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溶出度

网络dissolution; dissolution rate; dissolution test

溶出度

网络释义

溶出度

dissolution

制药行业专业英语词典 - 豆丁网 ... dissolubility 溶解度 dissolution 溶出度 disintegration 崩解时限 ...

dissolution rate

　　药物溶出度(dissolution rate)是指药物从片剂、胶囊剂或颗粒剂等固体制剂在规定的介质中溶出的速率和程度。由于药物的溶出 …

dissolution test

1.3.3.7溶出度(dissolution test)[6]药物的溶出度是微丸质量控制的关键，本研究主要以 10 min药物的累积释放百分率（P10）为 …

dissolubility

...中医药大学中药学院中药制药系 72 1. 定义： 溶出度（dissolubility）：在规定介质中药物从片剂或胶囊剂等固体制剂溶出的 …

dissulution

医药词汇-医药翻译词汇 ... 含量均匀度 content uniformity 溶出度 dissulution 离子对高效液相色谱法 ion-pair，HPLC ...

hollow suppositories

hollow glass microspheres_翻译 ... 空芯纱： Hollow yarn 溶出度： hollow suppositories 空心球： Hollow sphere ...

Y Rt

④ 平均式中 Y nt 可为试验药品的平均溶出度 ( Y Tt ) 或对照药品的平均溶出度 ( Y Rt ) 。 ③ 计算试验药品与对照药品的平均 …

Y Tt

④ 平均式中 Y nt 可为试验药品的平均溶出度 ( Y Tt ) 或对照药品的平均溶出度 ( Y Rt ) 。 ③ 计算试验药品与对照药品的平均 …

例句：

Results : The release rate of nicardipine hydrochloride decreased considerably with the growth of the thickness of membrane and Mw of PLA .

结果：盐酸尼卡地平体外溶出度随着膜厚度及聚乳酸分子量增大而显著减小。

The BCA method and in vitro adhesive analogue were adopted to determine release behavior of the adhesive pellets and their adhesiveness .

采用离体黏附模型及二喹啉甲酸（BCA ）法测定黏附微丸的黏附性及溶出度。

Objective : To improve the dissolution rate of a poorlywatersoluble drug, tanshinone .

目的：提高难溶性药物丹参酮的体外溶出度。

Methods With the dissolution rate as index , the orthogonal design L9(34) was used to screen out the best preparation technology .

方法以溶出度为指标进行考察，用正交设计优化多司马酯胶囊的生产工艺。

Conclusion : Dissolutions of tablets(capsules) produced by different factories could be greatly different .

结论：不同厂家生产的同类产品溶出度有明显不一致性。

Method : The dissolution of Amoxicillin capsules determined by the different dilution steps of self reference were compared .

方法：自身对照采用不同稀释步骤测定溶出度进行比较。

Dissolution of itraconazole self-emulsifying capsule was investigated, taking the commercial capsule as reference .

以市售硬胶囊为参比制剂测定伊曲康唑自乳化胶囊的溶出度。

The results show that the application of grey model to simulation of the release data of drug is satisfactory .

结果表明，用灰色模型拟合药物溶出度数据具有令人满意的效果。

Coating formula of Nimesulide sustained release pellet capsules and the dissolution in vitro were tested using orthogonal design methods.

制备尼美舒利缓释微丸胶囊及测定体外溶出度。

Objective To obtain the optimal prescription of Mosapride Citrate Tablets(MCT) to improve the tablets dissolution .

目的筛选枸橼酸莫沙必利片的最佳工艺处方，提高溶出度。

Objective : To establish a method for determination of dissolution of Reserpine in compound capsules of anti hypertension.

目的：建立复方降压胶囊中利血平的溶出度测定方法。

Objective To observe the influence of menstruums degassing degree on the experiment results in the apparatus suitability test .

目的探索溶出度仪的系统适用性校正方法中溶剂的脱气程度对实验结果的影响。

Conclusion : The dissolution of indapamide capsules are coincidence with requirement .

结论：所研制的吲达帕胺胶囊溶出度符合要求。

Results: The results showed that solid dispersion give much higher improvement than physical mixture in the dissolution rate.

结果体外实验结果表明，固体分散体对尼莫地平溶出度的提高大大优于物理混合物。

Subjective: To enhance the dissolution rate of ursolic acid from its preparation .

目的：提高制剂中乌索酸的溶出度。

Objective To optimize the preparation procedure of sultamicillin tosilate capsules and to improve the dissolution .

目的优化托西酸舒他西林胶囊制备工艺，使其溶出度提高。

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