Journal of Pharmaceutics · 2013 · 16 citations · 17 references
PharmacyChemistryPharmaceutical AnalysisAnalytical ChemistryAnalytical ToxicologyChromatographic AnalysisAnalytical ChromatographyChromatographic Analysis Of PharmaceuticalsChromatographic Method ValidationChromatographyLiquid ChromatographyAnalytical Liquid ChromatographyChromatographic InstrumentationChromatographic QuantificationHigh-performance Liquid ChromatographyHigh-performance Liquid Chromatography Method DevelopmentInternal Standard AnalysisLinearityLinearity Assessment
A sensitive and precise RP-HPLC method has been developed for the simultaneous estimation of clidinium bromide (CDB) and chlordiazepoxide (CDZ) in pure and pharmaceutical formulations. The separation was achieved on a Nucleodur C8 (250 × 4.6 mm i.d., 5 μm particle size) column at 25°C. CH3CN-MeOH-NH4OAc 0.1M (30 : 40 : 30, v/v/v) was used as the mobile phase at a flow rate of 1.0 mL min(-1) and detector wavelength at 218 nm. Almotriptan (ALT) was used as internal standard. The validation of the proposed method was carried out for linearity, accuracy, precision, LOD, LOQ, and robustness. The method showed good linearity in the ranges of 2.5-300.0 and 3.0-500.0 μg mL(-1) for CDB and CDZ, respectively. The percentage recovery obtained for CDB and CDZ was 100.40-103.38 and 99.98-105.59%, respectively. LOD and LOQ were 0.088 and 0.294 μg mL(-1) for CDB and 0.121 and 0.403 μg mL(-1) for CDZ, respectively. The proposed method was successfully applied to the determination of CDB and CDZ in combined dosage forms and the results tallied well with the label claim.
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Limit of detection. A closer look at the IUPAC definition
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