Dispersive solid-phase microextraction method for sample extraction in the analysis of four tetracyclines in water and milk samples by high-performance liquid chromatography with diode-array detection

被引:177
作者
Tsai, Wen-Hsien [2 ]
Huang, Tzou-Chi [2 ]
Huang, Joh-Jong [3 ]
Hsue, Yi-Huu [3 ]
Chuang, Hung-Yi [1 ,4 ]
机构
[1] Kaohsiung Med Univ, Sch Publ Hlth, Kaohsiung 807, Taiwan
[2] Natl Pingtung Univ Sci & Technol, Dept Food Sci, Pingtung 912, Taiwan
[3] Hlth Bur Kaohsiung Cty Govt, Kaohsiung 833, Taiwan
[4] Kaohsiung Med Univ, Dept Community Med, Kaohsiung 807, Taiwan
关键词
Dispersive solid-phase microextraction; Sample preparation; Milk analysis; Water analysis; Tetracyclines; TANDEM MASS-SPECTROMETRY; CHELATE AFFINITY-CHROMATOGRAPHY; PESTICIDE-RESIDUE ANALYSIS; ANIMAL-TISSUES; SORPTIVE EXTRACTION; GAS-CHROMATOGRAPHY; TRACE ANALYSIS; WASTE-WATER; ANTIBIOTICS; SULFONAMIDES;
D O I
10.1016/j.chroma.2009.01.034
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
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. (c) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:2263 / 2269
页数:7
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