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Development of a dissolution method for lumefantrine and artemether in immediate release fixed dose artemether/lumefantrine tablets
BACKGROUND: Dissolution of artemether (ART) and lumefantrine (LUM) active pharmaceutical ingredients (APIs) in fixed dose combination (FDC) ART/LUM tablets is one of the critical quality attributes. Thus, the verification of the release profile of ART and LUM from FDC ART/LUM tablets using a robust...
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| 出版年: | Malar J |
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| 主要な著者: | , , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
BioMed Central
2020
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| 主題: | |
| オンライン・アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7140584/ https://ncbi.nlm.nih.gov/pubmed/32264882 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12936-020-03209-5 |
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