Stability‐indicating RP‐HPLC method development and validation for determination of nine impurities in apixaban tablet dosage forms. Robustness study by quality by design approach-Reference-Cited by-同舟云学术

Stability‐indicating RP‐HPLC method development and validation for determination of nine impurities in apixaban tablet dosage forms. Robustness study by quality by design approach

Published:2019-11-19 Issue:1 Volume:34 Page:
ISSN:0269-3879
Container-title:Biomedical Chromatography
language:en
Short-container-title:Biomedical Chromatography

Author:

Subramanian Velusamy B.¹,Katari Naresh Kumar¹²^ORCID,Dongala Thirupathi³^ORCID,Jonnalagadda Sreekantha B.²^ORCID

Affiliation:

1. Department of Chemistry, School of ScienceGITAM deemed to be University Hyderabad Medak Telangana India

2. Aurex Laboratories LLC East Windsor NJ USA

3. School of Chemistry and Physics, College of Agriculture, Engineering and Science, Westville CampusUniversity of KwaZulu–Natal Durban South Africa

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.4719

Reference25 articles.

1. Oral Apixaban for the Treatment of Acute Venous Thromboembolism

2. Apixaban with Antiplatelet Therapy after Acute Coronary Syndrome

3. Application of quality by design elements for the development and optimization of an analytical method for protamine sulfate

4. Validation of an LC–MS/MS method for the simultaneous quantification of dabigatran, rivaroxaban and apixaban in human plasma

5. Apixaban in Patients with Atrial Fibrillation

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