Design of fixed dose combination and physicochemical characterization of enteric-coated bilayer tablet with circadian rhythmic variations containing telmisartan and pravastatin sodium

2017 ◽  
Vol 523 (1) ◽  
pp. 343-356 ◽  
Author(s):  
Daoqi Luo ◽  
Joo Hee Kim ◽  
Chulhun Park ◽  
Euichaul Oh ◽  
Jun-Bom Park ◽  
...  
Author(s):  
Rajesh Desai ◽  
Suresh Koradia

The objective of this study is to isolation and characterization of unknown degradation product of Atorvastatin calcium in combination formulation product with Ezetimibe by using modern techniques of separation and aracterization. An unknown impurity is generating during a forced degradation study of Atorvastatin and Ezetimibe fixed-dose combination tablets. By using the gradient reversed-phase high-pressure liquid chromatographic method, unknown degradation impurity was detected and quantified in the range of 0.05% to 0.2% of Atorvastatin. The impurity was enriched by extreme oxidation degradation of Atorvastatin and isolated through preparative HPLC. The structure of the impurity was characterized by mass and NMR spectrum.


CrystEngComm ◽  
2018 ◽  
Vol 20 (21) ◽  
pp. 2923-2931 ◽  
Author(s):  
Srinivasulu Aitipamula ◽  
Joseph Cadden ◽  
Pui Shan Chow

A multi-API cocrystal containing two anti-obesity drugs, zonisamide and caffeine, was found to be promising for the development of a sustained release fixed-dose combination drug for the treatment of obesity.


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