Watanabe J, Ooya T, Park K D, Kim Y H, Yui N
School of Materials Science, Japan Advanced Institute of Science and Technology, Tatsunokuchi, Ishikawa.
J Biomater Sci Polym Ed. 2000;11(12):1333-45. doi: 10.1163/156856200744363.
PEG hydrogels cross-linked by a hydrolyzable polyrotaxane were prepared and their hydrolytic erosion characterized in terms of supramolecular dissociation of the polyrotaxane. The hydrolyzable polyrotaxane, in which many alpha-cyclodextrins (alpha-CDs) are threaded onto a poly(ethylene glycol) (PEG) chain capped with L-phenylalanine via ester linkages, was used as a multifunctional cross-linker: the PEG network was covalently bound to hydroxyl groups of alpha-CDs in the polyrotaxane. The contact angle and water content of the hydrogels were varied with the polyrotaxane content in the feed. In vitro hydrolysis study revealed that the time to reach complete gel erosion was shortened by increasing the polyrotaxane content in the feed in relation to the decreased number of chemical cross-links between PEG and alpha-CDs in the polyrotaxane. The hydrogel degradation in a physiological condition was found to be followed by bulk mechanism. These findings suggest that changing the preparative conditions such as polyrotaxane content will make it possible to control programmed gel erosion for tissue engineering.
制备了由可水解聚轮烷交联的聚乙二醇水凝胶,并根据聚轮烷的超分子解离对其水解侵蚀进行了表征。可水解聚轮烷被用作多功能交联剂,其中许多α-环糊精(α-CD)通过酯键连接在由L-苯丙氨酸封端的聚乙二醇(PEG)链上:PEG网络与聚轮烷中α-CD的羟基共价结合。水凝胶的接触角和含水量随进料中聚轮烷含量的变化而变化。体外水解研究表明,相对于聚轮烷中PEG与α-CD之间化学交联数量的减少,通过增加进料中聚轮烷的含量,达到完全凝胶侵蚀的时间缩短。发现在生理条件下水凝胶的降解遵循整体机制。这些发现表明,改变诸如聚轮烷含量等制备条件将有可能控制用于组织工程的程序性凝胶侵蚀。