Cover image of the article: Reversed Phase High Performance Liquid Chromatographic Method for Determination of Quetiapine Fumarate in Pharmaceutical Formulation and in Spiked Human Urine

Image Credit:J Rep Pharm Sci

Reversed Phase High Performance Liquid Chromatographic Method for Determination of Quetiapine Fumarate in Pharmaceutical Formulation and in Spiked Human Urine

Authors

Kanakapura B Vinay1, Hosakere D Revanasiddappa1, Nagaraju Rajendraprasad2,*, Pavagada J Ramesh1, Kanakapura Basavaiah1
1Department of Chemistry, Manasagangothri, University of Mysore, Mysore-570 006, India
2PG Department of Chemistry, JSS College, Ooty Road, Mysore-570 025, India
*Corresponding Author: Corresponding author: PG Department of Chemistry, JSS College, Ooty Road, Mysore-570 025, India. Email:prasadtnpur@gmail.com

Journal of Reports in Pharmaceutical Sciences:Vol. 2, issue 2; 131-139
Published online:Sep 07, 2013
Article type:Research Article
Received:Aug 12, 2013
Accepted:Aug 26, 2013
How to Cite:Vinay KB, Revanasiddappa HD, Rajendraprasad N, Ramesh PJ, Basavaiah K. Reversed Phase High Performance Liquid Chromatographic Method for Determination of Quetiapine Fumarate in Pharmaceutical Formulation and in Spiked Human Urine. J Rep Pharm Sci. 2013;2(2):e147746. doi:

Abstract

A precise and feasible reversed-phase high-performance liquid chromatographic method for the determination of an antipsychotic drug quetiapine fumarate (QTF) in pharmaceuticals and spiked human urine sample has been developed and validated. The analysis was carried out using a ODS (250 mm × 4.6 mm i.d., 5 μm particle size) chromatopack column. Mobile phase containing a mixture of acetonitrile and 0.1% phosphate buffer (pH 3.1) (40:60) was pumped at a flow rate of 1 mL/min with UV detection at 240 nm at ambient column temperature (25 ºC). The method showed good linearity in the range of 0.09 – 18 μg/mL QTF with limits of detection (LOD) and quantification (LOQ) values of 0.03 and 0.09 μg/mL, respectively. The suggested method was successfully applied for the analysis of QTF in bulk drug, tablets and human urine with average recoveries of 100.06, 100.26 and 98.83%, respectively. The intra- and inter-day RSD values were less than 5%. The method is accurate, precise, sensitive and selective for routine analysis in quality control laboratories. 

Highlights

Copyright

© 2013, Author(s). This open-access article is available under the Creative Commons Attribution 4.0 (CC BY 4.0) International License (https://creativecommons.org/licenses/by/4.0/), which allows for unrestricted use, distribution, and reproduction in any medium, provided that the original work is properly cited.

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Kanakapura B VinayPubMedScholar
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Nagaraju RajendraprasadPubMedScholar
Pavagada J RameshPubMedScholar
Kanakapura BasavaiahPubMedScholar
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