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American Journal of PharmTech Research

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HPTLC method Development, Validation for Simultaneous Determination of Efavirenz, Emtricitabine and Tenofovir in combined tablet formulation and Forced Degradation Studies

Published in February 2013 Issue 1 (Vol. 3, Issue 1, 2013)

HPTLC method Development, Validation for Simultaneous Determination of Efavirenz, Emtricitabine and Tenofovir in combined tablet formulation and Forced Degradation Studies - Issue cover

Abstract

A simple, sensitive, accurate and precise high performance thin layer chromatographic method was developed and validated for simultaneous determination of efavirenz (EFA), emtricitabine (EMT) and tenofovir (TEN) in combined tablet formulation and forced degradation studies were performed as per ICH guidelines. Precoated silica gel 60F 254 was used as stationary phase and the mobile phase used was chloroform: methanol (90:10), gives high resolution for each drug. The densitometric evaluation of each drug was carried out at 262 nm. The developed method was simple, accurate and is suitable for analysis of the drugs and degradation products in stability studies of samples.

Authors (3)

Nikalje Anna Pratima

Y.B. Chavan College of Pharmac...

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Maniyar Ajhar

Y.B. Chavan College of Pharmac...

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Obaid Shaikh

Y.B. Chavan College of Pharmac...

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Article Information

AJPTR31055

AJPTR-01-001576

2013-02-01

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How to Cite

Anna, N., & Ajhar & Shaikh (2013). HPTLC method Development, Validation for Simultaneous Determination of Efavirenz, Emtricitabine and Tenofovir in combined tablet formulation and Forced Degradation Studies. American Journal of PharmTech Research, 3(1), xx-xx. https://ajptr.com/articles/AJPTR31055

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