College of Life Sciences, Jilin University, Changchun, 130012, China.
College of Chemistry, Jilin University, Changchun, 130012, China.
Environ Sci Pollut Res Int. 2018 Jun;25(16):16121-16134. doi: 10.1007/s11356-018-1581-6. Epub 2018 Mar 29.
In this work, a fast and selective method based on magnetic extraction is presented for the simultaneous extraction of sulfonamides (SAs) and fluoroquinolones (FQs), followed by liquid chromatography-tandem mass spectrometry detection. In this method, magnetic surface double-template molecularly imprinted polymers (MSdt-MIPs) with superparamagnetic property and high selectivity toward both SAs and FQs were synthesized and directly applied to the simultaneous extraction of SAs and FQs from environmental water as magnetic adsorbents. The extraction and enrichment procedures could be accomplished in one single step by stirring the mixture of MSdt-MIPs and water sample, and the MSdt-MIPs with adsorbed analytes were easily separated from the water sample by a magnet afterwards. The adsorption mechanism of MSdt-MIPs was investigated by employing the adsorption thermodynamic and kinetic studies, and the selectivity of the MSdt-MIPs toward target analytes was evaluated through the selectivity test. For validation of the proposed method, the matrix effect was evaluated and compared to that of the traditional SPE method. Excellent linearity (R > 0.9990) for both SAs and FQs were obtained in the concentration range of 20-2000 ng L, and the limits of detection are in the range of 3.0-4.7 ng L for SAs while 4.1-6.1 ng L for FQs. Finally, the proposed method was successfully applied to the simultaneous determination of SAs and FQs in several environmental water samples.
在这项工作中,提出了一种基于磁萃取的快速选择性方法,用于同时提取磺胺类(SAs)和氟喹诺酮类(FQs),并进行液相色谱-串联质谱检测。在该方法中,合成了具有超顺磁性和对 SAs 和 FQs 均具有高选择性的磁性表面双模板分子印迹聚合物(MSdt-MIPs),并将其直接用作从环境水样中同时提取 SAs 和 FQs 的磁性吸附剂。通过搅拌 MSdt-MIPs 和水样的混合物,可以在一步中完成萃取和富集过程,然后用磁铁将吸附有分析物的 MSdt-MIPs 从水样中轻易分离。通过吸附热力学和动力学研究,研究了 MSdt-MIPs 的吸附机制,并通过选择性测试评估了 MSdt-MIPs 对目标分析物的选择性。为了验证所提出的方法,评估了基质效应并与传统 SPE 方法进行了比较。对于 SAs 和 FQs,在 20-2000ng L 的浓度范围内均获得了极好的线性(R>0.9990),磺胺类的检测限范围为 3.0-4.7ng L,而氟喹诺酮类的检测限范围为 4.1-6.1ng L。最后,该方法成功应用于几种环境水样中 SAs 和 FQs 的同时测定。