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A Validated RP-HPLC Method for the Estimation of Quetiapine in Bulk and Pharmaceutical Formulations
Author(s) -
D. Suneetha,
A. Lakshmana Rao
Publication year - 2010
Publication title -
journal of chemistry
Language(s) - English
Resource type - Journals
eISSN - 2090-9063
pISSN - 2090-9071
DOI - 10.1155/2010/105963
Subject(s) - quetiapine , detection limit , chromatography , quetiapine fumarate , phosphate buffered saline , dosage form , acetonitrile , particle size , pharmaceutical formulation , chemistry , phase (matter) , high performance liquid chromatography , materials science , analytical chemistry (journal) , computer science , atypical antipsychotic , schizophrenia (object oriented programming) , organic chemistry , antipsychotic , programming language
A new, simple, specific, sensitive, rapid, accurate and precise RP-HPLC method was developed for the estimation of quetiapine in bulk and pharmaceutical formulations. Quetiapine was chromatographed on a reverse phase C18 Waters column (75x4.6 mm I.D., particle size 3.5 μm) in a mobile phase consisting of phosphate buffer (pH 3.0 adjusted with orthophosphoric acid) and acetonitrile in the ratio 40:60 v/v. The mobile phase was pumped at a flow rate of 0.8 mL/min with detection at 291 nm. The detector response was linear in the concentration of 20-120 μg/mL. The limit of detection and limit of quantitation was found to be 0.2 and 0.75 μg/mL, respectively. The intra and inter day variation was found to be less than 1%. The mean recovery of the drug from the solution was 99%. The proposed method is simple, fast, accurate, precise and reproducible hence, it can be applied for routine quality control analysis of quetiapine in bulk and pharmaceutical formulations

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