Es'haghi Z
Department of Chemistry, Faculty of Sciences, Payame Noor University, Iran. zarrin
Anal Chim Acta. 2009 May 8;641(1-2):83-8. doi: 10.1016/j.aca.2009.03.043. Epub 2009 Apr 2.
The aim of this study was to develop an analytical procedure which allows the quantification of pharmaceuticals in water at the ng L(-1) level. Hence, it is reported research on the application of a rapid, inexpensive and simple continuous hollow fiber liquid-phase micro extraction (CHF-LPME) for the pre-concentration and determination of non-steroidal anti-inflammatory drugs (NSAIDs), such as ibuprofen (IBP), naproxen (NAP), and ketoprofen (KEP), in wastewater. In this method, a 2.50 cm end sealed piece of a polypropylene hollow fiber was immersed into the organic solvent, octanol, for 30 s. After solvent impregnation with the pores of the fiber, the excess amounts of solvent were removed from inside the fiber, and 4.0 microL of octanol, as the acceptor phase, was injected into the fiber carefully. The fiber was settled using a microsyringe into a 10.0 mL glass test tube, and 20.00 mL of the aqueous solution (the donor phase), was circulated by a pump around it. After analyte extraction for an optimized period of time (20 min), 2 microL of the organic solvent was withdrawn into the microsyringe and injected into the GC-FID for further analysis. Finally, based on the optimized analytical conditions, the method was linear in the range of 2.5-500 ng L(-1). The limits of detection were 1-2 ng L(-1). Repeatability of this method on an intra-day scale was 3.4-10.2% (RSD%). NSAIDs have been detected in several municipal wastewater samples, and the concentration range was 9.0-19.0 ng L(-1).
本研究的目的是开发一种分析程序,能够对水中纳克每升(ng L⁻¹)水平的药物进行定量分析。因此,本文报道了一种快速、廉价且简单的连续中空纤维液相微萃取(CHF-LPME)方法在废水样品中对非甾体抗炎药(NSAIDs)如布洛芬(IBP)、萘普生(NAP)和酮洛芬(KEP)进行预浓缩和测定的应用研究。在该方法中,将一段2.50厘米长、一端密封的聚丙烯中空纤维浸入有机溶剂正辛醇中30秒。待纤维孔隙被溶剂浸渍后,将纤维内部多余的溶剂去除,然后小心地向纤维内注入4.0微升正辛醇作为接受相。使用微量注射器将纤维放入一个10.0毫升的玻璃试管中,通过泵使20.00毫升水溶液(供体相)在其周围循环。在经过优化的萃取时间(20分钟)对分析物进行萃取后,将2微升有机溶剂吸入微量注射器并注入气相色谱 - 火焰离子化检测器(GC-FID)进行进一步分析。最后,基于优化后的分析条件,该方法在2.5 - 500 ng L⁻¹范围内呈线性。检测限为1 - 2 ng L⁻¹。该方法日内的重复性相对标准偏差(RSD%)为3.4 - 10.2%。在多个城市废水样品中检测到了NSAIDs,其浓度范围为9.0 - 19.0 ng L⁻¹。