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Title: HPLC method development and validation of candesartan cilexetil for pharmacokinetics parameter assessment
Authors: Israr Fatima
Journal: Journal of Contemporary Pharmacy
| Category | From | To |
|---|---|---|
| Y | 2023-07-01 | 2024-09-30 |
Publisher: AMMANIF PUBLISHER (PRIVATE) LIMITED
Country: Pakistan
Year: 2025
Volume: 9
Issue: 1
Language: en
Keywords: BioequivalenceRP-HPLCcandesartanSingle-Dose Pharmacokinetics
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 healthy individuals. Following a freeze-thaw cycle, the samples were subjected to reversed-phase HPLC analysis at a wavelength of 258 nm using an isocratic mobile phase consisting of potassium dihydrogen phosphate and methanol (25:75 v/v). Pharmacokinetic parameters such as Cmax, Tmax, t1/2, Ka, Vd, and AUC were computed.
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