original ) (raw )Degradation Pathway for Rilpinavir Hydrochloride by Validated Stability Indicating UP-LC Method
International Journal of Clinical Pharmacology & Toxicology (IJCPT)
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Development of Validated Stability-indicating RP-HPLC Method for Determination of Novel Directly Acting Antiviral agent and Characterization of its Degradants by LC–ESI–MS
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Indian Journal of Pharmaceutical Education and Research, 2020
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Emtricitabine, Tenofovir, and Rilpivirine from their degradation products Analysis by HPLC
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International Journal of Research in Pharmaceutical Sciences, 2019
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Development and Validation of Stability Indicating RP-HPLC Method for Estimation of Rilpivirine Hydrochloride in Tablet Dosage Form
Girija Bhavar
International Journal of Pharmaceutical Chemistry, 2014
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Analysis of Forced Degradation Products in Rilpivirine using RP-HPLC and Peak Purity Evaluation
Ramarao Abburi
Oriental journal of chemistry, 2023
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RP-HPLC Method Development and Validation for Simultanious Estimation and Forced Degradation Studies of Lamivudine and Raltegravir in Solid Dosage Form
SURENDRA LAGU
International Journal of Applied Pharmaceutics
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A new quantitative reverse phase high-performance liquid chromatographic method for the quantification of Rilpivirine hydrochloride in bulk and dosage form
Krishnaveni Nagappan
Journal of Applied Pharmaceutical Science, 2018
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Rilpivirine and Dolutegravir Simultaneously Measured via RP-HPLC-PDA with Box–Behnken Design Application: A Study of Forced Degradation under Various Conditions
shrouq H . sweilam
Separations, 2023
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Forced Degradation Studies and Development and Validation of HPLC-UV Method for the Analysis of Velpatasvir Copovidone Solid Dispersion
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Antibiotics
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RP-HPLC METHOD FOR SIMULTANEOUS ESTIMATION OF RITONAVIR, OMBITASVIR AND PARITAPREVIR IN TABLET DOSAGE FORMS AND THEIR STRESS DEGRADATION STUDIES Original Article
International Journal of Applied Pharmaceutics (IJAP)
International Journal of Applied Pharmaceutics, 2019
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Validated Stability-Indicating RP-HPLC Method for Daclatasvir in Tablets Short Title: Validated Stability-Indicating Method Daclatasvir by RP-HPLC
Hemlata Nimje , Meenakshi Deodhar
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Method Development and Validation of Assay of Rilpivirine in Rilpivirine Tablets by RP-HPLC
Mba I . Michael
2024
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ASSAY METHOD DEVELOPMENT AND VALIDATION OF CILNIDIPINE AND RAMIPRIL, CHARACTERIZATION OF ITS DEGRADANTS BY USING LC-MS/MS Original Article
International Journal of Applied Pharmaceutics (IJAP)
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Analytical Method Development and Validation and Forced Degradation Stability-Indicating Studies of Favipiravir by RP-HPLC and UV in Bulk and Pharmaceutical Dosage Form
Aejaz Ahmed
Journal of Pharmaceutical Research International
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A NEW ROBUST ANALYTICAL METHOD DEVELOPMENT, VALIDATION, AND STRESS DEGRADATION STUDIES FOR ESTIMATING RITONAVIR BY UV-SPECTROSCOPY AND HPLC METHODS Original Article
NEHA PARVEEN , AMIT KUMAR GOSWAMI , International Journal of Applied Pharmaceutics (IJAP)
International Journal of Applied Pharmaceutics, 2023
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A New Robust Analytical Method Development, Validation, and Stress Degradation Studies for Estimating Ritonavir by Uv-Spectroscopy and HPLC Methods
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Development & Validation of Stability Indicating HPTLC Method for Rilpivirine & Dolutegravir Sodium in Combination
Mrinalini Damle
2017
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Development and Validation of RP-HPLC Method for the Estimation of Dolutegravir and Rilpivirine in Bulk and its Tablet Dosage form
Tulja Rani
Journal of Pharmaceutical Research, 2021
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Reversed Phase LC-UV Method Development and Validation for Simultaneous determination of three antiretrovirals: Lamivudine, Zidovudine, Nevirapine and Possible Degradants in a Fixed Dose Pharmaceutical Product
Herbert Publications
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UPLC SEPARATION ANALYSIS OF EMTRICITABINE, TENOFOVIR, COBICISTAT AND ELVITEGRAVIR FROM THEIR DEGRADATION PRODUCTS
International Journal of Pharmacy and Pharmaceutical Sciences (IJPPS)
International Journal of Pharmacy and Pharmaceutical Sciences, 2016
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The Validation of a Simple, Robust, Stability-Indicating RP-HPLC Method for the Simultaneous Detection of Lamivudine, Tenofovir Disoproxil Fumarate, and Dolutegravir Sodium in Bulk Material and Pharmaceutical Formulations
Omobolanle A . Omoteso
International Journal of Analytical Chemistry, 2022
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RP-HPLC stability method development & validation for anti-HIV drugs cabotegravir & rilpivirine in I.M. injection and in human plasma
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International journal of health sciences
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Analytical methods for the quantification of ritonavir in pharmaceuticals, a comparative evaluation
ERTEN AKBEL
Bulletin of the Chemical Society of Ethiopia
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Identification of Degradation Products and a Stability-Indicating RP-HPLC Method for the Determination of Flupirtine Maleate in Pharmaceutical Dosage Forms
Ramalingam Peraman
2014
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A new validated stability-indicating RP-HPLC method for simultaneous quantification of dolutegravir and lamivudine in bulk and pharmaceutical dosage form
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Future Journal of Pharmaceutical Sciences, 2020
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Forced Degradation Study for Simultaneous Quantification of Aspirin and Omeprazole in Pharmaceutical Dosage form by RP-HPLC
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Development of Stability Indicating Assay Method for Separation and Identification of Degradation Products of Daclatasvir Dihydrochloride by LC-ESI-QTOF-MS/MS
Dr Debasish Swain
Analytical Chemistry Letters, 2019
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VALIDATED GRADIENT STABILITY INDICATING RP-HPLC METHOD FOR THE SIMULTANEOUS QUANTIFICATION OF 11 RELATED SUBSTANCES IN THE COMBINED DOSAGE FORMS OF LAMIVUDINE AND TENOFOVIR DISOPEOXIL FUMARATE
International Journal of Applied Pharmaceutics (IJAP)
International Journal of Applied Pharmaceutics, 2017
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AN INNOVATIVE METHOD DEVELOPMENT AND FORCED DEGRADATION STUDIES FOR SIMULTANEOUS ESTIMATION OF SOFOSBUVIR AND LEDIPASVIR BY RP HPLC Original Article
International Journal of Pharmacy and Pharmaceutical Sciences (IJPPS)
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Acta Chromatographica, 2016
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An Innovative Method Development and Forced Degradation Studies for Simultaneous Estimation of Sofosbuvir and Ledipasvir by RP HPLC
nazia khanam
International Journal of Pharmacy and Pharmaceutical Sciences, 2018
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Stability Indicating RP-HPLC Method Development and Validation for Simultaneous Estimation of Rivaroxaban and Clopidogrel Bisulphate in Pharmaceutical Dosage Form
Aejaz Ahmed
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Method Development and Validation of Rilpivirine in bulk and Pharmaceutical Tablet Dosage Form by using UV – Visible Spectrophometric Method
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Asian Journal of Research in Chemistry, 2012
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Validated stability indicating HPLC method to quantify lamivudine and dolutegravir in tablets
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International Journal of Research in Pharmaceutical Sciences
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