Pharmaceutica Analytica Acta · 2010 · 16 citations · 6 references
PharmacyChemistryPharmaceutical AnalysisAnalytical ChemistryChromatographic AnalysisMass Spectrometric AnalysisAnalytical ChromatographyChromatographic Analysis Of PharmaceuticalsChromatographyLiquid ChromatographyStationary Phase ChemistryHigh-performance Liquid ChromatographyHigh-performance Liquid Chromatography Method DevelopmentQuality Control AnalysisRetention Time AnalysisSolution Stability
A simple, fast and precise reversed phase high performance liquid chromatographic method has been developed for the simultaneous determination of Camylofin dihydrochloride and Diclofenac Potassium using Methylparaben as an internal standard. Efficient__chromatographic separation was achieved on Inertsil C 18 column (250mm x 4.6 mm, 5m) as stationary phase with a mobile phase comprising of 0.05 M KH 2 PO 4 in water : Methanol (35:65,v/v) at a flow rate of 1.5mL min -1 , column temperature of 27C and UV detection at 220 nm. The retention time of Methylparaben, Camylofin dihydrochloride and Diclofenac potassium were 3.60 min, 4.85 min and 13.10 min respectively. The proposed method was validated for linearity, accuracy, precision, sensitivity, robustness and solution stability. Linearity, accuracy and precision were found to be acceptable over the ranges of 250-750g mL -1 for both camylofin dihydrochloride and diclofenac potassium. The test solution was found to be stable for 48 h. It can be conveniently adopted for routine quality control analysis.
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Practical HPLC Method Development
Analytical Chemistry · 1993 · 1.4K citations
Business, Pharmaceutical Analysis, Norm-referenced Assessment +5
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Business, Pharmaceutical Analysis, Norm-referenced Assessment +5
“Practical HPLC method development”, 2nd edition
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Bioavailability of diclofenac potassium at low doses
Burkhard Hinz, Julia Chevts, Bertold Renner et al. · British Journal of Clinical Pharmacology · 2004 · 72 citations · Full text