Development and optimization of a multivariate RP-UPLC method for determination of telmisartan and its related substances by applying a two-level factorial design approach: application to quality control study

Herein we report a simple, specific and rapid reverse-phase ultraperformance liquid chromatographic (RP-UPLC) method that was developed and optimized by using a two-level factorial design approach for telmisartan (TLM) and its eight critical process-related impurities. This method has excellent reso...

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Bibliographic Details
Published inAnalytical methods Vol. 6; no. 14; pp. 5168 - 5182
Main Authors Dhekale, Nitin H., Bindu, K. Hima, Kirankumar, K. Y., Gore, Anil H., Anbhule, Prashant V., Kolekar, Govind B.
Format Journal Article
LanguageEnglish
Published 01.01.2014
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Summary:Herein we report a simple, specific and rapid reverse-phase ultraperformance liquid chromatographic (RP-UPLC) method that was developed and optimized by using a two-level factorial design approach for telmisartan (TLM) and its eight critical process-related impurities. This method has excellent resolution of critical impurities, low cost of analysis and a reduced run time; moreover, it shows excellent resolution by using a BEH C18 column (100 2.1 mm, 1.7 mu m) with phosphate buffer (10 mM) as mobile phase A (pH = 2.5); acetonitrile : methanol : water as mobile phase B (75 : 15 : 10 v/v/v); column oven temperature, 30 degree C; flow rate, 0.33 mL min super(-1); and 2.0 mu L injection volume, which is monitored at 235 nm. Furthermore, the peak purity was checked for specificity, and the robustness of the method was enhanced by applying a two-level factorial design. In this design, the influence of different factors such as % methanol in mobile phase B, flow, column oven temperature, pH of the mobile phase on the responses such as resolution between impurity E and TLM, and % recovery of impurity E was investigated. Based on the response of the design, the developed method is precise, accurate, linear, successfully implemented for monitoring the reactions in R&D laboratories, and thus suitable for quality control purposes as well as the stability analysis of TLM-active pharmaceutical ingredients.
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ISSN:1759-9660
1759-9679
DOI:10.1039/c3ay42260g