RP HPLC METHOD DEVELOPMENT AND ITS VALIDATION FOR SIMULTANEOUS DETERMINATION OF TELMISARTAN AND FINOFIBRATE
P. Pooja*, Dr. P. Arun, P. Shailendra, D. Neelesh Kumar and P. Bhavesh
Abstract
A reversed phase liquid chromatographic method with UV detection
290 nm for Telmisartan and Finofibrate assay in human plasma was
developed and validated. chromatographic separations was achieved on
Phenomenex(c-18 250 mm x 4.60 mm) column kept at 4-35tem with
mobile phase (methenoal:water) at a flow rate of 1ml /mint the method
was validated for its specificity, linearity, accuracy, LOD, LOQ and
robustness based on ICH guidelines. The validation studies revealed
satisfactory reasarch proposed method has been applied for the
quantification of telmisartan and Finofibratein commercial samples.
Keywords: RP-HPLC, Telmisartan and Finofibrate, retention time, validations-linearity, accuracy, precision.
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