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磷酸盐交联壳聚糖凝胶的微观结构与性能的相关性研究。

On the Correlation between the Microscopic Structure and Properties of Phosphate-Cross-Linked Chitosan Gels.

机构信息

Department of Life Sciences , University of Trieste , Via Licio Giorgieri 5 , I-34127 Trieste , Italy.

Department of Engineering and Architecture , University of Trieste , Via A. Valerio 6/1 , I-34127 Trieste , Italy.

出版信息

ACS Appl Mater Interfaces. 2018 Apr 4;10(13):10761-10770. doi: 10.1021/acsami.8b01834. Epub 2018 Mar 23.

DOI:10.1021/acsami.8b01834
PMID:29569895
Abstract

Ionic chitosan gels fabricated using multivalent anions, tripolyphosphate (TPP) or pyrophosphate (PPi), respectively, have been investigated as potential biomaterials to be used in tissue engineering. Starting from the hypothesis that the polymer mesh texture at the microscale affects the final performance of the resulting materials, an innovative image analysis approach is presented in the first part of the article, which is aimed at deriving quantitative information from transmission electron microscopy images. The image analysis of the (more extended) central area of the gel networks revealed differences between both the cross-linking densities and pore size distributions of the two systems, the TPP gels showing a higher connectivity. Chitosan-TPP gels showed a limited degradation in simulated physiological media up to 6 weeks, reasonably ascribed to the texture of the (more extended) central area of the gels, whereas PPi counterparts degraded almost immediately. The release profiles and the calculation of diffusion coefficients for bovine serum albumin and cytochrome c, herein used as model payloads, indicated a different release behavior depending on the polymer network homogeneity/inhomogeneity and molecular weight of loaded molecules. This finding was ascribed to the marked inhomogeneity of the PPi gels (at variance with the TPP ones), which had been demonstrated in our previous work. Finally, thorough in vitro studies demonstrated good biocompatibility of both chitosan gels, and because of this feature, they can be used as suitable scaffolds for cellular colonization and metabolic activity.

摘要

分别使用多价阴离子三聚磷酸酯(TPP)或焦磷酸酯(PPi)制备的壳聚糖离子凝胶已被研究作为组织工程中潜在的生物材料。从聚合物微观网状结构影响最终材料性能的假设出发,本文第一部分提出了一种创新的图像分析方法,旨在从透射电子显微镜图像中获取定量信息。对(更扩展的)凝胶网络中心区域的图像分析表明,两种体系的交联密度和孔径分布存在差异,TPP 凝胶的连接性更高。壳聚糖-TPP 凝胶在模拟生理介质中 6 周内的降解有限,这归因于凝胶(更扩展的)中心区域的结构,而 PPi 凝胶则几乎立即降解。牛血清白蛋白和细胞色素 c 的释放曲线和扩散系数的计算,本文中用作模型负载物,表明释放行为取决于聚合物网络的均一性/非均一性和负载分子的分子量。这一发现归因于 PPi 凝胶的明显不均匀性(与 TPP 凝胶不同),这在前一篇工作中已经得到证明。最后,全面的体外研究表明两种壳聚糖凝胶具有良好的生物相容性,因此它们可用作细胞定植和代谢活性的合适支架。

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