College of Chemistry and Chemical Engineering, Northwest Normal University, PR China; Key Laboratory of Bioelectrochemistry & Environmental Analysis of Gansu Province, Lanzhou 730070, PR China.
College of Chemistry and Chemical Engineering, Northwest Normal University, PR China.
Talanta. 2019 Mar 1;194:7-13. doi: 10.1016/j.talanta.2018.10.027. Epub 2018 Oct 12.
A novel Estrone (E1) molecularly imprinted polymers (MIPs-E1)-coated solid-phase microextraction (SPME) fiber was prepared by in-situ polymerization on inner and outer surface of the capillary, namely MIPs-E1-coated in-out-tube SPME (MIPs-E1-IOT-SPME), which combines the advantages of enhanced extraction efficiencies of IOT-SPME and specific adsorption abilities of MIPs, and shows nearly double enrichment capacity compared to in-tube SPME (IT-SPME). The extraction conditions were optimized and a method for determination six endocrine disrupting compounds (EDCs) by MIPs-E1-IOT-SPME coupled with HPLC is developed. The MIPs-E1 coating was characterized by fourier-transform infrared spectrometry (FTIR), scanning electron microscopy (SEM), N adsorption-desorption and Thermal gravimetric analysis (TGA). Under the optimum condition, the MIPs-IOT-SPME-HPLC method shows low limits of detection (LODs) (0.21-0.80 μg L) and limits of quantification detection (LOQs) (0.69-2.6 μg L), wide linear ranges from 10.0 to 1000 μg L for each compound with exception of E2 and E3 from 20.0 to 1000 μg L, and acceptable reproducibility of one fiber for five parallel determinations is 2.4-6.6% (RSD) and fiber-to-fiber is 4.5-8.1% (RSD). The satisfactory recoveries are in the range of 88.5-105.1% with good RSDs less than 7.9% at the five spiked levels of 20.0, 50.0, 80.0, 200.0 and 500.0 μg L. Moreover, when compared with commercial fibers, the MIPs-E1-IOT-SPME fiber displays excellent adsorption capacity and specific selectivity.
一种新型 Estrone(E1)分子印迹聚合物(MIPs-E1)-涂层固相微萃取(SPME)纤维是通过在毛细管内外表面原位聚合制备的,即 MIPs-E1-内外管 SPME(MIPs-E1-IOT-SPME),它结合了 IOT-SPME 增强的萃取效率和 MIPs 的特异性吸附能力的优点,与内管 SPME(IT-SPME)相比,其富集容量几乎增加了一倍。优化了萃取条件,并建立了 MIPs-E1-IOT-SPME 结合 HPLC 测定六种内分泌干扰化合物(EDCs)的方法。通过傅里叶变换红外光谱(FTIR)、扫描电子显微镜(SEM)、N 吸附-解吸和热重分析(TGA)对 MIPs-E1 涂层进行了表征。在最佳条件下,MIPs-IOT-SPME-HPLC 方法的检测限(LOD)(0.21-0.80μg/L)和定量检测限(LOQ)(0.69-2.6μg/L)较低,每个化合物的线性范围从 10.0 到 1000μg/L,除了 E2 和 E3 从 20.0 到 1000μg/L,对于每个化合物的线性范围都很宽,每个化合物的五个平行测定的重复性好,纤维间的重复性为 2.4-6.6%(RSD),纤维间的重复性为 4.5-8.1%(RSD)。在 20.0、50.0、80.0、200.0 和 500.0μg/L 的五个加标水平下,回收率在 88.5-105.1%范围内,RSD 小于 7.9%。此外,与商业纤维相比,MIPs-E1-IOT-SPME 纤维表现出优异的吸附能力和特异性选择性。