Please use this identifier to cite or link to this item: http://10.9.150.37:8080/dspace//handle/atmiyauni/1671
Title: Stability Indicating RP-UPLC Method for the Quantitative Determination of Degradation Impurities of Benidipine Hydrochloride & Metoprolol Succinate in Combined Dosage Form
Authors: Shah, Pranavkumar
Hadiyal, Sanjay
Lalpara, Jaydeep
Dubal, Gaurang
Dhaduk, Bhavin
Keywords: RP-UPLC Method
Quantitative Determination
Degradation Impurities
Benidipine Hydrochloride
Metoprolol Succinate
Combined Dosage
Stability
Issue Date: 2024
Publisher: Springer / Pharmaceutical Chemistry Journal
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.
Series/Report no.: ;57(10), 1674-1682
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
URI: http://10.9.150.37:8080/dspace//handle/atmiyauni/1671
Appears in Collections:01. Journal Articles

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