Tsai Wen-Hsien, Huang Tzou-Chi, Huang Joh-Jong, Hsue Yi-Huu, Chuang Hung-Yi
Department of Food Science, National Pingtung University of Science and Technology, Pingtung, Taiwan.
J Chromatogr A. 2009 Mar 20;1216(12):2263-9. doi: 10.1016/j.chroma.2009.01.034. Epub 2009 Jan 17.
A dispersive solid-phase microextraction (dispersive-SPME) method for the determination of tetracycline, oxytetracycline, chlortetracycline and doxycycline is proposed. Different silica-based and polymeric sorbents were evaluated for their capacity to simultaneously preconcentrate tetracyclines (TCs) in the dispersive format from aqueous or organic solutions. Silica-based sorbents especially functionalized with primary amine, secondary amine, or carbonyl groups have showed higher capacity than polymeric sorbents under organic environment. In the proposed dispersive solid-phase microextraction method, after extraction with acetonitrile and salt-promoted partitioning, TCs were adsorbed to a small amount of dispersive silica-based primary and secondary amine sorbents, desorbed with a small volume of desorption solution, and determined by high-performance liquid chromatography with diode-array detection. Under the optimal conditions, recoveries were determined for surface water and milk samples spiked at 10 ng/mL and 50-150 ng/g, respectively, and quantification was achieved by matrix-matched calibration. The calibration curves of four TCs in both samples showed linearity with a correlation coefficient value above 0.997. Average recoveries ranged from 97.1 to 104.1% and the precision was from 2.0 to 5.6%. Limits of detection ranged from 0.7 to 3.5 ng/mL and from 7.9 to 35.3 ng/g for four TCs surface in surface water and milk samples, respectively.
本文提出了一种用于测定四环素、土霉素、金霉素和强力霉素的分散固相微萃取(dispersive-SPME)方法。评估了不同的硅胶基和聚合物吸附剂从水相或有机溶液中以分散形式同时预富集四环素类(TCs)的能力。在有机环境下,特别是用伯胺、仲胺或羰基官能化的硅胶基吸附剂比聚合物吸附剂表现出更高的富集能力。在所提出的分散固相微萃取方法中,用乙腈萃取并经盐促进分配后,TCs被吸附到少量分散的硅胶基伯胺和仲胺吸附剂上,用少量解吸溶液解吸,然后通过配有二极管阵列检测器的高效液相色谱法进行测定。在最佳条件下,分别对加标浓度为10 ng/mL的地表水样品和加标浓度为50 - 150 ng/g的牛奶样品进行回收率测定,并通过基质匹配校准实现定量分析。两个样品中四种TCs的校准曲线均呈线性,相关系数值高于0.997。平均回收率在97.1%至104.1%之间,精密度在2.0%至5.6%之间。地表水和牛奶样品中四种TCs的检测限分别为0.7至3.5 ng/mL和7.9至35.3 ng/g。