Liu Lihong, Yun Zhaojun, He Bin, Jiang Guibin
State Key Laboratory of Environmental Chemistry and Ecotoxicology, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences , P.O. Box 2871, 100085 Beijing, People's Republic of China.
Anal Chem. 2014 Aug 19;86(16):8167-75. doi: 10.1021/ac501347d. Epub 2014 Aug 8.
A simple and highly efficient online system coupling of capillary electrophoresis to inductively coupled plasma-mass spectrometry (CE-ICP-MS) for simultaneous separation and determination of arsenic and selenium compounds was developed. CE was coupled to an ICP-MS system by a sprayer with a novel direct-injection high-efficiency nebulizer (DIHEN) chamber as the interface. By using this interface, six arsenic species, including arsenite (As(III), arsenate (As(V)), monomethylarsonic acid (MMA), dimethylarsinic acid (DMA), arsenobetaine (AsB), and arsenocholine (AsC) and five selenium species (such as sodium selenite (Se(IV)), sodium selenate (Se(VI)), selenocysteine (SeCys), selenomethionine (SeMet), and Se-methylselenocysteine (MeSeCys)) were baseline-separated and determined in a single run within 9 min under the optimized conditions. Minimum dead volume, low and steady sheath flow liquid, high nebulization efficiency, and high sample transport efficiency were obtained by using this interface. Detection limits were in the range of 0.11-0.37 μg L(-1) for the six arsenic compounds (determined as (75)As at m/z 75) and 1.33-2.31 μg L(-1) for the five selenium species (determined as (82)Se at m/z 82). Repeatability expressed as the relative standard deviations (RSD, n = 6) of both migration time and peak area were better than 2.68% for arsenic compounds and 3.28% for selenium compounds, respectively. The proposed method had been successfully applied for the determination of arsenic and selenium species in the certified reference materials DORM-3, water, urine, and fish samples.
开发了一种简单高效的毛细管电泳与电感耦合等离子体质谱联用(CE-ICP-MS)在线系统,用于同时分离和测定砷和硒化合物。通过带有新型直接进样高效雾化器(DIHEN)腔室的喷雾器将CE与ICP-MS系统联用作为接口。利用该接口,在优化条件下,9分钟内可在一次运行中对六种砷化合物(包括亚砷酸盐(As(III))、砷酸盐(As(V))、一甲基胂酸(MMA)、二甲基胂酸(DMA)、砷甜菜碱(AsB)和砷胆碱(AsC))和五种硒化合物(如亚硒酸钠(Se(IV))、硒酸钠(Se(VI))、硒代半胱氨酸(SeCys)、硒代蛋氨酸(SeMet)和硒甲基硒代半胱氨酸(MeSeCys))进行基线分离和测定。使用该接口可实现最小死体积、低且稳定的鞘流液、高雾化效率和高样品传输效率。六种砷化合物(以m/z 75处的(75)As测定)的检测限在0.11 - 0.37 μg L(-1)范围内,五种硒化合物(以m/z 82处的(82)Se测定)的检测限在1.33 - 2.31 μg L(-1)范围内。迁移时间和峰面积的相对标准偏差(RSD,n = 6)表示的重复性,砷化合物分别优于2.68%,硒化合物分别优于3.28%。该方法已成功应用于标准参考物质DORM-3、水、尿液和鱼类样品中砷和硒化合物的测定。