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American Journal of Pharmacy and Health Research

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Development and Validation of Common RP-HPLC Method for Estimation of Selected Triptans

Published in June 2015 Issue 6 (Vol. 3, Issue 6, 2015)

Development and Validation of Common RP-HPLC Method for Estimation of Selected Triptans - Issue cover

Abstract

This paper describes the common analytical method suitable for the estimation of selected triptans (Naratriptan, Sumatriptan succinate, Zolmitriptan) by reversed phase high performance liquid chromatography (RP-HPLC). Chromatographic separations were conducted on Phenomenex Luna, C18 250 X 4.6 mm, 5 microns column at room temperature using 6.8 pH phosphate buffer: acetonitrile (60: 40) as a mobile phase at a flow rate of 1.0ml min-1, while UV detection was performed at 225nm. The retention time was found to be 3.130, 3.153, 2.143min respectively for the selected triptans. The method was found to be linear in the range of 2-10µg ml-1 for all the drugs. The proposed method is having good sensitivity due to low LOD and LOQ values. Analytical recovery was >99.3%. The method was validated statistically and applied for the quantitative analysis of triptans in bulk and formulations.

Authors (2)

K.Veditha

Vignan Pharmacy College, Vadla...

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T.E.G.K.Murthy

Bapatla College of Pharmacy, B...

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Article Information

AJPHR306017

AJPHR-30-000017

2015-06-01

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K.Veditha & T.E.G.K.Murthy (2015). Development and Validation of Common RP-HPLC Method for Estimation of Selected Triptans. American Journal of Pharmacy and Health Research, 3(6), xx-xx. https://ajphr.com/articles/AJPHR306017

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