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添加不稳定明胶成分对稳定的聚乙二醇水凝胶降解及溶质释放动力学的影响

Effect of the addition of a labile gelatin component on the degradation and solute release kinetics of a stable PEG hydrogel.

作者信息

Waldeck H, Kao W J

机构信息

a Department of Biomedical Engineering , College of Engineering, University of Wisconsin-Madison , 777 Highland Avenue , Madison , WI , 53705 , USA.

出版信息

J Biomater Sci Polym Ed. 2012;23(12):1595-611. doi: 10.1163/092050611X587547. Epub 2012 May 11.

Abstract

Characterization of the degradation mechanisms and resulting products of biodegradable materials is critical in understanding the behavior of the material including solute transport and biological response. Previous mathematical analyses of a semi-interpenetrating network (sIPN) containing both labile gelatin and a stable cross-linked poly(ethylene glycol) (PEG) network found that diffusion-based models alone were unable to explain the release kinetics of solutes from the system. In this study, degradation of the sIPN and its effect on solute release and swelling kinetics were investigated. The kinetics of the primary mode of degradation, gelatin dissolution, was dependent on temperature, preparation methods, PEGdA and gelatin concentration, and the weight ratio between the gelatin and PEG. The gelatin dissolution rate positively correlated with both matrix swelling and the release kinetics of high-molecular-weight model compound, FITC-dextran. Coupled with previous in vitro studies, the kinetics of sIPN degradation provided insights into the time-dependent changes in cellular response including adhesion and protein expression. These results provide a facile guide in material formulation to control the delivery of high-molecular-weight compounds with concomitant modulation of cellular behavior.

摘要

对可生物降解材料的降解机制及降解产物进行表征,对于理解材料的行为(包括溶质传输和生物反应)至关重要。先前对包含不稳定明胶和稳定交联聚乙二醇(PEG)网络的半互穿网络(sIPN)进行的数学分析发现,仅基于扩散的模型无法解释溶质从该系统中的释放动力学。在本研究中,对sIPN的降解及其对溶质释放和溶胀动力学的影响进行了研究。主要降解模式(明胶溶解)的动力学取决于温度、制备方法、聚乙二醇二丙烯酸酯(PEGdA)和明胶浓度,以及明胶与PEG之间的重量比。明胶溶解速率与基质溶胀和高分子量模型化合物异硫氰酸荧光素 - 葡聚糖(FITC - dextran)的释放动力学均呈正相关。结合先前的体外研究,sIPN降解动力学为包括细胞黏附与蛋白质表达在内的细胞反应随时间的变化提供了见解。这些结果为材料配方提供了简便的指导,以控制高分子量化合物的递送并同时调节细胞行为。

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