis of heparin dodecasaccharides (12-mers) at the gram scale. In vitro experiments demonstrate that the anticoagulant activity of the 12-mers could be reversed using protamine. One of these, labeled as 12-mer-1, reduced the size of blood clots in the mouse model of deep vein thrombosis and attenuated circulating procoagulant markers in the mouse model of sickle cell disease. An ex vivo experiment demonstrates that the anticoagulant activity of 12-mer-1 could be reversed by protamine. 12-mer-1 was also examined in a nonhuman primate model to determine its pharmacodynamic parameters. A 7-day toxicity study in a rat model showed no toxic effects. The data suggest that a synthetic homogeneous oligosaccharide can replace animal-sourced LMWHs.Entities:
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Year: 2017 PMID: 28878012 PMCID: PMC6231235 DOI: 10.1126/scitranslmed.aan5954
Source DB: PubMed Journal: Sci Transl Med ISSN: 1946-6234 Impact factor: 17.956