Quality by design with design of experiments approach for development of a stability‐indicating LC method for enzalutamide and its impurities in soft gel dosage formulation-Reference-Cited by-同舟云学术

Quality by design with design of experiments approach for development of a stability‐indicating LC method for enzalutamide and its impurities in soft gel dosage formulation

Published:2021-02-08 Issue:5 Volume:35 Page:
ISSN:0269-3879
Container-title:Biomedical Chromatography
language:en
Short-container-title:Biomedical Chromatography

Author:

Katakam Lakshmi Narasimha Rao¹,Dongala Thirupathi²^ORCID,Ettaboina Santhosh Kumar²

Affiliation:

1. Department of Chemistry JNTU Hyderabad Telangana India

2. Quality control Aurex Laboratories LLC East Windsor New Jersey 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.5062

Reference30 articles.

1. A validated stability indicating RP‐HPLC method development for anticancer drug enzalutamide in bulk and pharmaceuticals;Anjaneyulu Reddy B.;International Journal of Pharmaceutical Sciences and Drug Research,2019

2. QbD based development of HPLC method for simultaneous quantification of Telmisartan and hydrochlorothiazide impurities in tablets dosage form;Ashok K. P.;Practical Laboratory Medicine,2020

3. Validation of a method for quantifying enzalutamide and its major metabolites in human plasma by LC–MS/MS

4. Enzalutamide and analytical interferences in digoxin assays

5. Development and validation of RP‐HPLC method for simultaneous determination of diclofenac potassium and its process related impurities in solid Oral dosage form;Dongala T.;Journal of Chromatography and Separation Techniques,2018

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