Development of stability indicating reversed‐phase high‐performance liquid chromatography method for determination of elobixibat in pure form and laboratory prepared tablets: Application to dissolution study

Author:

Elagamy Samar H.1ORCID,Mansour Fotouh R.1,Elbastawissy Almoataz Bellah B.1,EL‐Malla Samah F.1

Affiliation:

1. Department of pharmaceutical analytical chemistry Faculty of Pharmacy Tanta University Tanta Egypt

Publisher

Wiley

Subject

Filtration and Separation,Analytical Chemistry

Reference31 articles.

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2. Forced degradation as an integral part of HPLC stability‐indicating method development;Ngwa G;Drug Deliv Technol.,2010

3. Current trends in forced degradation study for pharmaceutical product development;Singh R;J Pharm Educ Res.,2012

4. Fundamental chromatographic parameters;Ravisankar P;Int J Pharm Sci Rev Res,2019

5. Stability indicating RP‐HPLC method for determination of dimethyl fumarate in presence of its main degradation products: Application to degradation kinetics

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