Identification and quantitation of diethylstilbestrol in aquatic products using gas chromatography coupled with triple quadrupole tandem mass spectrometry

被引:10
作者
Ke, Chang-liang [1 ,2 ]
Wang, Zeng-huan [1 ,2 ]
Gan, Ju-li [1 ,2 ]
Gu, Yang-guang [1 ,3 ]
Huang, Ke [1 ,2 ]
Li, Liu-dong [1 ,2 ]
Lin, Qin [1 ,3 ]
机构
[1] Chinese Acad Fishery Sci, South China Sea Fisheries Res Inst, Guangzhou 510300, Guangdong, Peoples R China
[2] Minist Agr, Key Lab Aquat Prod Proc, Guangzhou 510300, Guangdong, Peoples R China
[3] Key Lab Fishery Ecol & Environm, Guangzhou 510300, Guangdong, Peoples R China
来源
RSC ADVANCES | 2014年 / 4卷 / 05期
关键词
PERFORMANCE LIQUID-CHROMATOGRAPHY; LINKED-IMMUNOSORBENT-ASSAY; SOLID-PHASE EXTRACTION; (ULTRA)TRACE ANALYSIS; TRACE ANALYSIS; SURFACE-WATER; WASTE-WATER; LC-MS/MS; ESTROGENS; RESIDUES;
D O I
10.1039/c3ra44676j
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We developed a highly sensitive and specific method for determining DES residue in fish meat using gas chromatography coupled with tandem mass spectrometry (GC-MS-MS) with a triple quadrupole analyzer (QqQ). The samples were extracted using ethyl acetate, cleaned using florisil, and derivatized using a mixture of 99% N, O-bis(trimethylsilyl) trifluoroacetamide (BSTFA) and 1% trimethylchlorosilane (TMCS). The results showed that the GC-MS-MS system presented great advantages for the identification and quantitation of DES in fish meat. The limit of detection (LOD) and limit of quantification (LOQ) values were 0.0142 mu g kg(-1) and 0.0475 mu g kg(-1), respectively. The recoveries from the spiked fish samples spiked at four levels were in the range of 86.1% to 106%. The precision of the method was evaluated using the relative standard deviation (RSD) and ranged from 1.39% to 9.62%. The linear range was from 1.00 to 100 mu g L-1 with good linearity (r = 0.9998). It can be concluded that the method is reliable for identifying and detecting DES residue at trace levels in aquatic products.
引用
收藏
页码:2355 / 2359
页数:5
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