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Stability Indicating RP-UPLC Method for the Quantitative Determination of Degradation Impurities of Benidipine Hydrochloride & Metoprolol Succinate in Combined Dosage Form

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dc.contributor.author Shah, Pranavkumar
dc.contributor.author Hadiyal, Sanjay
dc.contributor.author Lalpara, Jaydeep
dc.contributor.author Dubal, Gaurang
dc.contributor.author Dhaduk, Bhavin
dc.date.accessioned 2024-11-19T06:12:53Z
dc.date.available 2024-11-19T06:12:53Z
dc.date.issued 2024
dc.identifier.citation Shah, 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.uri http://10.9.150.37:8080/dspace//handle/atmiyauni/1671
dc.description.abstract A 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 analysis en_US
dc.language.iso en en_US
dc.publisher Springer / Pharmaceutical Chemistry Journal en_US
dc.relation.ispartofseries ;57(10), 1674-1682
dc.subject RP-UPLC Method en_US
dc.subject Quantitative Determination en_US
dc.subject Degradation Impurities en_US
dc.subject Benidipine Hydrochloride en_US
dc.subject Metoprolol Succinate en_US
dc.subject Combined Dosage en_US
dc.subject Stability en_US
dc.title Stability Indicating RP-UPLC Method for the Quantitative Determination of Degradation Impurities of Benidipine Hydrochloride & Metoprolol Succinate in Combined Dosage Form en_US
dc.type Article en_US


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