利用微通道制备超分子水凝胶载药微球及其释药性能的研究
Preparation of suparmolecular hydrogel drug-carrier microspheres by microfluidics and study on drug release properties
本文以BOC-L-苯丙氨酸为主要原料制备了一种水性凝胶因子3-{[(2S)-2-(十八酰胺基)-3-苯丙基]酰胺基}丁酸四乙基胺盐(GL-PhD),使其在微通道中发生自组装形成超分子凝胶载药微球(模型药物为盐酸环丙沙星)并研究其在不同条件下的药物释放。超分子凝胶微球的尺寸,凝胶因子浓度,环境pH和温度对超分子凝胶微球释药行为的影响结果表明,该超分子凝胶微球可以通过扩散作用将小分子药物缓慢释放到外部环境中,而且释放率高,释放时间较长,可达到控释的目的。而当凝胶因子浓度较低时,凝胶微球发生溶蚀,不能起到控制释药的作用。
In this paper,a hydrogel GL-PhD was synthesized by BOC-L-phenylalanine. The supramolecular hydrogel drug-carrier microspheres was formed by the self-assembly of the gelator in the microchannel (ciprofloxacin hydrochloride used as model drug). The drug release properties were studied in different conditions. The effects of the particle size of supramolecular hydrogel microspheres, the gelator concentration, pH and the temperature on drug release were studied. And the results showed that the drug in the supramolecular hydrogel microspheres could be released to the external environment though the diffusion effect. In addition, the release rate was high and the release time was relatively long, so the drug release could be controlled. Moreover, when the gelator concentration was too low, the gel eroded and the hydrogel microspheres could not play the role of the drug release controlling.
陈万煜、李鹏程、张丽、胡旺辉
药学生物科学研究方法、生物科学研究技术
超分子水凝胶微流控药物释放
supramolecular hydrogelmicrofluidicsdrug release
陈万煜,李鹏程,张丽,胡旺辉.利用微通道制备超分子水凝胶载药微球及其释药性能的研究[EB/OL].(2015-12-08)[2025-08-19].http://www.paper.edu.cn/releasepaper/content/201512-386.点此复制
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