Development and validation of a normal-phase HPTLC method for the simultaneous analysis of Lamivudine and Zidovudine in fixed-dose combination tablets-Reference-Cited by-同舟云学术

Development and validation of a normal-phase HPTLC method for the simultaneous analysis of Lamivudine and Zidovudine in fixed-dose combination tablets

Published:2012-04 Issue:2 Volume:2 Page:152-155
ISSN:2095-1779
Container-title:Journal of Pharmaceutical Analysis
language:en
Short-container-title:Journal of Pharmaceutical Analysis

Author:

Venkatesh Palani,Daggumati Mahesh

Publisher

Elsevier BV

Subject

Analytical Chemistry,Electrochemistry,Spectroscopy,Drug Discovery,Pharmaceutical Science,Pharmacy

Reference12 articles.

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2. Determination of 19 antiretroviral agents in pharmaceutical of suspected products with two methods using high performance liquid chromatography;Rebiere;J. Chromatogr. B,2007

3. Development and validation of RP-HPLC and ultraviolet spectrophotometric methods of analysis for the quantitative estimation of antiretroviral drugs in pharmaceutical dosage forms;Sarkar;J. Chromatogr. B,2006

4. Simultaneous determination of the HIV nucleoside analogue reverse transcriptase inhibitors lamivudine, didanosine, stavudine, zidovudine and abacavir in human plasma by reversed phase high performance liquid chromatography;Verweij-van Wissen;J. Chromatogr. B,2005

5. Simultaneous measurement of intracellular triphosphate metabolites of zidovudine, lamivudine and abacavir (carbovir) in human peripheral blood mononuclear cells by LC–MS;Brian;J. Chromatogr. B,2007

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