Forced degradation of gliquidone and development of validated stability-indicating HPLC and TLC methods

Author:

El-ghobashy Mohamed Refaat1,Yehia Ali Mohamed1,Helmy Aya Helmy2,Youssef Nadia Fayek2

Affiliation:

1. Cairo University, Egypt

2. National Organization for Drug Control and Research, Egypt

Publisher

FapUNIFESP (SciELO)

Reference18 articles.

1. Basic statistics;Agarwal BL,2013

2. High-performance Liquid Chromatographic analysis of pioglitazone, gliquidone, rosuvastatin and simvastatin in formulations and human serum;Arayne MS;Chin J Chem,2010

3. Spectrophotometric method for quantitative determination of gliquidone in bulk drug, pharmaceutical formulations and human serum;Arayne MS;Pak J Pharm Sci,2006

4. Validated RP-HPLC method for quantification of gliquidone in pharmaceutical formulation and human serum;Arayne MS;J Chil Chem Soc,2010

5. Matindale The complete drug reference;Brayfield A,2014

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