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Estimation of Piroxicam in Tablet Dosage Form by Using UV-Vis. Spectrophotometer


Affiliations
1 Department of Pharmaceutical Chemistry, Oriental College of Pharmacy, Bhopal, M.P., India
     

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A simple, accurate, sensitive and precise Ultraviolet spectrophotometric method has been developed for the determination of Piroxicam in tablet dosage form. The solutions of standard and sample were prepared in methanol. In the UV specrophotometric method, the quantitative determination of the drug was carried at 335 nm and the linearity range was found to be 2-12 μg/ml. The calibration graphs constructed at their wavelength of determination were found to be linear for specrophotometric methods. The proposed methods have been extensively validated statistically that included parameters such as linearity, accuracy, precision, LOD, LOQ, recovery and robustness. There was no significant difference between the performance of the proposed method regarding the mean values and standard deviations. The described methods can be readily utilized for analysis of pharmaceutical formulation.

Keywords

Method Development, Validation, Derivative Spectroscopy, Piroxicam.
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  • Estimation of Piroxicam in Tablet Dosage Form by Using UV-Vis. Spectrophotometer

Abstract Views: 186  |  PDF Views: 3

Authors

Sunil Singh
Department of Pharmaceutical Chemistry, Oriental College of Pharmacy, Bhopal, M.P., India
Jay Ram Patel
Department of Pharmaceutical Chemistry, Oriental College of Pharmacy, Bhopal, M.P., India
Sarita Kare
Department of Pharmaceutical Chemistry, Oriental College of Pharmacy, Bhopal, M.P., India

Abstract


A simple, accurate, sensitive and precise Ultraviolet spectrophotometric method has been developed for the determination of Piroxicam in tablet dosage form. The solutions of standard and sample were prepared in methanol. In the UV specrophotometric method, the quantitative determination of the drug was carried at 335 nm and the linearity range was found to be 2-12 μg/ml. The calibration graphs constructed at their wavelength of determination were found to be linear for specrophotometric methods. The proposed methods have been extensively validated statistically that included parameters such as linearity, accuracy, precision, LOD, LOQ, recovery and robustness. There was no significant difference between the performance of the proposed method regarding the mean values and standard deviations. The described methods can be readily utilized for analysis of pharmaceutical formulation.

Keywords


Method Development, Validation, Derivative Spectroscopy, Piroxicam.