Research Article
Development and Validation of Simplified RP-HPLC Method for Quantification of Candesartan Cilexetil in Commercial Formulations
Author(s): Sachin Kothawade*, Rashmi Tambare, Vishal Pande, Rucha Pardeshi, Sandesh Bole, Pranaya Misar, Balireddy Keesara, Prachi Kanawade, Kanchan Jadhav, Vijaya Padwal, Amit Lunkad and Manjusha Bhange
In order to produce antihypertensive effects, Candesartan Cilexetil (CC), a candesartan inactive prodrug, was quickly converted into active
candesartan after absorption in the Gastrointestinal (GI) tract. This research study describes the development and validation of an accurate,
precise, repeatable, easy and speedy Reverse-Phase High-Performance Liquid Chromatography (RP-HPLC) approach for measuring CC in a
formulation using reverse-phase HPLC. In this study, liquid chromatography was performed on a Zorbax SB C-18 analytical column with
dimensions of 2504.6 mm, 5 m, using a mobile phase consisting of Acetonitrile (ACN) and 0.1 percent orthophosphoric acid (pH 2.5) in a ratio of
35:65 vol/vol as the mobile phase. Results were presented as mean Standard Deviation (SD). This experiment used an injection volume of 20
microliters to measure the sample at 258 nano liters.. Read More»
DOI:
10.4172/0975-413X.16.1.197-203
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