Green sustainable assessment of stability indicating first derivative synchronous fluorimetry for determination of anti-diabetic drug with its toxic impurity

Author:

Nabil Nada,Sedik Ghada A.,Zaazaa Hala E.,El-Mosallamy Sally S.ORCID

Publisher

Elsevier BV

Subject

Management, Monitoring, Policy and Law,Pharmaceutical Science,Pollution,Environmental Chemistry

Reference30 articles.

1. Quantitative determination of canagliflozin in human plasma samples using a validated HPTLC method and its application to a pharmacokinetic study in rats;Alam;Biomed. Chromatogr.,2020

2. A rapid RP-HPLC method for the simultaneous estimation of Ivacaftor and Tezacaftor and in silico study of their metabolitic products;Donakonda;Futur J Pharm Sci,2021

3. Stability indicating 1st derivative synchronous spectrofluorimetric method for the determination of the newly approved antiviral drug daclatasvir in presence of its oxidative and photolytic degradation products: application to tablet dosage form;El-Gamal;Pharm. Anal. Acta,2018

4. Zero and second-derivative synchronous fluorescence spectroscopy for the quantification of two non-classical β-lactams in pharmaceutical vials: application to stability studies;Elzanfaly;Luminescence,2017

5. Canagliflozin stability study and ecofriendly chromatographic determination of its degradation product: a comparative study;Emam;J. Separ. Sci.,2018

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