Analytical method development and validation for simultaneous estimation of Fimasartan Potassium Trihydrate and Cilnidipine in synthetic mixture by HPLC for the …

RG Sojitra, UJ Chotaliya - Future Journal of Pharmaceutical Sciences, 2021 - Springer
Background A specific, accurate, precise, robust, and cost-effective HPLC method was
developed and validated for quantitative analysis of Fimasartan Potassium Trihydrate and …

[PDF][PDF] Stability indicating method development and validation of fimasartan by reverse phase high performance liquid chromatography in bulk and pharmaceutical …

A Sruthi, P Uttam Prasad - Asian J Pharm Clin Res, 2021 - pdfs.semanticscholar.org
Objective: A rapid, sensitive and specific reverse phase High performance liquid
Chromatography (RP-HPLC) method was developed for the estimation of Fimasartan in bulk …

[PDF][PDF] Development and validation of novel rp-hplc method for related substances in chlorthalidone and fimasartan formulations

K Rai, N Rao - hypertension, 2020 - wjpr.s3.ap-south-1.amazonaws.com
The objective of the present work was to develop and validate a novel stability-indicating
method for the simultaneous estimation of chlorthalidone and fimasartan potassium …

[PDF][PDF] Analytical method development and validation of Ramipril and Candesartan Cillexetil in synthetic mixture

A Nagar, S Deore, A Bendale, R Kakade… - Innov Pharm …, 2020 - academia.edu
Aim: The aim of the study was to develop a rapid, accurate, and precise ratio spectra
derivative spectroscopic high-performance liquid chromatography method and validated for …

Simultaneous estimation of amlodipine besylate, Rosuvastatin calcium and Fimasartan potassium trihydrate combination used in the treatment of hypertension using …

DA Kansara, UK Chhalotiya, HM Kachhiya, IM Patel… - SN Applied …, 2020 - Springer
The proposed sensitive, precise, and accurate reverse phase-liquid chromatography (RP-
LC) method is used for simultaneous estimation Amlodipine besylate, Rosuvastatin calcium …

[PDF][PDF] Development and validation of stability indicating gradient RP-HPLC method for simultaneous estimation of telmisartan and chlorthalidone in bulk API and fixed …

BR Chaudhary, JB Dave - World J Pharm Res, 2017 - academia.edu
Telmisartan and Chlorthalidone is an approved widely used antihypertensive fixed dose
combination of angiotensin receptor blocker and diuretic drugs. The main objective was to …

Validated LC–MS/MS Assay for the quantitative determination of Fimasartan in human plasma: application to pharmacokinetic studies

SH Yoon, S Oh, HS Kim, SJ Yi, KS Yu… - Journal of …, 2015 - academic.oup.com
A simple, rapid and sensitive liquid chromatography–tandem mass spectrometry (LC–
MS/MS) method for the quantification of a newly developed antihypertensive agent …

Fully validated ultra-performance liquid chromatography-tandem mass spectrometry method for the determination of Fimasartan in human plasma

JY Hyun, HJ Kim, MR Gwon, HW Lee, SJ Seong… - Analytical …, 2015 - Springer
Fimasartan is a novel angiotensin II receptor blocker with strong anti-hypertensive activity. In
this study, a more rapid and sensitive ultra-performance liquid chromatography–tandem …

[PDF][PDF] Simultaneous estimation of azilsartan and cilnidipine in bulk by RP-HPLC and assessment of its applicability in marketed tablet dosage form

SM ANDHALE, APG NIKALJE - hypertension, 2022 - academia.edu
Objective: This study aims to build up the RP-HPLC process for Azilsartan and Cilnidipine
and authenticate the RP-HPLC process according to ICH validation code Q2R1. Methods …

RP-HPLC method development and validation for simultaneous estimation of efonidipine hydrochloride ethanolate and telmisartan in their synthetic mixture

SD Adeshra, DB Meshram - International Journal of Pharmaceutics and …, 2021 - neliti.com
A Novel, selective, accurate and rapid Reversed Phase High Performance Liquid
Chromatographic (RPHPLC) method for the analysis of Efonidipine Hydrochloride …