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HPTLC method for estimation of Olmesartan medoxomil in tablet formulation with stability studies

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dc.contributor.author Verma, Prabhakar Kumar
dc.contributor.author Kamboj, Vipan Kumar
dc.date.accessioned 2023-01-20T04:34:24Z
dc.date.available 2023-01-20T04:34:24Z
dc.date.issued 2013-01-20
dc.identifier.citation Verma, P. K., & Kamboj, V. K. (2013). HPTLC method for estimation of olmesartan medoxomil in tablet formulation with stability studies. Pakistan Journal of Pharmaceutical Sciences, 26(1), 209-216. en_US
dc.identifier.issn 1011-601X
dc.identifier.uri http://142.54.178.187:9060/xmlui/handle/123456789/16127
dc.description.abstract A rapid resolution high performance thin layer chromatography (HPTLC) method has been developed and validated for estimation of Olmesartan medoxomil in tablet formulations. This paper describes accurate, precise, specific and reproducible method and its degradation products, related impurities for assessment of purity of bulk drug and stability of its tablet formulations. The method involve silica gel 60 F254 high performance thin layer chromatography and densitometric detection at 264 nm using toluene - acetonitrile- methanol - ethyl acetate - acetic acid (5:3.5:0.3:1:0.3 v/v/v/v). Calibration curve ranges between 300-800 ng/spot-1 Olmesartan medoxomil. Experimental design was involved forced degradation of drug, optimization of mobile phase, detection made and other chromatographic phase and study of linearity range. The total time for chromatographic separation was 6 min with a total analysis time 15 min. The proposed method was validated for its linearity, precision, recovery studies and robustness. en_US
dc.language.iso en en_US
dc.publisher Karachi: Pakistan Botanical Society, University of Karachi en_US
dc.subject Olmesartan medoxomil en_US
dc.subject HPTLC en_US
dc.subject validation, experimental design. en_US
dc.title HPTLC method for estimation of Olmesartan medoxomil in tablet formulation with stability studies en_US
dc.type Article en_US


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