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可降解微球/凝胶复合给药系统释药动力学

haracterizing the drug release from the biodegradable microsphere incorporated hydrogel drug delivery system

中文摘要英文摘要

将可生物降解微球和可注射凝胶结合的埋植给药系统,可实现长期稳定给药。本论文以含有纳曲酮的聚乳酸-乙醇酸共聚物(PLGA)微球和甲基纤维素温敏凝胶构成的释药系统为例,研究了药物在微球/凝胶复合系统中的释放动力学特征和模型。在微球/凝胶复合系统中,药物的释放主要受其在微球中的释放控制,可用微球释药模型模拟;水凝胶改变微球存在环境和分子扩散阻力,从而使药物扩散系数减小,微球的溶蚀速率降低,达到最大溶蚀速率的时间延长,从而使释药速率降低并更加平稳,将上述影响引入微球释药模型建立的微球-凝胶系统释药模型,模拟结果和实验数据一致。通过调整微球材料的分子量和亲疏水性,可实现药物超过60天的恒速释放。

Biodegradable microspheres incorporated injectable gelling drug delivery system has great potential in implanted drug delivery for long-term controlled drug release. In the present study, drug release in vitro was investigated into a model system which was composed by naltrexone-loaded PLGA microspheres and thermosensitive hydrogel consisted of methylcellulose, polyethylene glycol, sodium citrate and sodium alginate. In the microspheres /hydrogel composite system, drug release was dominated by drug diffusion in the microspheres and could be described with the model established on drug release from biodegradable polymeric microspheres. The hydrogel impacted on the porosity, erosion and degradation of the microspheres, which resulted in the smaller drug diffusion coefficient, lower erosion rate and prolonged period to reach the maximal erosion rate and, therefore, reduced and stabilized the drug release rate. Those impacts of hydrogel were presented in the drug release model based on drug release from biodegradable polymeric microspheres and the developed model was well consistent with the experiment.

孙佳丽、丁富新、林莹、蒋国强

医药卫生理论药学医学研究方法

药剂学埋植给药凝胶微球释药动力学

drug deliveryimplanthydrogelmicrospheredrug release

孙佳丽,丁富新,林莹,蒋国强.可降解微球/凝胶复合给药系统释药动力学[EB/OL].(2010-12-31)[2025-08-10].http://www.paper.edu.cn/releasepaper/content/201012-1410.点此复制

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