药物输送
PLGA公司
相位反转
化学
化学工程
反演(地质)
色谱法
动力学
相(物质)
材料科学
活性成分
反应速率常数
动力学(音乐)
纳米技术
药品
剂型
毒品携带者
增长率
化学物理
控制释放
分析化学(期刊)
缓冲溶液
作者
Paul Graham,K.J. Brodbeck,A. J. McHugh
标识
DOI:10.1016/s0168-3659(98)00158-8
摘要
Dark ground optical microscopy, electron microscopy, and high performance liquid chromatography (HPLC) have been used to quantify the effects of formulation changes on the phase inversion dynamics and in vitro drug release properties of a PLGA-based drug delivery system. Gel growth rates and water influx rates are determined from plots of the square of the respective front motion with time. Results show that additives that accelerate the solution gelation rate at constant morphology result in high initial release rates. Conversely, additives that slow the rate of gelation dramatically reduce the initial drug release rate and lead to a more dense sponge-like morphology. Moreover, the phase inversion dynamics and morphology are the same regardless of whether the solutions are quenched with water, a PBS buffer solution or horse serum.
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