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American Journal of PharmTech Research

Senthilkumar G.P

Author Profile
Bharathi College of Pharmacy, Bharathinagara.
2
Publications
2
Years Active
9
Collaborators
59
Citations

Publications by Senthilkumar G.P

2 publications found • Active 2011-2012

2012

1 publication

UV–SPECTROMETRIC DETERMINATION OF SORAFENIB TOSYLATE IN BULK AND PHARMACEUTICAL DOSAGE FORM

with Amol S. Powar, Pramila T, Tamizh Mani T, Parag S.Mahadik, Sandip B. Jagtap
2/1/2012

  A new, simple, economic and sensitive UV-spectrophotometric method was developed for the determination of Sorafenib in bulk and pharmaceutical formulations. The developed spectrometric method was validated for selectivity, linearity, range, precision, accuracy, ruggedness and sensitivity. The method has demonstrated excellent linearity over the range of 2-10 μg/ml with regression equation: y=0.079x-0.0081 and regression correlation coefficient r2=0.999. The developed method demonstrated consistent high recoveries (97–99%) and low relative standard deviation (< 5%) at 265 nm. Moreover, the method was found to be highly sensitive with low limit of detection (0.028 μg/ml) and limit of quantitation (0.085 μg/ml). The apparent molar absorptivity and Sandell's sensitivity was found to be 48.09 mol-1cm-1 and 0.013245 µg/cm2, respectively. The validated method was successfully employed for the drug content analysis from tablet preparations. Additionally, the method was also employed for pH metric solubility analysis of the drug.

2011

1 publication

SPECTROPHOTOMETRIC DETERMINATION OF CLOPIDOGREL BISULFATE IN PHARMACEUTICAL FORMULATIONS

with Suhas Gurav, Rohan Tembare, Vishali Salunkhe, Devprakash
12/1/2011

  A simple, sensitive and accurate spectrophotometric method was developed in ultraviolet region for the estimation of Clopidogrel bisulfate in pure drug, pharmaceutical formulation. Linear response obtained was in the concentration range of 25-50 µg/ml with correlation coefficient of 0.999 in 0.1 N HCl. Excellent recovery proved that the method was sufficiently accurate. There is no interference from any common pharmaceutical additives and diluents. Results of the analysis were validated by recovery studies according to ICH Q2B guidelines.  

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