VALIDATED RP-HPLC METHOD FOR QUANTITATION OF GLIQUIDONE IN PHARMACEUTICAL FORMULATION AND HUMAN SERUM
Author:
Publisher
SciELO Agencia Nacional de Investigacion y Desarrollo (ANID)
Subject
General Chemistry
Cited by 9 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Preparation and characterization for multicomponent crystals of the antidiabetic drug gliquidone based on crystal engineering;CrystEngComm;2019
2. Forced degradation of gliquidone and development of validated stability-indicating HPLC and TLC methods;Brazilian Journal of Pharmaceutical Sciences;2018-11-29
3. Stability Testing Followed by Manipulating Mean Centering Ratio and Derivative Ratio Spectrophotometric Methods for the Determination of Gliquidone in Presence of its Induced Degradation Products;Analytical Chemistry Letters;2018-05-04
4. Application of normal fluorescence and stability-indicating derivative synchronous fluorescence spectroscopy for the determination of gliquidone in presence of its fluorescent alkaline degradation product;Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy;2018-01
5. Determination of Serum Methylparaben Concentrations of Bangladeshi Breast Cancer Patients by RP-HPLC;Analytical Chemistry Letters;2017-09-03
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