Research Journal of Pharmacy and Technology · 2017 · 10 citations · 0 references
PharmacyFood SciencePharmaceutical AnalysisAnalytical ChemistryChromatographic AnalysisFood AnalysisAnalytical ChromatographyBioanalytical Method ValidationChromatographic Analysis Of PharmaceuticalsChromatographyGradient ElutionLiquid ChromatographyConcentrationDrug Retention TimeHigh-performance Liquid ChromatographyHigh-performance Liquid Chromatography Method DevelopmentLiquid Chromatography-mass SpectrometryPotassium Dihydrogen PhosphateTablet Chromatographic AnalysisUltra-performance Liquid Chromatography Method Development
A new simple, rapid and sensitive Gradient Ultra Performance Liquid Chromatography (UPLC) method has been developed for the determination of Fexofenadine HCl and Montelukast Sodium. The method employs Thermo Scientific UPLC system on Waters (symmetry) (c18 1.8 micron 4.6 x 50mm) column. Best chromatographic separation was achieved by using acetonitrile: 20 mM potassium dihydrogen phosphate 80: 30 (v/v) adjusted to pH 5.5 using orthophosphoric acid as mobile phase at a flow rate of 1 ml/min and detection at 230 nm. Separation was completed within 10 min. The retention time of Fexofenadine HCl and Montelukast Sodium was found to be 1.022 and 3.281. The proposed method was found to have linearity in concentration range of 80–120 μg/ml and 96–144 μg/m. The developed method has been statistically validated and was found to be simple, precise, reproducible and accurate. The developed and validated method was successfully used for the quantitative analysis of commercially available dosage form.