Cueva-Mestanza R, Torres-Padrón M E, Sosa-Ferrera Z, Santana-Rodríguez J J
Department of Chemistry, Faculty of Marine Sciences, University of Las Palmas de Gran Canaria, 35017 Las Palmas de Gran Canaria, Spain.
Biomed Chromatogr. 2008 Oct;22(10):1115-22. doi: 10.1002/bmc.1033.
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.
开发并测试了一种简单且特异的分析方法,用于测定软体动物样本中的药物。研究了采用非离子表面活性剂聚氧乙烯10月桂醚的微波辅助胶束萃取(MAME)和固相萃取(SPE)相结合的方法,通过使用紫外二极管阵列检测器的液相色谱法同时萃取和测定一组药物,如卡马西平、氯贝酸、酮洛芬、萘普生、苯扎贝特和布洛芬。通过研究各种参数,如表面活性剂的体积和浓度以及微波条件,评估了MAME萃取性能。最后,使用OASIS HLB柱作为最佳的SPE吸附剂来净化提取物并对选定的分析物进行预浓缩。所提出的方法显示出令人满意的线性和重现性(3%至15%之间),以及30至220 ng/g的检测限。最后,该方法成功应用于测定各种软体动物样本中的目标药物。本研究表明,微波辅助胶束萃取与固相萃取相结合可作为这类基质中药物萃取的传统方法的可行替代方法。