Please use this identifier to cite or link to this item: http://hdl.handle.net/10553/47154
Title: Microwave-assisted micellar extraction coupled with solid-phase extraction for preconcentration of pharmaceuticals in molluscs prior to determination by HPLC
Authors: Cueva-Mestanza, R.
Torres-Padrón, M. E. 
Sosa-Ferrera, Z. 
Santana-Rodriguez, J. J. 
UNESCO Clasification: 2301 química analítica
2391 Química ambiental
Keywords: Pharmaceutical residues
Molluscs
Microwave-assisted micellar extractio
Solid-phase extractio
HPLC-UV-DAD
Issue Date: 2008
Publisher: 0269-3879
Project: Acoplamiento de la Microextracción en Fase Sólida y la Cromatografía Líquida de Alta Resolución Con la Utilización de Medios Micelares Como Extractantes: Desarrollo de Nuevos Métodos Analíticos 
Journal: Biomedical Chromatography 
Abstract: A simple and specific analytical method was developed and tested for the determination of pharmaceuticals in mollusc samples. A combination of microwave‐assisted micellar extraction (MAME) and solid‐phase extraction (SPE) using a non‐ionic surfactant, polyoxyethylene 10 lauryl ether, was examined to extract and determine simultaneously a group of pharmaceuticals such as carbamazepine, clorfibric acid, ketoprofen, naproxen, bezafibrate and ibuprofen by liquid chromatography using UV‐diode array detector. The MAME extraction performance was evaluated by studying various parameters such as the volume and concentration of surfactant and microwave conditions. Finally, an OASIS HLB cartridge was used as an optimum SPE sorbent to clean up the extracts and preconcentrate the selected analytes. The proposed method showed satisfactory linearity and reproducibility (between 3 and 15%), as well as detection limits ranging from 30 to 220 ng/g. Finally, the method was successfully applied to the determination of the target pharmaceuticals in various kinds of mollusc samples. This study has demonstrated that microwave‐assisted micellar extraction with solid‐phase extraction may be used as a viable alternative to conventional methods for the extraction of pharmaceuticals in this type of matrices.
URI: http://hdl.handle.net/10553/47154
ISSN: 0269-3879
DOI: 10.1002/bmc.1033
Source: Biomedical Chromatography [ISSN 0269-3879], v. 22, p. 1115-1122
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