State Key Laboratory of Marine Environmental Science, Environmental Science Research Center, Xiamen University, 361005 Xiamen, China.
Talanta. 2011 Sep 30;85(4):2212-7. doi: 10.1016/j.talanta.2011.07.066. Epub 2011 Jul 27.
The commercial solid phase microextraction (SPME) fibers are not stable enough in organic solvent and tend to swell and strip off from the silica fiber in the high performance liquid chromatography (HPLC) mobile phase, and therefore the application of SPME coupled online with HPLC is limited. In this study, an SPME fiber coated with single walled carbon nanotubes (SWCNTs), prepared by means of electrophoretic deposition, was coupled on line to HPLC for the determination of four endocrine-disrupting compounds, i.e. bisphenol A (BPA), estrone (E(1)), 17α-ethynylestradiol (EE(2)) and octylphenol (OP), in aqueous samples. The results showed that the SWCNTs coating on the prepared fiber did not swell and strip off from the platinum fiber throughout the experiment, thus indicating a high resistance to the HPLC mobile phase, the mixture of water and acetonitrile. The SWCNTs fiber had similar (for OP) or higher (for BPA, EE(2) and E(1)) extraction efficiencies than the commonly used polyacrylate fiber, and had a lifetime of more than 120 operation times. Under the optimized conditions, the linearity of the proposed method was 1.0-30.0 μg/L for BPA and OP and 3.0-90.0 μg/L for E(1) and EE(2). The limits of detection (LODs; S/N=3) and limits of quantification (LOQs; S/N=10) of the method were 0.32-0.52 μg/L and 1.06-1.72 μg/L, respectively. Repeatability for one fiber (n=3) was in the range of 1.3-7.1% and fiber-to-fiber reproducibility (n=3) was in the range of 1.6-8.4%. The proposed method was successfully applied for the analysis of spiked tap water and seawater samples with recoveries from 81.8 to 97.3%.
商业固相微萃取(SPME)纤维在有机溶剂中不够稳定,在高效液相色谱(HPLC)流动相中容易膨胀和从二氧化硅纤维上剥落,因此 SPME 与 HPLC 的在线联用受到限制。在本研究中,通过电泳沉积制备的单壁碳纳米管(SWCNTs)涂覆的 SPME 纤维与 HPLC 在线联用,用于测定四种内分泌干扰化合物,即双酚 A(BPA)、雌酮(E(1))、17α-乙炔基雌二醇(EE(2))和辛基酚(OP),在水样中。结果表明,在整个实验过程中,制备的纤维上的 SWCNTs 涂层没有从铂纤维上膨胀和剥落,因此对 HPLC 流动相(水和乙腈的混合物)具有高抗性。SWCNTs 纤维的萃取效率与常用的聚丙烯酸纤维相似(对于 OP)或更高(对于 BPA、EE(2)和 E(1)),且使用寿命超过 120 次操作。在优化条件下,该方法对 BPA 和 OP 的线性范围为 1.0-30.0 μg/L,对 E(1)和 EE(2)的线性范围为 3.0-90.0 μg/L。该方法的检出限(LOD;S/N=3)和定量限(LOQ;S/N=10)分别为 0.32-0.52 μg/L 和 1.06-1.72 μg/L。一根纤维(n=3)的重复性在 1.3-7.1%范围内,三根纤维(n=3)的纤维间重现性在 1.6-8.4%范围内。该方法成功应用于加标自来水和海水样品的分析,回收率为 81.8-97.3%。