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表面形态和电荷对藻酸盐/壳聚糖微胶囊上吸附的纤维蛋白原数量和构象的影响。

Effect of surface morphology and charge on the amount and conformation of fibrinogen adsorbed onto alginate/chitosan microcapsules.

机构信息

Laboratory of Biomedical Material Engineering, Biotechnology Division, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian 116023, People's Republic of China.

出版信息

Langmuir. 2010 Apr 20;26(8):5587-94. doi: 10.1021/la903874g.

Abstract

We report the influence of surface morphology and charge of alginate/chitosan (ACA) microcapsules on both the amount of adsorbed protein and its secondary structural changes during adsorption. Variations in surface morphology and charge were controlled by varying alginate molecular weight and chitosan concentration. Plasma fibrinogen (Fgn) was chosen to model this adsorption to foreign surfaces. The surface of ACA microcapsules exhibited a granular structure after incubating calcium alginate beads with chitosan solution to form membranes. The surface roughness of ACA microcapsule membranes decreased with decreasing alginate molecular weight and chitosan concentration. Zeta potential measurements showed that there was a net negative charge on the surface of ACA microcapsules which decreased with decreasing alginate molecular weight and chitosan concentration. The increase in both surface roughness and zeta potential resulted in an increase in the amount of Fgn adsorbed. Moreover, the higher the zeta potential was, the stronger the protein-surface interaction between fibrinogen and ACA microcapsules was. More protein molecules adsorbed spread and had a greater conformational change on rougher surfaces for more surfaces being available for protein to attach.

摘要

我们研究了海藻酸钠/壳聚糖(ACA)微胶囊的表面形态和电荷对吸附过程中吸附蛋白量及其二级结构变化的影响。通过改变海藻酸钠分子量和壳聚糖浓度来控制表面形态和电荷的变化。选择血浆纤维蛋白原(Fgn)来模拟这种对外来表面的吸附。用壳聚糖溶液孵育钙离子海藻酸钠珠形成膜后,ACA 微胶囊的表面呈现出颗粒状结构。ACA 微胶囊膜的表面粗糙度随海藻酸钠分子量和壳聚糖浓度的降低而降低。Zeta 电位测量表明,ACA 微胶囊表面带有净负电荷,随海藻酸钠分子量和壳聚糖浓度的降低而降低。表面粗糙度和 Zeta 电位的增加导致 Fgn 吸附量的增加。此外,Zeta 电位越高,纤维蛋白原与 ACA 微胶囊之间的蛋白-表面相互作用越强。更多的蛋白质分子吸附在更粗糙的表面上扩散,并发生更大的构象变化,因为有更多的表面可供蛋白质附着。

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