A novel method of ultrasound-assisted dispersive liquid-liquid microextraction coupled to liquid chromatography-mass spectrometry for the determination of trace organoarsenic compounds in edible oil

被引:60
作者
Wang, Wei-Xun [1 ]
Yang, Tzung-Jie [1 ]
Li, Zu-Guang [1 ,2 ]
Jong, Ting-Ting [1 ]
Lee, Maw-Rong [1 ]
机构
[1] Natl Chung Hsing Univ, Dept Chem, Taichung 402, Taiwan
[2] Zhejiang Univ Technol, Coll Chem Engn & Mat Sci, Hangzhou 310014, Zhejiang, Peoples R China
关键词
Ultrasound-assisted dispersive liquid-liquid microextraction; Organoarsenicals; Edible oil; Liquid chromatography-mass spectrometry; ATOMIC-ABSORPTION-SPECTROMETRY; SOLID-PHASE MICROEXTRACTION; MANUFACTURED SEAFOOD PRODUCTS; ELECTRON-CAPTURE DETECTION; HPLC-ICP-MS; GAS-CHROMATOGRAPHY; WATER SAMPLES; HYDRIDE GENERATION; EMISSION-SPECTROMETRY; ARSENIC SPECIATION;
D O I
10.1016/j.aca.2011.02.033
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A novel approach, ultrasound-assisted dispersive liquid-liquid microextraction combined with liquid chromatography-mass spectrometry (UA-DLLME with LC-MS) is demonstrated to be quite useful for the determination of trace amounts of organoarsenic compounds in edible oil. The organoarsenic compounds studied include dimethylarsinic acid (DMA), monomethylarsonic acid (MMA) and 3-nitro-4-hydroxyphenyl arsenic acid (Roxarsone). Orthogonal array experimental design (OAD) was utilized to investigate the parameter space of conditions for UA-DLLME. The optimum conditions were found to be 4 min of ultrasonic extraction using 1.25 mL of mixed solvent with 50 mu L of buffer solution. Under these optimal conditions, the linear range was from 10 ng g(-1) tc 500 ng g(-1) for DMA and Roxarsone, from 25 ng g(-1) to 500 ng g(-1) for MMA. Limits of detection of DMA, MMA and Roxarsone were 1.0 ng g(-1), 3.0 ng g(-1) and 5.8 ng g(-1), respectively. The precisions and recoveries also were investigated by spiking 3-level concentrations in edible oil. The recoveries obtained were over 89.9% with relative standard deviation (RSD) of 9.6%. The new approach was utilized to successfully detect trace amounts of organoarsenic compounds in various edible oil samples. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:221 / 227
页数:7
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