Please use this identifier to cite or link to this item: http://10.9.150.37:8080/dspace//handle/atmiyauni/1671
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dc.contributor.authorShah, Pranavkumar-
dc.contributor.authorHadiyal, Sanjay-
dc.contributor.authorLalpara, Jaydeep-
dc.contributor.authorDubal, Gaurang-
dc.contributor.authorDhaduk, Bhavin-
dc.date.accessioned2024-11-19T06:12:53Z-
dc.date.available2024-11-19T06:12:53Z-
dc.date.issued2024-
dc.identifier.citationShah, P., Hadiyal, S., Lalpara, J., Dubal, G., & Dhaduk, B. (2024). Stability Indicating RP-UPLC Method for the Quantitative Determination of Degradation Impurities of Benidipine Hydrochloride & Metoprolol Succinate in Combined Dosage Form. Pharmaceutical Chemistry Journal, 57(10), 1674-1682.en_US
dc.identifier.urihttp://10.9.150.37:8080/dspace//handle/atmiyauni/1671-
dc.description.abstractA suitable RP-UPLC method for the quantitative analysis of degradation impurities of Benidipine hydrochloride & Metoprolol succinate is reported. The method was validated for specicity, linearity, range, accuracy, precision, sensitivity (LOQ and LOD), and robustness. The method shows excellent linearity with linear regression (r > 0.9950) within concentration range (0.5 to 3.0 μg/mL). LOD values were 0.14, 0.16 and, 0.15 and LOQ values were 0.42, 0.49 and 0.45 μg/mL for MET impurity-B & O and BEN impurity-2, respectively. The proposed method could be applied to routine quality control analysisen_US
dc.language.isoenen_US
dc.publisherSpringer / Pharmaceutical Chemistry Journalen_US
dc.relation.ispartofseries;57(10), 1674-1682-
dc.subjectRP-UPLC Methoden_US
dc.subjectQuantitative Determinationen_US
dc.subjectDegradation Impuritiesen_US
dc.subjectBenidipine Hydrochlorideen_US
dc.subjectMetoprolol Succinateen_US
dc.subjectCombined Dosageen_US
dc.subjectStabilityen_US
dc.titleStability Indicating RP-UPLC Method for the Quantitative Determination of Degradation Impurities of Benidipine Hydrochloride & Metoprolol Succinate in Combined Dosage Formen_US
dc.typeArticleen_US
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