drug release kinetics 释药动力学
iron release kinetics 释放铁动力学
drug-release kinetics 释药动力学
urea release kinetics 尿素溶出动力学
nutrient release kinetics 养分释放动力学
Chemomic release kinetics 化合物组释放动力学
aluminum release kinetics 铝释放动力学
phosphorus release kinetics 磷释放动力学
in vivo release kinetics 释药动力学
METHODS: Determining the release kinetics of tanshinone ⅡA and cryptotanshione from the film at 37.5℃ appropriate recipient by HPLC.
方法：以HPLC法测定药膜中丹参酮ⅡA和隐丹参酮在37.5℃从适宜溶出介质中的释放动力学。
参考来源 - 可生物降解丹参药膜的体外释药研究 Studies on the Release Behavior in vitro of Biodegradable Salvia miltiorrhiza Film·2,447,543篇论文数据，部分数据来源于NoteExpress
The drug release kinetics were also investigated in different releasing mediums(deionic water, 0.
目的制备盐酸氨溴索药物树脂复合物并对其体外释药动力学进行考察。
Optimal estimates of the model parameters were obtained by minimizing the difference between model simulation and experimentally measured drug release kinetics.
对模型参数的最佳评价通过最小化模型模拟和实验测定间的药物释放动力学差别来获得。
The description of dissolution profiles suggested that among the different kinetics, the first-order became the most appropriate model to describe release kinetics.
释药机制探讨表明：略有骨架，以膜控为主的控制释药模型用一级动力学方程解释较好。
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