Stability‐indicating liquid chromatography method development and validation for impurity profiling of montelukast sodium in bulk drug and tablet dosage form-Reference-Cited by-同舟云学术

Stability‐indicating liquid chromatography method development and validation for impurity profiling of montelukast sodium in bulk drug and tablet dosage form

Published:2022-01-17 Issue:4 Volume:36 Page:
ISSN:0269-3879
Container-title:Biomedical Chromatography
language:en
Short-container-title:Biomedical Chromatography

Author:

Pasham Mohan¹^ORCID,Haridasyam Sharath Babu¹^ORCID,Boppy N. V. V. D. Praveen¹^ORCID,Venkatanarayana Muvvala¹^ORCID,Palakurthi Ashok Kumar²^ORCID

Affiliation:

1. Department of Chemistry GITAM Hyderabad Telangana India

2. Department of Analytical Research Aurex Laboratories LLC East Windsor NJ 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.5330

Reference31 articles.

1. Identification of potential impurities of montelukast imported to Syria by LC–MS and HPLC–UV;Aboulkhair M.;International Journal of Pharmaceutical Sciences Review and Research,2013

2. Development of a stability‐indicating hplc method for the determination of montelukast in tablets and human plasma and its applications to pharmacokinetic and stability studies;Alsarra I.;Saudi Pharmaceutical Journal,2004

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

4. Forced degradation and impurity profiling: Recent trends in analytical perspectives

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