Synthesis and Anticoagulant Activity of Sodium Alginate Sulfates
Editor(s)
Kennedy, J. F.and Mitchell, J. R.
Abstract
Sodium alginate sulfates prepared from sodium alginate through reaction with an uncommon sulfating agent (N (SO₃Na)₃) which was synthesized by sodium bisulfite and sodium nitrite in aqueous solution. the factors that could affect the degree of substitution (DS) of sodium alginate sulfates were investigated in detail. a sodium alginate sulfate with DS of 1.87 was obtained under optimal conditions. the structures of the derivatives were characterized by FTIR and ¹³C NMR. FTIR spectra showed the characteristic absorptions of sulfate ester bonds at 1249 cmˉ¹ and 873 cmˉ¹. the in vitro coagulation assay of human plasma containing the sodium alginate sulfates was determined with respect to activated partial thromboplastin time (APTT), thrombin time (TT) and prothombin time (PT). These activities strongly depended on the DS, molecular weight (M[subscript w]) and the concentration of sodium alginate sulfates. the introduction of sulfate groups to hydroxyl groups greatly prolonged the APTT and TT. Low S% and concentration sodium alginate sulfates showed little anticoagulant activity. the high DS and concentration could inhibit the activity of IIa and Xa to prolong APTT and TT. the low molecular weight resulted in higher anti-factor Xa activity to promote anticoagulant activity. Generally, the introducing of sulfate groups could not increase PT, it had little effect on coagulation factors in the extrinsic pathway.
Recommended Citation
L. Fan et al., "Synthesis and Anticoagulant Activity of Sodium Alginate Sulfates," Carbohydrate Polymers, Elsevier, Jan 2011.
The definitive version is available at https://doi.org/10.1016/j.carbpol.2010.10.038
Department(s)
Mechanical and Aerospace Engineering
Keywords and Phrases
Sodium Alginate Sulfates; Sulfating Agent; Degree of Substitution; Molecular Weight; Anticoagulant Activity
International Standard Serial Number (ISSN)
0144-8617
Document Type
Article - Journal
Document Version
Citation
File Type
text
Language(s)
English
Rights
© 2011 Elsevier, All rights reserved.
Publication Date
01 Jan 2011