Development of an analytical method for the determination of pimavanserin and its impurities applying analytical quality by design principles as a risk-based strategy-Reference-Cited by-同舟云学术

Development of an analytical method for the determination of pimavanserin and its impurities applying analytical quality by design principles as a risk-based strategy

Published:2021-07 Issue: Volume:201 Page:114091
ISSN:0731-7085
Container-title:Journal of Pharmaceutical and Biomedical Analysis
language:en
Short-container-title:Journal of Pharmaceutical and Biomedical Analysis

Author:

Radić Irena,Runje Mislav,Babić Sandra^ORCID

Publisher

Elsevier BV

Subject

Clinical Biochemistry,Spectroscopy,Drug Discovery,Pharmaceutical Science,Analytical Chemistry

Reference29 articles.

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3. Development of a UPLC–MS/MS method for determination of pimavanserin tartrate in rat plasma: application to a pharmacokinetic study;Wang;J. Pharm. Anal.,2017

4. Quantification of pimavanserin in bulk and tablet dosage form using a stability indicating high performance liquid chromatographic method;Koduri;Pharm. Sci.,2018

5. Application of quality by design to the development of analytical separation methods;Orlandini;Anal. Bioanal. Chem.,2013

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