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。
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。
Understanding the kinetics of these reactions would be helpful to activate only the relevant pathways that would generate the desired flavors with out the release of undesirable flavors.
了解这些反应动力学的研究将有助于相关方法的激活而产生想要的口味和除去不良风味。
Microbial amount plays a key role in kinetics of pollutants release from sediments. The new method can measure microorganism amount rapidly.
微生物数量在底泥污染物释放动力学中起着关键性作用，新型方法可以快速检测微生物总量。
Conclusion This high performance liquid chromatography method is simple, sensitive and accurate. It is suitable for released kinetics study of controlled-release microspheres of BCNU loading in vitro.
结论本法准确可靠，操作简便，适用于缓释bcnu微球的体外药物释放动力学研究。
The results indicated that the sustained-release tablets had an expected sustained-release quality, and drug release pattern was in accorded with the first order kinetics.
结果表明，制得的酒石酸美托洛尔缓释片具有明显的缓释作用，体外释放符合一级释药动力学规律。
The release and re-adsorption kinetics of Cd in seawater of different salinity of dredged sediments from Yuandang Lake has been studied in simulation.
在相同条件下释放量（释放率）随介质盐度升高而增大，而被吸附能力降低。
The results indicated that the sustained release tablets had an expected sustained release quality, and the drug release pattern was in accorded with the first order kinetics.
结果表明：研制缓释片的缓释效果良好，药物的释放符合一级动力学规律。
The results indicated that the sustained release tablets had an expected sustained release quality, and the drug release pattern was in accorded with the first order kinetics.
结果表明：研制缓释片的缓释效果良好，药物的释放符合一级动力学规律。
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