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细胞模拟单层支撑的壳聚糖血液相容性研究。

Cell mimetic monolayer supported chitosan-haemocompatibility studies.

作者信息

Mathews Smitha, Kaladhar K, Sharma Chandra P

机构信息

Division of Biosurface Technology, Biomedical Technology Wing, Sree Chitra Tirunal Institute for Medical Sciences and Technology, Thiruvananthapuram 695 012, Kerala, India.

出版信息

J Biomed Mater Res A. 2006 Oct;79(1):147-52. doi: 10.1002/jbm.a.30710.

Abstract

Chitosan is a natural polymer, widely explored for biomedical and tissue engineering applications. However the thrombogenic nature limits their application in blood contacting devices and implants. Here, we have attempted to understand the haemocompatibility of chitosan by immobilizing a monolayer of cell mimetic lipid compositions. The phosphatidylcholine/cholesterol/galactocerebroside lipid composition (PC/Chol/GalC, 1:0.35:0.125) was deposited onto the chitosan films. Characterization of the modified surface was done by sessile drop contact angle measurement. The contact angle of the chitosan film reduced from 80.65 +/- 1.4 to 23.5 +/- 1.9 after the surface modification. Swelling nature of chitosan seemed to influence the orientation and packing of the lipid monolayer. In vitro calcification studies with metastable salt solution indicated increased calcification on the modified surface. This may be due to formation of nuclei for calcification on the expanding monolayer. The preliminary haemocompatibility studies with washed platelets, leukocytes and erythrocytes showed overall reduction in blood cell adhesion to the modified surfaces. Scanning electron microscopy was used for morphological characterization of platelet adhesion and activation on the surfaces. On the bare chitosan surface, fully spread platelets with extending pseudopodia indicated platelet activation. The smooth surface of the modified film did not activate platelets. These studies showed that, though the lipid monolayer on chitosan film is able to reduce the over all blood cell adhesion and platelet activation it is prone to calcification.

摘要

壳聚糖是一种天然聚合物,在生物医学和组织工程应用方面得到了广泛研究。然而,其血栓形成特性限制了它们在血液接触装置和植入物中的应用。在此,我们试图通过固定一层细胞模拟脂质组合物来了解壳聚糖的血液相容性。将磷脂酰胆碱/胆固醇/半乳糖脑苷脂脂质组合物(PC/Chol/GalC,1:0.35:0.125)沉积在壳聚糖薄膜上。通过静滴接触角测量对改性表面进行表征。表面改性后,壳聚糖薄膜的接触角从80.65±1.4减小到23.5±1.9。壳聚糖的膨胀性质似乎影响脂质单层的取向和堆积。用亚稳盐溶液进行的体外钙化研究表明,改性表面的钙化增加。这可能是由于在膨胀的单层上形成了钙化核。用洗涤过的血小板、白细胞和红细胞进行的初步血液相容性研究表明,血细胞在改性表面的粘附总体减少。扫描电子显微镜用于表面血小板粘附和活化的形态学表征。在裸露的壳聚糖表面,带有延伸伪足的完全铺展的血小板表明血小板被激活。改性薄膜的光滑表面未激活血小板。这些研究表明,尽管壳聚糖薄膜上的脂质单层能够减少总体血细胞粘附和血小板活化,但它易于钙化。

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