Stability indicating RP-HPLC method for the determination of Atazanavir sulphate in bulk and dosage form
CH Bhirud, SN Hiremath - Drug Invention Today, 2013 - Elsevier
Objective The objective of the present work is to develop a simple, precise, accurate,
validated stability indicating RP-HPLC method for the determination of Atazanavir sulphate …
validated stability indicating RP-HPLC method for the determination of Atazanavir sulphate …
Simultaneous determination of impurities of atazanavir and ritonavir in tablet dosage form by using reversed-phase ultra performance liquid chromatographic method
MKVVN Mantripragada, SV Rao… - Journal of …, 2018 - academic.oup.com
A simple, rapid, selective and stability indicating reversed phase-ultra performance liquid
chromatography method was developed and validated for the simultaneous quantification of …
chromatography method was developed and validated for the simultaneous quantification of …
[PDF][PDF] Identification, Separation and Characterization of Acidic and Oxide Degradation of Atazanavir Sulphate Under ICH-Recommended Stress Conditions by HPTLC …
P Patil, S Bagde, K Kalad… - International …, 2024 - jourdata.s3.us-west-2.amazonaws …
Background: Studies have indicated that atazanavir is prone to degradation in environments
with high levels of acidity and oxidative stress. However, the drug demonstrated stability …
with high levels of acidity and oxidative stress. However, the drug demonstrated stability …
Analytical Techniques for the Analysis of Lopinavir and Ritonavir in Pharmaceutical Dosage Form and Biological Matrices: A Review
M Amir, P Narula, F Bano - Current Pharmaceutical Analysis, 2022 - ingentaconnect.com
Background: Lopinavir and Ritonavir are protease inhibitor type of anti-retroviral drugs. Both
are used for the treatment of HIV/AIDS. This paper reviews many analytical methods for the …
are used for the treatment of HIV/AIDS. This paper reviews many analytical methods for the …
[PDF][PDF] International Journal of Lifescience and Pharma Research
A Patchala, R Nadendla - researchgate.net
A fixed oral dose combination of Atazanavir and Ritonavir is currently used for the treatment
of patients with HIV infections. A selective and novel bio-analytical technique was designed …
of patients with HIV infections. A selective and novel bio-analytical technique was designed …
[PDF][PDF] World Journal of Pharmaceutical Sciences
PL Madhuri, DG Sankar - academia.edu
ABSTRACT A simple, speedy, sensitive, accurate and validated isocratic RP-HPLC/UV bio
analytical method was developed for the concurrent quantitative estimation of atazanavir …
analytical method was developed for the concurrent quantitative estimation of atazanavir …
[PDF][PDF] Development and Valida Atazanavir in Synthetic Mixture
S Ganta - AJ Chem - academia.edu
ABSTRACT A simple accurate and selective Rp-HPLC Cobicistat (COB) and Atazanavir
(ATA) 4.6 mm) with reverse phase elution of the mobil orthophosphoric acid: MeOH (30 …
(ATA) 4.6 mm) with reverse phase elution of the mobil orthophosphoric acid: MeOH (30 …
[PDF][PDF] SIMULTANIOUS ESTIMATION OF COBICISTAT AND ATAZANAVIR SULPHATE IN BULK AND COMBINED DOSAGE FORM BY UV-SPECTROPHOTOMETRIC …
BV Purnima, MS Kumari, G Ramu, TVB Reddy… - 2016 - wjpr.s3.ap-south-1.amazonaws.com
ABSTRACT A simple and sensitive ultra-violet spectrophotometric method was developed
and validated for the determination of cobicistat (COBI) and atazanavir sulphate (ATV) …
and validated for the determination of cobicistat (COBI) and atazanavir sulphate (ATV) …
[引用][C] Validated Stability-Indicating Liquid Chromatographic Method for the Determination of Atazanavir sulpahte (Anti-Retroviral Agent) in Capsules
G Sowjanya, MS Chandra, JS Rao - Journal of Chemical and Pharmaceutical …, 2015