Development and validation of a reversed-phase ion-pair liquid chromatography method for the determination of magnesium ascorbyl phosphate and ... [An article from: Analytica Chimica Acta]
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PublisherElsevier
ISBN / ASINB000PDT8OQ
ISBN-13978B000PDT8O4
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Description
This digital document is a journal article from Analytica Chimica Acta, published by Elsevier in 2006. The article is delivered in HTML format and is available in your Amazon.com Media Library immediately after purchase. You can view it with any web browser.
Description:
A reversed-phase ion-pair high-performance liquid chromatographic method was developed and validated for the determination of magnesium ascorbyl phosphate and melatonin in cosmetic creams. The determination was performed on a BDS C 18 analytical column (250x4.6mm i.d., 5@mm particle size); the mobile phase consisted of 0.020M tetrabutylammonium hydroxide and 0.025M potassium dihydrogen phosphate (pH 6.8) mixed with acetonitrile in a ratio (77:23, v/v) and pumped at a flow rate 1.00mlmin^-^1. The UV detector was operated at 260nm. The retention times of the magnesium ascorbyl phosphate, melatonin and chlorthalidone that was used as internal standard, were 6.55, 9.18 and 11.07min, respectively. Calibration graphs are linear (r better than 0.9990, n=6), in concentration range 1.00-10.00@mgml^-^1 for magnesium ascorbyl phosphate and 0.63-6.25@mgml^-^1 for melatonin. The intra- and inter-day R.S.D. values were less than 6.0%, while the relative percentage error E"r was less than 3.5% (n=5). The quantitation limits were 0.69 and 0.47@mgml^-^1, for magnesium ascorbyl phosphate and melatonin, respectively. The method was applied to the analysis of a cosmetic cream and proved to be suitable for rapid and reliable quality control.
Description:
A reversed-phase ion-pair high-performance liquid chromatographic method was developed and validated for the determination of magnesium ascorbyl phosphate and melatonin in cosmetic creams. The determination was performed on a BDS C 18 analytical column (250x4.6mm i.d., 5@mm particle size); the mobile phase consisted of 0.020M tetrabutylammonium hydroxide and 0.025M potassium dihydrogen phosphate (pH 6.8) mixed with acetonitrile in a ratio (77:23, v/v) and pumped at a flow rate 1.00mlmin^-^1. The UV detector was operated at 260nm. The retention times of the magnesium ascorbyl phosphate, melatonin and chlorthalidone that was used as internal standard, were 6.55, 9.18 and 11.07min, respectively. Calibration graphs are linear (r better than 0.9990, n=6), in concentration range 1.00-10.00@mgml^-^1 for magnesium ascorbyl phosphate and 0.63-6.25@mgml^-^1 for melatonin. The intra- and inter-day R.S.D. values were less than 6.0%, while the relative percentage error E"r was less than 3.5% (n=5). The quantitation limits were 0.69 and 0.47@mgml^-^1, for magnesium ascorbyl phosphate and melatonin, respectively. The method was applied to the analysis of a cosmetic cream and proved to be suitable for rapid and reliable quality control.
