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The present work explains the development and validation of a simple and reliable RP-HPLC method for the quantitative determination of ramipril (RMP). Chromatography was carried out by reversed-phase technique on a Fortis C18 (100 mm × 4.6 mm; 2.5 μm particle size). The optimized mobile phase was consisted of Methanol and citric acid sodium citrate buffer solution (50:50 v/v) having pH 3.0. The retention times were 3.645 min for RMP. The detection was carried out at 270 nm and a column temperature of 25 °C. The method was evaluated for the various validation parameters, such as linearity, accuracy, precision, LOD, LOQ, specificity, selectivity, and sample stability. The proposed
method was validated and successfully applied for the analysis of pharmaceutical formulations and laboratory-prepared mixture containing Ramipril respectively.
Keywords:
Ramapril, LOD, LOQ, PR-HPLC
Cite Article:
"ANALYTICAL METHOD DEVELOPMENT FOR THE DETERMINATION AND QUANTIFICATION OF RAMIPRIL IN PHARMACEUTICAL FORMULATION BY HPLC", International Journal for Research Trends and Innovation (www.ijrti.org), ISSN:2455-2631, Vol.7, Issue 9, page no.910 - 915, September-2022, Available :http://www.ijrti.org/papers/IJRTI2209124.pdf
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ISSN:
2456-3315 | IMPACT FACTOR: 8.14 Calculated By Google Scholar| ESTD YEAR: 2016
An International Scholarly Open Access Journal, Peer-Reviewed, Refereed Journal Impact Factor 8.14 Calculate by Google Scholar and Semantic Scholar | AI-Powered Research Tool, Multidisciplinary, Monthly, Multilanguage Journal Indexing in All Major Database & Metadata, Citation Generator