Beena M S, Chandy T, Sharma C P
Biosurface Technology Division, Sree Chitra Tirunal Institute for Medical Sciences and Technology, Trivandrum, India.
Artif Cells Blood Substit Immobil Biotechnol. 1995;23(2):175-92. doi: 10.3109/10731199509117937.
This work deals with the synthesis and blood compatibility studies of Heparin immobilized chitosan--polyethyleneglycol (Chit-PEG) hydrogels for various biomedical applications. Chit-PEG interpenetrating net work (IPN) had been synthesised by crosslinking different ratios of chitosan with glutaraldehyde using schiffs base reaction mechanism and interpenetrating polyethyleneglycol (PEG) to form hydrogen bonding between the amino hydrogen in chitosan and polyether oxygen. An optimum gel combination was selected from the IPN of Chit-PEG and used for bonding heparin. This modified gel had dramatically improved its blood compatibility. The antithrombotic function of this gel and the release profile of heparin had been investigated using coagulation assays, and spectrophotometric quantitation. Recalcification times of plasma exposed to heparin immobilized Chit-PEG hydrogel were markedly increased as compared to heparin free gels. The anticoagulant function of this gel matrix may be due to partially released heparin and bonded heparin.
本研究致力于肝素固定化壳聚糖 - 聚乙二醇(Chit - PEG)水凝胶的合成及其血液相容性研究,以用于各种生物医学应用。Chit - PEG互穿网络(IPN)是通过席夫碱反应机制,使不同比例的壳聚糖与戊二醛交联,并与互穿的聚乙二醇(PEG)形成氢键,该氢键存在于壳聚糖中的氨基氢与聚醚氧之间而合成的。从Chit - PEG的IPN中选择了最佳凝胶组合,并用于结合肝素。这种改性凝胶显著改善了其血液相容性。使用凝血测定法和分光光度法定量研究了该凝胶的抗血栓形成功能以及肝素的释放曲线。与不含肝素的凝胶相比,暴露于肝素固定化Chit - PEG水凝胶的血浆再钙化时间显著增加。这种凝胶基质的抗凝功能可能归因于部分释放的肝素和结合的肝素。