Analytical method development and validation of Amlodipine besylate in tablet dosage form
نویسندگان
چکیده
منابع مشابه
Development and Validation of Rp-hplc Method for Simultaneous Estimation of Lisinopril and Amlodipine Besylate in Tablet Dosage Form
A simple, specific, precise, and accurate reversed-phase HPLC method was developed and validated for simultaneous estimation of lisinopril and amlodipine besylate in tablet dosage forms. The separation was achieved by Hypersil ODS-BP C18 column (250 mm × 4.6 mm; 5.0 μm) using methanol: phosphate buffer at pH 6 adjusted with orthophosphoric acid (30: 70, v/v) as eluent, at a flow rate of 1 mL/mi...
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متن کاملSpectrophotometric Estimation of Amlodipine Besylate in Bulk and in Tablet Dosage Form
A simple UV spectrophotometric method for the analysis of Amlodipine Besylate was developed to analyze the drug in bulk and in tablet formulation. In this method the simple UV spectrum of Amlodipine Besylate in aqueous ethanol (30% v/v) was obtained which exhibits absorption maxima (λ max) at 239.40 nm. The Beers law ranges was followed in the concentration range of 5-60 μg/ml. The proposed met...
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Article history: Received on: 08/09/2012 Revised on: 19/09/2012 Accepted on: 24/09/2012 Available online: 28/09/2012 A simple, precise and rapid reverse-phase HPLC method has been developed and subsequently validated for the simultaneous estimation of Amlodipine besylate and Enalapril maleate from their combination drug product. The proposed RP-HPLC method utilizes a Phenomenex C18, 5 μm, 250 m...
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ژورنال
عنوان ژورنال: Journal of Drug Delivery and Therapeutics
سال: 2019
ISSN: 2250-1177
DOI: 10.22270/jddt.v9i4-a.3459