Development and validation of a stability‐indicating, single HPLC method for sacubitril–valsartan and their stereoisomers and identification of forced degradation products using LC

Development and validation of a stability‐indicating, single HPLC method for sacubitril–valsartan and their stereoisomers and identification of forced degradation products using LC–MS/MS

Published:2022-12-07 Issue:2 Volume:37 Page:
ISSN:0269-3879
Container-title:Biomedical Chromatography
language:en
Short-container-title:Biomedical Chromatography

Author:

Vijaykumar Cholleti¹²^ORCID,Kumar Yalavarti Ravindra³,Aparna Pasula²,Rao Pydimarry Surya Prakash⁴

Affiliation:

1. Dr. Reddy's Laboratories Ltd, Active Pharmaceutical Ingredients, IPDO Hyderabad India

2. Department of Chemistry J.N.T. University Hyderabad India

3. RA Chem Pharma Ltd Hyderabad India

4. Analytical Research and Development, Hikma Pharmaceuticals USA Inc Columbus Ohio USA

Publisher

Wiley

Subject

Clinical Biochemistry,Drug Discovery,Pharmacology,Molecular Biology,General Medicine,Biochemistry,Analytical Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/bmc.5550

Reference35 articles.

1. Validation of a Capillary Electrophoresis Method for the Simultaneous Determination of Amlodipine Besylate and Valsartan in Pharmaceuticals and Human Plasma

2. Development of validated RP HPLC method with fluorescence detection for simultaneous quantification of sacubitril and valsartan from rat plasma

3. Stability‐indicating HPLC method development and validation of rivaroxaban impurities and identification of forced degradation products using LC–MS/MS

4. Development and validation of a reliable and rapid LC-MS/MS method for simultaneous quantification of sacubitril and valsartan in rat plasma and its application to a pharmacokinetic study

5. In vitro Dissolution Profile at Different Biological pH Conditions of Hydroxychloroquine Sulfate Tablets Is Available for the Treatment of COVID-19

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1. Simultaneous analysis of sacubitril and valsartan by novel analytical methods with green approach;Microchemical Journal;2024-04

2. Development of HPLC Method for Ixabepilone (Oncology Drug) in Bulk and Dosage Form: Quantification of Impurities and Forced Degradation Studies;Journal of Chromatographic Science;2023-07-18

3. A validated stability‐indicating reversed‐phase liquid chromatography method for the quantification of Ixabepilone (Oncology drug) in the parenteral dosage form;SEPARATION SCIENCE PLUS;2023-02-09