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Vol. 1, Issue 10 (2012)

Development and Validation of HPTLC Method for Quantification of Silodosin in Bulk and Pharmaceutical Dosage Form

Author(s):
Sayana P. S., R. Shankar Iyer*, Shibi A., Harischandran S.
Abstract:
A simple, sensitive, precise and specific high-performance thin layer chromatographic method was developed and validated for the determination of silodosin in bulk and Pharmaceutical Dosage Forms. Validation was carried out in compliance with International Conference on Harmonization guidelines. The thin-layer chromatographic method employed aluminium plates precoated with silica gel 60 F254  as stationary phase. The solvent system consisted of toluene/methanol/diethylamine (8:1:1).This solvent system was found to give compact spot for silodosin with Rf value 0.37. Densitometric analysis of silodosin was carried in the fluorescence mode at 366 nm. Linear regression analysis showed good linearity with respect to peak area in the concentration range of 140-1400 ng per spot. The method was validated for precision, accuracy, specificity, and robustness.
Pages: 60-65  |  662 Views  11 Downloads
How to cite this article:
Sayana P. S., R. Shankar Iyer*, Shibi A., Harischandran S.. Development and Validation of HPTLC Method for Quantification of Silodosin in Bulk and Pharmaceutical Dosage Form. The Pharma Innovation Journal. 2012; 1(10): 60-65.
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