Analysis of the Action of Quaternized Chitosans with Different Molecular Weight on Anticoagulant Activity of Heparins In Vitro


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Quaternized derivatives of chitosan with a substitution degree of 85-98% (highly substituted) synthesized from chitosans with a molecular weight of 5, 10, 20 kDa, with a degree of deacetylation of 89-98%, and the code numbers of QChit 5, QChit 10, QChit 20, respectively, completely neutralize antithrombin activity of unfractionated heparin and partially neutralize aXa activity of low-molecular-weight heparin (clexane), similar to protamine sulfate. The advantages of QChit 5 and QChit 10 over QChit 20 and protamine sulphate are the follows: the effect is achieved at lower concentrations and in greater concentration range; they do not promote platelet aggregation; in a concentration of 0.0072 mg/ml they do not destroy the erythrocyte membranes.

Sobre autores

N. Drozd

National Medical Research Center of Hematology, Ministry of Health of the Russian Federation

Autor responsável pela correspondência
Email: nndrozd@mail.ru
Rússia, Moscow

Yu. Logvinova

National Medical Research Center of Hematology, Ministry of Health of the Russian Federation

Email: nndrozd@mail.ru
Rússia, Moscow

B. Shagdarova

Institute of Bioengineering, Fundamental Basics of Biotechnology, Russian Academy of Science

Email: nndrozd@mail.ru
Rússia, Moscow

A. Il’ina

Institute of Bioengineering, Fundamental Basics of Biotechnology, Russian Academy of Science

Email: nndrozd@mail.ru
Rússia, Moscow

V. Varlamov

Institute of Bioengineering, Fundamental Basics of Biotechnology, Russian Academy of Science

Email: nndrozd@mail.ru
Rússia, Moscow


Declaração de direitos autorais © Springer Science+Business Media, LLC, part of Springer Nature, 2019

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