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Development and validation of a high-performance thin-layer chromatographic method for the quantitative analysis of vitexin in Passiflora foetida herbal formulations
Affiliation:1. Department of Pharmacognosy, College of Pharmacy, Prince Sattam Bin Abdulaziz University, P.O. Box 173, Al-Kharj 11942, Saudi Arabia;2. Department of Pharmacognosy, Faculty of Pharmacy, King Khaled University, Abha, Saudi Arabia;3. Pharmacognosy Department, College of Pharmacy, King Saud University, Riyadh, Saudi Arabia;4. National Center for Natural Products Research, University of Mississippi, MS 38677, USA;5. Department of BioMolecular Sciences, School of Pharmacy, University of Mississippi, MS 38677, USA
Abstract:The aim of this study is the development of validated HPTLC method for the quantification of vitexin from Passiflora foetida commercial herbal formulations. The developed method was validated, in accordance with ICH guidelines for precision, accuracy, specificity and robustness. The plate was developed using ethyl acetate:methanol:water:formic acid 30:4:2:1(%, v/v/v/v) on 20 × 10 cm glass coated silica gel 60 F254 plates and the developed plate was scanned and quantified densitometrically at λ = 340 nm. Linear regression analysis revealed a good linear relationship between peak area and amount of vitexin in the range of 100–700 ng/spot. The amount of vitexin in nine commercial herbal formulations was successfully quantified by the developed HPTLC method. The developed and validated high performance thin layer chromatographic method offers a new sensitive and reliable tool for quantification of vitexinin in various herbal formulations containing Passiflora foetida.
Keywords:Vitexin  HPTLC  Validation
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