Development and Validation of Stability indicating UV Spectroscopic Method for Determination of Canagliflozin in Bulk and Pharmaceutical Dosage Form

2016 ◽  
Vol 7 (1) ◽  
pp. 63-69
Author(s):  
Ishpreet Kaur ◽  
Sharad Wakode ◽  
Harsharan Pal Singh
Author(s):  
VAIBHAV S KHODKE ◽  
GAME MD

Objective: The objective of the present study is to develop ultraviolet (UV)-spectroscopic method using pure drug and tablet dosage form that consistently produces a drug with a minimal variation that adheres to quality criteria of purity, identity, and potency. Methods: UV-spectrophotometric method has been developed using a solvent composed of methanol:water (30:70) as a diluent to determine the dalfampridine (DFP) content in bulk and pharmaceutical dosage form at predetermined λmax of 262 nm. Results: It was proved linear in the range of 02–12 μg/ml and exhibited a good correlation coefficient (r2 = 0.9915) and excellent mean recovery (0.004136347%). This method was successfully applied to the determination of DFP content of marketed tablet Dalstep 10 mg (Sun Pharmaceutical Pvt. Ltd.,) from India; the results were in good agreement with the label claims. Conclusion: The method proved to be simple, accurate, precise, specific, robust, and less time consuming and can be applied for the determination of DFP in bulk and marketed formulation.


2014 ◽  
Vol 77 (21-22) ◽  
pp. 1497-1501 ◽  
Author(s):  
Magdalena Paczkowska ◽  
Przemysław Zalewski ◽  
Piotr Garbacki ◽  
Alicja Talaczyńska ◽  
Anna Krause ◽  
...  

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