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
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
In the drug release kinetics investigation, influences of the content of drug, the microsphere size and the content of crossing-linker on the drug-release were studied.
在体外溶出实验中对阿霉素磁性毫微粒体外释放性能的影响主要考察了三个因素：毫微粒平均粒径大小、毫微粒的载药量以及交联剂含量。
OBJECTIVE To prepare the Panax Notoginseng Saponines (PNS) bioadhesive tablets, and to study their release kinetics and bioadhesive tablets force to rabbit small intestine in vitro.
目的研制三七总皂苷生物黏附片，考察其体外释药动力学、对离体肠黏膜的黏附力。
CONCLUSION the theoretical values obtained by non-linear least square model fit program is near to the test values. The theoretical equations can describe accurately the release kinetics of pellets.
结论采用非线性最小二乘法拟合释药动力学方程得到的理论值更接近真实值，说明由非线性最小二乘法模型嵌合通用程序得到的动力学方程能准确表征微丸的释药动力学。
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