Research Article | Volume : 1 Issue : 10, December 2011
Development of validated liquid chromatographic method for estimation of levocetirizine from pharmaceutical dosage forms
Open Access
Research Article | Volume : 1 Issue : 10, December 2011
Open Access
A simple and rapid high-performance liquid chromatographic (HPLC) method for the determination levocetirizine has been developed. The chromatographic system consisted of a Water 2695 binary gradient pump, Water 2487 dual wavelength absorbance detector, and Empower 2 software. Separation was achieved on the XTerra symmetry C18 column at room temperature. The sample was introduced through an injector valve with a 20 μL sample loop. The results obtained showed a good agreement with the declared content. Recovery values of levocetirizine in tablets were from 99.57-100.48 %. The proposed method is rapid, accurate and selective; it may be usedfor the quantitative analysis of levocetirizine from raw materials, in bulk drugs and other dosage formulations.
Year
Month
Formulation and Evaluation of Chitosan Beads of Levocetirizine Dihydrochloride
An unlimited scope for novel formulations as orally disintegrating systems: Present and future prospects
Reeta Rani Thakur, Mridul KashiRP HPLC Method for the determination of Tamsulosin in bulk and Pharmaceutical Formulations
Manish Kumar Thimmaraju, Venkat Rao, Hemanth .K, P. Siddartha Kumar