...;;崩解时间 [gap=678]integrating tablets;microcrystaline cellulose;cross-linked polyvinylpyrrolidone;disintegration time ...
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Microemulsified performance,disintegration time,content uniformity,and release profiles in vitro were investigated. The surface feature of TGF SMEOFDF was detected by scanning electron microscope and the crystal form of drug was characterized by differential scanning calorimetry.
考察其自微乳化性能、崩解时间、体外释放度等体外性质,采用差示扫描量热法和扫描电子显微镜表征药物晶型和膜的表面形态。
参考来源 - 银杏叶总黄酮自微乳化口腔速溶膜的制备及其性质研究·2,447,543篇论文数据，部分数据来源于NoteExpress
结论：所选处方合理，崩解时间短，分散均匀性好。
Conclusion: The dispersible tablet dissolved faster and dispersed uniformly.
将吸水特性常数与片剂崩解时间进行比较，考察水渗透与片剂崩解的关系。
The characteristic constant of water uptake was compared with disintegration time in order to investigate the relationship between water uptake and disintegration.
方法采用正交实验重点考察不同含量泡腾剂对于空白片剂口腔内及体外崩解时间的影响；
Methods Effervescent was evaluated carefully including its influence on the disintegrating time of blank tablets in vitro and in vivo.
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