• Individual solutions may be directly prepared in the dissolution medium.

    直接用溶出介质制备每一个溶液。

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  • The dissolution step is the release of the drug inthe dissolution medium and sampling. The analytical finish is defined insection 3.

    溶出步骤是指药物在溶出介质中的释放和取样,分析方法的定义详见第3章节分析方法。

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  • Insome cases, where the drug substance can degrade in the dissolution medium(e. g. , dosage forms containing aspirin), it is useful to carry out themeasurements at the isosbestic point.

    在某些情况下,药物在溶出介质中降解(例如,含有阿司匹林的制剂),适合在在等吸收点完成测定。

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  • Famotidine dispersible tablets were prepared. The influence of PVP concentration, sodium starch glycolate quantity and different medium on disintegration and dissolution rate is discussed.

    探讨了聚乙烯吡咯烷酮浓度,羧甲基淀粉钠用量对法莫替丁分散片崩解的影响及不同介质对其溶出的影响。

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  • The present invention relates to a pharmaceutical composition with improved dissolution of lipophilic drugs in an aqueous medium.

    本发明涉及一种亲脂性药物在水介质中溶出得以改善的药物组合物。

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  • CONCLUSIONS: the dissolution of TCRC in above medium were different only in a several time points, but there was no difference in the total cumulative dissolution.

    结论:TCRC在不同介质中的累积释放度只在几个时间点有差异,而总的释放度无差异。

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  • CONCLUSIONS: the dissolution of TCRC in above medium were different only in a several time points, but there was no difference in the total cumulative dissolution.

    结论:TCRC在不同介质中的累积释放度只在几个时间点有差异,而总的释放度无差异。

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