Development of stability‐indicating method for separation and characterization of benidipine forced degradation products using LC–MS/MS-Reference-Cited by-同舟云学术

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Development of stability‐indicating method for separation and characterization of benidipine forced degradation products using LC–MS/MS

Published:2022-10-21 Issue:1 Volume:37 Page:
ISSN:0269-3879
Container-title:Biomedical Chromatography
language:en
Short-container-title:Biomedical Chromatography

Author:

Kushwah Bhoopendra Singh¹,Thummar Mohit M.¹,Yadav Amrej Singh¹,Dhiman Vivek¹,Samanthula Gananadhamu¹^ORCID

Affiliation:

1. Department of Pharmaceutical Analysis National Institute of Pharmaceutical Education and Research (NIPER) Hyderabad India

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.5517

Reference20 articles.

1. Identification, synthesis and characterization of process related impurities of benidipine hydrochloride, stress-testing/stability studies and HPLC/UPLC method validations

2. Development of forced degradation and stability indicating studies of drugs—A review

3. Isolation and characterization of novel degradation products in cilnidipine by LC-QTOF-MS/MS, LCMSn, 2D-NMR and FTIR

4. Chromatographic approaches for the characterization and quality control of therapeutic oligonucleotide impurities

5. ICH Q1B;ICH;Stability Testing: Photostability Testing of New Drug Substances and Products,1996

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1. Impurities in Active Pharmaceutical Ingredients and Drug Products: A Critical Review;Critical Reviews in Analytical Chemistry;2024-07-26

2. Combined green analytical principles and quality by design for ultraperformance liquid chromatography analytical method development, the characterization and in-silico toxicity prediction of Ixazomib degradation products using mass spectrometry;Green Analytical Chemistry;2024-03

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