Department of Pharmaceutical Technology, University of Regensburg, Germany.
Biomacromolecules. 2010 Feb 8;11(2):496-504. doi: 10.1021/bm901235g.
Tethering drug substances to a gel network is an effective way of controlling the release kinetics of hydrogel-based drug delivery systems. Here, we report on in situ forming, biodegradable hydrogels that allow for the covalent attachment of peptides or proteins. Hydrogels were prepared by step-growth polymerization of branched poly(ethylene glycol). The gel strength ranged from 1075 to 2435 Pa; the degradation time varied between 24 and 120 h. Fluorescence recovery after photobleaching showed that fluorescently labeled bovine serum albumin (FITC-BSA) was successfully bound to the gel network during gel formation. Within 168 h, the mobility of the tethered molecules gradually increased due to polymer degradation. Using FITC-BSA and lysozyme as model proteins, we showed the potential of the developed hydrogels for time-controlled release. The obtained release profiles had a sigmoidal shape and matched the degradation profile very well; protein release was complete after 96 h.
将药物物质连接到凝胶网络是控制水凝胶药物输送系统释放动力学的有效方法。在这里,我们报告了原位形成的、可生物降解的水凝胶,这些水凝胶允许共价连接肽或蛋白质。水凝胶通过支化聚乙二醇的逐步聚合制备。凝胶强度范围为 1075 至 2435 Pa;降解时间在 24 至 120 小时之间变化。光漂白荧光恢复表明,荧光标记的牛血清白蛋白(FITC-BSA)在凝胶形成过程中成功结合到凝胶网络中。在 168 小时内,由于聚合物降解,连接分子的迁移率逐渐增加。使用 FITC-BSA 和溶菌酶作为模型蛋白,我们展示了开发的水凝胶用于时间控制释放的潜力。获得的释放曲线呈 S 形,与降解曲线非常吻合;96 小时后蛋白质完全释放。