...体外释放 [gap=16548]s: premix membrane emulsification; microspheres; uniformity; loading efficiency; drug release in vitro ...
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drug-release in vitro 体外释放度
drug release test in vitro 体外释药试验
drug release profile in vitro 体外释药行为
drug release profiles in vitro 体外释药动力学
Drug release mechanism in vitro 体外释药机理
in vitro drug release rate 体外释药
in vitro drug release test 体外释放度测试
First, the entrapment rates (ER), drug loading (DL)and drug release in vitro are different. Second, the quality of NP is affected by thecarder material, preparation method and drug.
在这些研究中也凸显出纳米粒给药系统的一些问题和局限性，如同类性质药物的包封率、载药量、体外释放行为等存在较大差异，所采用的材料、制备方法、药物不同对所制纳米粒的质量有很大影响。
参考来源 - 载带不同性质药物的PLGA纳米粒成型质量与规律的探讨TR MPOP has good correlation between absorption in vivo and drug release in vitro.
MPOP的体外释药与体内吸收有较好的相关性。
参考来源 - 盐酸曲马多渗透泵型控释片剂的研究·2,447,543篇论文数据，部分数据来源于NoteExpress
OBJECTIVE To prepare thymopentin microspheres and investigate the drug release in vitro.
目的制备胸腺五肽微球并对其体外释放进行考察。
A few of evaluation methods for drug release in vitro of sustained-controlled matrix tablets were introduced in this review.
本文简要介绍了几种缓控释骨架片药物体外释放行为的评价方法。
According to the literature, UV spectrophotometry was developed for the investigation of physicochemical properties, content and drug release in vitro.
建立了紫外分光光度法，用于盐酸氯米帕明基本理化性质、片剂释放度和含量的测定；
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