Roldán-Pijuán Mercedes, Lucena Rafael, Cárdenas Soledad, Valcárcel Miguel, Kabir Abuzar, Furton Kenneth G
Department of Analytical Chemistry, Institute of Fine Chemistry and Nanochemistry, Marie Curie Building, Campus de Rabanales, University of Córdoba, 14071 Córdoba, Spain.
Department of Analytical Chemistry, Institute of Fine Chemistry and Nanochemistry, Marie Curie Building, Campus de Rabanales, University of Córdoba, 14071 Córdoba, Spain.
J Chromatogr A. 2015 Jan 9;1376:35-45. doi: 10.1016/j.chroma.2014.12.027. Epub 2014 Dec 12.
Stir fabric phase sorptive extraction (SFPSE), which integrates sol-gel hybrid organic-inorganic coated fabric phase sorptive extraction media with a magnetic stirring mechanism, is presented for the first time. Two flexible fabric substrates, cellulose and polyester were used as the host matrix for three different sorbents e.g., sol-gel poly(tetrahydrofuran), sol-gel poly(ethylene glycol), and sol-gel poly(dimethyldiphenylsiloxane). The new microextraction device has been analytically evaluated using triazine herbicides as model compounds. The factors affecting the extraction efficiency of SFPSE have been investigated and the optimal extraction conditions have been determined. Under these optimum conditions, the limits of quantification (LOQs) for sol-gel poly(ethylene glycol) coated SFPSE device in combination with UPLC-DAD for the analysis of the seven triazine herbicides were in the range of 0. 26-1.50μg/L with precision (relative standard deviation) at 2μg/L concentration ranging from 1.4-4.8% (intra-day, n=5) and 6.8-11.8% (inter-day, n=3). Enrichment factors were found between 444 and 1411 (compared to 2000 theoretical maximum). Absolute extraction recoveries were in the range of 22.2-70.5%. The developed method was applied for the determination of selected triazine herbicides from three river water samples. Relative recoveries of the target analytes, in the range from 75 to 126%, were found to be satisfactory. The combination of SFPSE with LC-MS/MS allows the improvement of the method sensitivity to the range from 0.015μg/L to 0.026μg/L with precision better than 10.8% expressed as relative standard deviation (RSD).
首次提出了搅拌织物相吸附萃取(SFPSE)方法,该方法将溶胶-凝胶杂化有机-无机涂层织物相吸附萃取介质与磁力搅拌机制相结合。使用两种柔性织物基材,即纤维素和聚酯,作为三种不同吸附剂的主体基质,例如溶胶-凝胶聚四氢呋喃、溶胶-凝胶聚乙二醇和溶胶-凝胶聚二甲基二苯基硅氧烷。以三嗪类除草剂为模型化合物,对新型微萃取装置进行了分析评估。研究了影响SFPSE萃取效率的因素,并确定了最佳萃取条件。在这些最佳条件下,溶胶-凝胶聚乙二醇涂层SFPSE装置与超高效液相色谱-二极管阵列检测器(UPLC-DAD)联用分析七种三嗪类除草剂时的定量限(LOQ)在0.26-1.50μg/L范围内,在2μg/L浓度下的精密度(相对标准偏差),日内为1.4-4.8%(n=5),日间为6.8-11.8%(n=3)。富集因子在444至1411之间(与理论最大值2000相比)。绝对萃取回收率在22.2-70.5%范围内。所建立的方法用于测定三个河水样品中选定的三嗪类除草剂。目标分析物的相对回收率在75%至126%之间,结果令人满意。SFPSE与液相色谱-串联质谱(LC-MS/MS)联用可将方法灵敏度提高到0.015μg/L至0.026μg/L范围,精密度优于10.8%,以相对标准偏差(RSD)表示。