In the pharmaceutical industry, effective risk management and control strategies for potential
genotoxic impurities are of paramount importance. The current study utilized GC–MS to …

In this paper, for the first time, the study of electrochemical investigation and voltammetric
determination of HIV integrase inhibitor dolutegravir was described. The effect of …

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 …

The present study was aimed to develop and validate simple, sensitive, precise, economic
and accurate method for simultaneous estimation of Lamivudine and Dolutegravir Sodium in …

Background To establish a simple, sensitive, accurate, precise, efficient, economical RP-
UPLC method for simultaneous estimation of Doravirine, Lamivudine and Tenofovir …

This study describes the development of a reliable and linear analytical method for precisely
determining dimethylamine impurity in N, N‐dimethylformamide solvent utilizing a benzoyl …

In the analysis of the pharmaceutical agents new sophisticated chromatographic methods
have been utilized for the quality control purpose. In the current scenario ample amount of …

Dolutegravir sodium, Lamivudine and Tenofovir disoproxil fumarate are anti-viral drugs. A
new stability indicating UHPLC method has been proposed for the simultaneous …

Objective The purpose of this research was to develop and validate a stability-indicating RP–
HPLC technique for simultaneous quantification of Emtricitabine (EMT), Tenofovir …

Background An easy, defined, rapid, and accurate reverse phase high-performance liquid
chromatography method was developed and subsequently validated for the concurrent …