Analytical ‘Quality-by-Design’ paradigm in development of a RP-HPLC method for the estimation of cilnidipine in nanoformulations: Forced degradation studies and mathematical modelling of in-vitro release studies-Reference-Cited by-同舟云学术

Analytical ‘Quality-by-Design’ paradigm in development of a RP-HPLC method for the estimation of cilnidipine in nanoformulations: Forced degradation studies and mathematical modelling of in-vitro release studies

Published:2023-10 Issue: Volume:193 Page:109124
ISSN:0026-265X
Container-title:Microchemical Journal
language:en
Short-container-title:Microchemical Journal

Author:

Miriam Marques Shirleen,Shirodkar Rupesh K.^ORCID,Kumar Lalit

Publisher

Elsevier BV

Subject

Spectroscopy,Analytical Chemistry

Reference52 articles.

1. Novel NP and RP-HPTLC in Praxis for Simultaneous Estimation of Chlorthalidone and Cilnidipine in Bulk and Pharmaceutical Formulation;Rathod;Anal. Chem. Lett.,2018

2. Comparative study of cilnidipine loaded PLGA nanoparticles: process optimization by DoE, physico-chemical characterization and in vivo evaluation;Diwan;Drug Deliv. Transl. Res.,2020

3. Fabrication of chitosan-alginate polyelectrolyte complexed hydrogel for controlled release of cilnidipine: a statistical design approach;Umaredkar;Mater. Technol.,2020

4. Investigation of inclusion complex of cilnidipine with hydroxypropyl-β-cyclodextrin;Hu;Carb. Polym.,2012

5. RP-HPLC In-Vitro Dissolution Method Development and Validation for Determination of Olmesartan Medoxomil, Chlorthalidone and Cilnidipine Drug Combinations;Shah;Curr. Pharm. Anal.,2022

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