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Optimized and Validated RP-HPLC Method for the Determination of Olanzapine in Pharmaceutical Formulations

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dc.contributor.author Sharifa Sultana
dc.contributor.author Islam, MD. Ashraful
dc.date.accessioned 2023-12-26T09:25:32Z
dc.date.available 2023-12-26T09:25:32Z
dc.date.issued 2014-01-01
dc.identifier.uri http://dspace.daffodilvarsity.edu.bd:8080/handle/123456789/11327
dc.description.abstract A simple, precise, accurate, rapid and reproducible RP-HPLC method has been developed for the determination of Olanzapine in pharmaceutical formulations. Chromatography was carried out on a reverse phase C-8 column (150 x 4.6 mm x 5 um length), optimum separation was achieved in 15 min using a mobile phase at a flow rate of 1 mL/min and the detection was done at 260 nm. The method produced linear responses in the concentration range from 45.2-135.6 μg/mL of Olanzapine with correlation coefficients of 1, accuracy of 99.80% and precision of 1.885%. The method was found to be reproducible for analysis of the drug in pharmaceutical formulations. The results of the analysis were tested and validated statistically for various parameters according to ICH guidelines and recovery studies confirmed the accuracy of the proposed method. en_US
dc.language.iso en_US en_US
dc.publisher Daffodil International University en_US
dc.subject Pharmaceutical technology en_US
dc.subject Pharmaceutical industry en_US
dc.title Optimized and Validated RP-HPLC Method for the Determination of Olanzapine in Pharmaceutical Formulations en_US
dc.type Article en_US


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