original ) (raw )Review: Development of forced degradation studies of drugs
Scholar Science Journals
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The use of liquid chromatography±mass spectrometry for the identi®cation of drug degradation products in pharmaceutical formulations
Marco Garzotti
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Current Trend in Performance of Forced Degradation Studies for Drug Substance and Drug Product’s
Rajveer Bhaskar
Journal of Drug Delivery and Therapeutics
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Development of forced degradation and stability indicating studies of drugs—A review
Dr. Prajesh Prajapati
Journal of Pharmaceutical Analysis, 2014
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Forced Degradation Study: An Important Tool in Drug Development AB Roge, PS Tarte, MM Kumare, Dr. G R Shendarkar, Dr. S M Vadvalkar
Mangesh Kumare
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A NOVEL STABILITY-INDICATING RP-UPLC METHOD FOR THE QUANTIFICATION OF IMPURITIES AND A NEW QDa MASS DETECTOR COUPLED WITH LC-PDA FOR IDENTIFICATION OF MASS OF DEGRADATION PRODUCTS IN A FIXED DOSE COMBINATION OF EMPAGLIFLOZIN AND LANIGLIPTIN TABLETS USED AS SECOND-LINE THERAPY FOR TYPE-2 DIABETES
varaprasad jagadabi
International Research Journal of Pharmacy, 2018
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Kinetic Degradation Study of Dapagliflozin Coupled with UHPLC Separation in the Presence of Major Degradation Product and Metformin
Wafaa A Zaghary
Chromatographia, 2019
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Author's Accepted Manuscript Development of forced degradation and stability indicating studies of drugs – A review
yang gattuso
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An Introduction to Forced degradation studies for drug substances and drug products
MUSKAN singh
Journal of emerging technologies and innovative research, 2021
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Technical Considerations of Forced Degradation Studies of New Drug Substances and Product: Regulatory Perspectives
Parul Singh
Journal of Drug Delivery and Therapeutics, 2018
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Forced degradation study of efonidipine HCl ethanolate, characterization of degradation products by LC-Q-TOF-MS and NMR
Charu Pandya
Journal of Applied Pharmaceutical Science, 2020
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Strategy for identification and characterization of small quantities of drug degradation products using LC and LC-MS: Application to valsartan, a model drug
Saranjit Singh
Drug Testing and Analysis, 2010
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Novel validated stability-indicating UPLC method for the determination of Metoclopramide and its degradation impurities in API and pharmaceutical dosage form Prathyusha Sowjanya a,*, Palani Shanmugasundaram , Petla Naidu , Sanjeev Kumar Singamsetty
Palani Shanmugasundaram
journal of pharmacy research 6 (2013) 765 e773, 2013
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A review article – development of forced degradation and stability indicating studies for drug substance and drug product
IJRPP Journal
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IDENTIFICATION OF DABIGATRAN ETEXILATE MAJOR DEGRADATION PATHWAYS BY LIQUID CHROMATOGRAPHY COUPLED TO MULTI STAGE HIGH-RESOLUTION MASS SPECTROMETRY
caroline chodur
RSC Adv., 2015
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Stress Degradation Behavior of Desipramine Hydrochloride and Development of Suitable Stability-Indicating LC Method
Girish Deshpande
Chromatographia, 2008
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Characterization of forced degradation products of ketorolac tromethamine using LC/ESI/Q/TOF/MS/MS and in silico toxicity prediction
Divya Dornala
Journal of Mass Spectrometry, 2014
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Forced degradation of nepafenac: Development and validation of stability indicating UHPLC method
Irena Nekola
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New Validated RP-HPLC Method for Quantification of Rupatadine FumarateImpurities in Solid Dosage Form Supported By Forced Degradation Studies
Rajan Rele
Der Pharmacia Lettre, 2016
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Chromatographic separation of tiropramide hydrochloride and its degradation products along with their structural characterization using LC-QTOF-MS/MS and NMR
Bhoopendra Singh Kushwah
Research Square (Research Square), 2022
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Forced degradation studies for Drug Substances and Drug Products-Scientific and Regulatory Considerations
Kumar Sourabh Jain
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Systematic strategies for degradation kinetic study of pharmaceuticals: an issue of utmost importance concerning current stability analysis practices
Tarang Jadav
Journal of Analytical Science and Technology, 2022
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In vitro Comparative Degradation Study of Different Brands of Domperidone Using UV Spectrophotometer
Abul Hasanat
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Forced Degradation Study for Simultaneous Quantification of Aspirin and Omeprazole in Pharmaceutical Dosage form by RP-HPLC
chandni chandarana
Journal of Pharmaceutical Research International
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ANALYTICAL ASSAY METHOD VALIDATION AND FORCED DEGRADATION BEHAVIOR OF S (-) AMLODIPINE BESILATE AND LOSARTAN POTASSIUM FROM FIXED DOSE COMBINATION
INTERNATIONAL JOURNAL
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Development and validation of a stability-indicating RP-HPLC method for the identification, determination of related substances and assay of dimethyl fumarate in drug substance
Samit Kumar
Annales Pharmaceutiques Françaises, 2021
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Structural elucidation of degradation products of a benzopyridooxathiazepine under stress conditions using electrospray orbitrap mass spectrometry – Study of degradation kinetic
Jean-françois Goossens
European Journal of Pharmaceutical Sciences, 2012
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Identification of Degradation Products in Cyclophosphamide API by LC-QTOF Mass Spectrometry Identification of Degradation Products in Cyclophosphamide API by LC-QTOF Mass Spectrometry
shiva gudlawar
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DEVELOPMENT AND VALIDATION OF A STABILITY-INDICATING RELATED SUBSTANCES OF TRANDOLAPRIL BY RP-HPLC AND ITS DEGRADATION Original Article
International Journal of Applied Pharmaceutics (IJAP)
International Journal of Applied Pharmaceutics, 2021
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Quality Control Assessment of Dutasteride and Silodosin in Capsules and Tablets Employing a Novel Developed HPLC Technique; Evaluation of Stabilities of Dutasteride and Silodosin in Accelerated Degradation
Balaji Gupta Tiruveedhi
International Journal of Applied Pharmaceutics, 2023
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QUALITY CONTROL ASSESSMENT OF DUTASTERIDE AND SILODOSIN IN CAPSULES AND TABLETS EMPLOYING A NOVEL DEVELOPED HPLC TECHNIQUE; EVALUATION OF STABILITIES OF DUTASTERIDE AND SILODOSIN IN ACCELERATED DEGRADATION Original Article
International Journal of Applied Pharmaceutics (IJAP)
International Journal of Applied Pharmaceutics, 2023
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Forced degradation studies of lansoprazole using LC-ESI HRMS and 1 H-NMR experiments: in vitro toxicity evaluation of major degradation products
Nagesh Narayana
Journal of Mass Spectrometry, 2017
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Impurity profiling of trandolapril under stress testing: Structure elucidation of by-products and development of degradation pathway
Maha Dendeni
International journal of pharmaceutics, 2012
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LC-MS/MS Characterization of Forced Degradation Products of Repaglinide Quality by Design Approach for Stability-Indicating LC Method Development and Validation for Degradation Products
Saeed Albaseer
Analytical Chemistry Letters, 2020
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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)
International Journal of Applied Pharmaceutics, 2022
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