drug release in vitro 体外释放 ; 体外药物释放
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
CONCLUSION The TFH tablet has sustained release property in vitro. The drug release pattern is in accord with Weibull distribution.
结论醋柳黄酮缓释片缓释效果显著，体外释放符合威布尔分布模型。
Vitamin B12 was selected as a model drug and the in vitro release properties was studied.
以维生素b12为模型药物，研究药物的释放性质。
OBJECTIVE To evaluate drug release properties in vitro of the hydrogel films made of cross-linked hyaluronic acid derivatives.
目的对交联透明质酸衍生物制备的载药水凝胶膜进行体外药物释放研究。
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