Department of Chemistry, National University of Singapore, 3 Science Drive 3, Singapore 117543.
Anal Chem. 2010 Feb 15;82(4):1540-5. doi: 10.1021/ac9023632.
A new two-step microextraction technique, combining dispersive liquid-liquid microextraction (DLLME) and dispersive microsolid-phase extraction (D-micro-SPE), was developed for the fast gas chromatographic-mass spectrometric determination of polycyclic aromatic hydrocarbons (PAHs) in environmental samples. A feature of the new procedure lies in that any organic solvent immiscible with water can be used as extractant in DLLME. A special apparatus, such as conical-bottom test tubes, and tedious procedures of centrifugation, refrigeration of the solvent, and then thawing it, associated with classical DLLME or similar techniques are not necessary in the new procedure, which potentially lends itself to possible automation. In the present D-micro-SPE approach, hydrophobic magnetic nanoparticles were used to retrieve the extractant of 1-octanol in the DLLME step. It is noteworthy that the target of D-micro-SPE was the 1-octanol rather than the PAHs. Because of the rapid mass transfer associated with the DLLME and the D-micro-SPE steps, fast extraction could be achieved. Parameters affecting the extraction efficiency were investigated in detail. The optimal conditions were as follows: vortex at 3200 rpm in the DLLME step for 2 min and in D-micro-SPE for 1 min and then desorption by sonication for 4 min with acetonitrile as the solvent. The results demonstrated that enrichment factors ranging from 110- to 186-fold were obtained for the analytes. The limits of detection and the limits of quantification were in the range of 11.7-61.4 pg/mL and 0.04-0.21 ng/mL, respectively. The linearities were 0.5-50, 1-50, or 2-50 ng/mL for different PAHs. Finally, the two-step extraction method was successfully used for the fast determination of PAHs in river water samples. This two-step method, combining two different and efficient miniaturized techniques, provides a fast means of sample pretreatment for environmental water samples.
一种新的两步微萃取技术,结合分散液液微萃取(DLLME)和分散微固相萃取(D-micro-SPE),被开发用于快速气相色谱-质谱法测定环境样品中的多环芳烃(PAHs)。新方法的一个特点在于,任何与水不混溶的有机溶剂都可以用作 DLLME 中的萃取剂。在新方法中,不需要特殊的仪器,如锥形底试管,也不需要离心、溶剂冷藏和解冻等繁琐的步骤,这使其有可能实现自动化。在本研究的 D-micro-SPE 方法中,使用疏水性磁性纳米粒子回收 DLLME 步骤中 1-辛醇的萃取剂。值得注意的是,D-micro-SPE 的目标是 1-辛醇而不是 PAHs。由于 DLLME 和 D-micro-SPE 步骤中快速的质量传递,实现了快速萃取。详细研究了影响萃取效率的参数。优化条件为:在 DLLME 步骤中以 3200 rpm 涡旋 2 分钟,在 D-micro-SPE 中涡旋 1 分钟,然后用乙腈超声洗脱 4 分钟。结果表明,分析物的富集因子范围为 110-186 倍。检测限和定量限分别为 11.7-61.4 pg/mL 和 0.04-0.21 ng/mL。不同 PAHs 的线性范围为 0.5-50、1-50 或 2-50 ng/mL。最后,该两步萃取方法成功用于快速测定河水样品中的 PAHs。这种两步法结合了两种不同且高效的微型技术,为环境水样提供了快速的样品预处理方法。