Development and optimization of liquid chromatography analytical methods by using AQbD principles: Overview and recent advances

T Tome, N Žigart, Z Časar… - Organic process research …, 2019 - ACS Publications
This review presents the Analytical Quality by Design (AQbD) concept, an extension of
Quality by Design (QbD), which was introduced in 2004 by the US Food and Drug …

Innovative molecularly imprinted electrochemical sensor for the nanomolar detection of Tenofovir as an anti-HIV drug

M Mehmandoust, M Soylak, N Erk - Talanta, 2023 - Elsevier
Tenofovir (TNF) is an antiviral medicine that is utilized to treat the human immunodeficiency
virus (HIV). However, its level must be controlled in the human body and environment at the …

A concise analytical profile of efavirenz: analytical methodologies

JP Ambhore, SR Chaudhari, RS Cheke… - Critical Reviews in …, 2022 - Taylor & Francis
Non-nucleoside reverse transcriptase inhibitors are the prime members of antiretroviral
therapy that are presently employed for the management of the human immunodeficiency …

Development and validation of reverse-phase high-performance liquid chromatographic (RP-HPLC) method for quantification of Efavirenz in Efavirenz-Enfuvirtide co …

DH Surve, AB Jindal - Journal of Pharmaceutical and Biomedical Analysis, 2019 - Elsevier
The objective of present work was to develop rapid, sensitive, selective, accurate and
precise RP-HPLC method for analysis of Efavirenz from combination anti-HIV drug …

Simultaneous spectrophotometric method for determination of emtricitabine and tenofovir disoproxil fumarate in three‐component tablet formulation containing …

S Venkatesan, N Kannappan - International scholarly research …, 2014 - Wiley Online Library
Developing a single analytical method for estimation of individual drug from a multidrug
composition is a very challenging task. A complexation, derivatization, extraction …

Quantification and validation of stability-indicating RP-HPLC method for efavirenz in bulk and tablet dosage form using quality by design (QbD): A shifting paradigm

VC Gurumukhi, SB Bari - Journal of Chromatographic Science, 2022 - academic.oup.com
The present study endeavors quality by design (QbD) assisted chromatographic method for
the quantification of Efavirenz (ERZ) in bulk and tablet dosage form. Analytical QbD …

[PDF][PDF] A review on forced degradation studies, stability indicating method and stability profile of few antiviral drugs

K Somase, D Rishipathak - Journal of Pharmaceutical Negative …, 2022 - pnrjournal.com
The aim of the study is to provide with available literature on regulatory aspects and
protocols for forced degradation investigations and stability indicating methods of various …

A Rapid Reversed‐Phase HPLC Method for Analysis of Trans‐Resveratrol in PLGA Nanoparticulate Formulation

G Singh, RS Pai - International Scholarly Research Notices, 2014 - Wiley Online Library
A rapid reversed‐phase high performance liquid chromatography (RP‐HPLC) method was
developed for the determination of trans‐resveratrol (t‐RVT) in PLGA nanoparticle …

Optimization (Central Composite Design) and Validation of HPLC Method for Investigation of Emtricitabine Loaded Poly(lactic‐co‐glycolic acid) Nanoparticles: In Vitro Drug …

G Singh, RS Pai - The Scientific World Journal, 2014 - Wiley Online Library
The objective of the current study is to develop nanoparticles (NPs) drug delivery system of
emtricitabine solely using poly (lactic‐co‐glycolic acid)(PLGA) and evaluate its in vitro and in …

Stability behaviour of antiretroviral drugs and their combinations. 3: Characterization of interaction products of emtricitabine and tenofovir disoproxil fumarate by mass …

M Kurmi, DK Singh, S Tiwari, P Sharma… - Journal of Pharmaceutical …, 2016 - Elsevier
The present study investigated drug–drug interaction behaviour of emtricitabine (FTC) and
tenofovir disoproxil fumarate (TDF) under solid state stability test conditions. Six interaction …