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dc.contributor.authorMubtasim, Noshin
dc.contributor.authorKabir, Eva Rahman
dc.contributor.authorPodder, Ashis Kumar
dc.contributor.authorBhadra, Subrata
dc.identifier.citationMubtasim, N., Kabir, E. R., Podder, A. K., & Bhadra, S. (2016). A pragmatic approach to the analysis of a combination formulation. Saudi Pharmaceutical Journal, 24(6), 689 697. doi:10.1016/j.jsps.2015.06.004
dc.descriptionThis article was published in the Saudi Pharmaceutical Journal [© 2016 Elsevier B.V.] and the definite version is available at:
dc.description.abstractThe aim of the paper was to formulate a combined oral dosage form of rosuvastatin calcium and amlodipine besylate and to develop and validate an analytical method to be adopted for both routine quality control assay and in vitro dissolution studies of the formulation. The proposed combination formulation has shown compatibility with the chosen excipients, verified through FT-IR study. A novel gradient RP-HPLC method was developed and validated according to the ICH guideline which was found to be suitable for the simultaneous estimation of rosuvastatin calcium and amlodipine besylate from the formulation. The retention time of 2.7 and 6.08 min allows the analysis of large amount of samples with less mobile phase which makes the method economic. The dissolution profiles of both the drugs in different dissolution medium were encouraging which makes the combination formulation of rosuvastatin calcium and amlodipine besylate superior and effective in achieving patient compliance.
dc.publisher© 2016 Elsevier B.V.en_US
dc.subjectRosuvastatin calcium
dc.subjectAmlodipine besylate
dc.subjectCombination formulation
dc.subjectMethod validation
dc.titleA pragmatic approach to the analysis of a combination formulationen_US
dc.contributor.departmentDepartment of Pharmacy, BRAC University

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