Table of Contents Author Guidelines Submit a Manuscript
International Journal of Analytical Chemistry
Volume 2011, Article ID 729651, 8 pages
Research Article

A New Spectrophotometric Method for Determination of Selenium in Cosmetic and Pharmaceutical Preparations after Preconcentration with Cloud Point Extraction

1Department of Analytical Chemistry, Faculty of Chemistry, Tabriz University, Tabriz 51664-14766, Iran
2Department of Chemistry, Faculty of Science, Islamic Azad University, Khorramabad Branch, Khorramabad, Iran
3Department of Analytical Chemistry, Faculty of Chemistry, Razi University, Kermanshah, Iran

Received 18 May 2010; Revised 5 December 2010; Accepted 8 February 2011

Academic Editor: Richard G. Brereton

Copyright © 2011 Mohammad Hosein Soruraddin et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.


A simple, rapid, and sensitive spectrophotometric method for the determination of trace amounts of selenium (IV) was described. In this method, all selenium spices reduced to selenium (IV) using 6 M HCl. Cloud point extraction was applied as a preconcentration method for spectrophotometric determination of selenium (IV) in aqueous solution. The proposed method is based on the complexation of Selenium (IV) with dithizone at pH < 1 in micellar medium (Triton X-100). After complexation with dithizone, the analyte was quantitatively extracted to the surfactant-rich phase by centrifugation and diluted to 5 mL with methanol. Since the absorption maxima of the complex (424 nm) and dithizone (434 nm) overlap, hence, the corrected absorbance, Acorr, was used to overcome the problem. With regard to the preconcentration, the tested parameters were the pH of the extraction, the concentration of the surfactant, the concentration of dithizone, and equilibration temperature and time. The detection limit is 4.4 ng mL-1; the relative standard deviation for six replicate measurements is 2.18% for 50 ng mL-1 of selenium. The procedure was applied successfully to the determination of selenium in two kinds of pharmaceutical samples.