Identification, isolation and characterization of dolutegravir forced degradation products and their cytotoxicity potential

SJ Saida, A Manikandan, M Kaliyaperumal… - … of pharmaceutical and …, 2019 - Elsevier
Dolutegravir was approved by USFDA, Canada and European regulatory authorities as
antiretroviral medication. In this article, DLG forced degradation studies as per the …

A simple stability indicating RP-HPLC-dad method for concurrent analysis of tenofovir disoproxil fumarate, doravirine and lamivudine in pure blend and their combined …

R Godela, S Gummadi - Annales Pharmaceutiques Françaises, 2021 - Elsevier
Objectives The main aim of the study was to develop an economical, insightful, accurate and
simple RP-HPLC-DAD method with high precision and good sensitivity for concurrent …

A new stability indicating RP-UPLC method for simultaneous estimation of Doravirine, Lamivudine and Tenofovir disoproxil fumarate in bulk and their combined …

S Addanki, BR Kuber - Future Journal of Pharmaceutical Sciences, 2021 - Springer
Background To establish a simple, sensitive, accurate, precise, efficient, economical RP-
UPLC method for simultaneous estimation of Doravirine, Lamivudine and Tenofovir …

HPLC-MS identification of acid degradation products of dolutegravir

S Krait, DK Wissenbach, FT Peters… - Journal of Pharmaceutical …, 2021 - Elsevier
Dolutegravir is an integrase strand transfer inhibitor used for the treatment of human immuno-
deficiency virus infections. The present study was conducted in order to identify degradation …

A new Stability-indicating UHPLC for the simultaneous determination of a combination of Anti-viral drugs: Dolutegravir sodium, Lamivudine and Tenofovir disoproxil …

AK Kota, MM Annapurna - Research Journal of Pharmacy and …, 2022 - indianjournals.com
Dolutegravir sodium, Lamivudine and Tenofovir disoproxil fumarate are anti-viral drugs. A
new stability indicating UHPLC method has been proposed for the simultaneous …

Concurrent estimation of lamivudine, tenofovir disoproxil fumarate, and efavirenz in blended mixture and triple combination tablet formulation by a new stability …

R Godela, V Kammari, S Gummadi, D Beda - Future Journal of …, 2021 - Springer
Background An easy, defined, rapid, and accurate reverse phase high-performance liquid
chromatography method was developed and subsequently validated for the concurrent …