ANALYTICAL METHOD DEVELOPMENT AND VALIDATION OF MELATONIN AND PYRIDOXINE IN TABLET DOSAGE FORM BY HPLC
Sangeeta Rathod*, Ankita Bhavsar, Bhagirath Patel
ABSTRACT
A simple, rapid and accurate High performance Liquid
Chromatography method was developed and validated for
simultaneous estimation of Melatonin and Pyridoxine in tablet dosage
form. The High performance Liquid Chromatography method has
shown adequate separation of Melatonin and Pyridoxine in its tablet
Dosage form. The separation was achieved BDS hypersil C18, with an
isocratic system of 0.2M KH2PO4 buffer (pH - 4): methanol: TEA in
the ratio of 70:30:0.1 v/v. The mobile phase at a flow rate of 1.0
ml/min, Injection volume 20μl and wavelength of detection used was
244 nm. The retention time for Melatonin and Pyridoxine were
obtained as 3.760 min and 6.107 min, respectively. The linearity of the proposed method was
investigated in the range of 3-9 μg/ml and 10-30μg/ml for Melatonin and Pyridoxine
respectively. Correlation coefficient was 0.9939 and 0.9995 for Melatonin and Pyridoxine
respectively. The developed method was validated as per International conference
Harmonization (ICH) guideline for its accuracy, precision, Limit of detection and Limit of
quantitation.
Keywords: Melatonin, Pyridoxine, HPLC method development, Validation.
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