Determination of chemical stability of sitagliptin by LC-UV, LC-MS and FT-IR methods

Author:

Gumieniczek AnnaORCID,Berecka Anna,Mroczek Tomasz,Wojtanowski Krzysztof,Dąbrowska Kinga,Stępień Katarzyna

Publisher

Elsevier BV

Subject

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

Reference21 articles.

1. Diabetes treatment: the coming paradigm shift;Bloomgarden;J. Diabetes,2012

2. Development and validation of an HPLC method for the quantification of sitagliptin in plasma and tablet dosage forme;Ashraf;Lat. Am. J. Pharm,2015

3. Analytical method development and validation for some oral hypoglycemic drugs;Habibulla;Int. J. Pharm. Sci.,2014

4. Liquid chromatographic determination of sitagliptin either alone or in ternary mixture with metformin and sitagliptin degradation product;El-Bagary;Talanta,2011

5. A validated HPLC stability indicating method for the determination of sitagliptin in bulk drug substance and tablets;Qassas;Int. J Pharm Sci Rev Res,2015

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