HPLC method development and validation of candesartan cilexetil for pharmacokinetics parameter assessment
In this study, healthy volunteers in Pakistan were asked to compare the single-dose pharmacokinetics of 16 mg of the angiotensin receptor blocker candesartan cilexetil following oral administration. Blood samples were taken over a 72-hour period while the medication was administered orally to 16 he...
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| Hlavní autor: | |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
AMMANIF
2025-06-01
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| Edice: | Journal of Contemporary Pharmacy |
| Témata: | |
| On-line přístup: | https://ammanif.com/journal/jcp/index.php/home/article/view/388 |
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