Biomonitoring for arsenic, toxic and essential metals in single hair strands by laser ablation inductively coupled plasma mass spectrometry

被引:20
作者
Kumtabtim, Usarat [1 ,2 ,3 ]
Matusch, Andreas [4 ]
Dani, Sergio Ulhoa [5 ]
Siripinyanond, Atitaya [2 ,3 ]
Becker, J. Sabine [1 ]
机构
[1] Forschungszentrum Julich, BrainMet Lab, Cent Div Analyt Chem, D-52425 Julich, Germany
[2] Mahidol Univ, Fac Sci, Dept Chem, Bangkok 10400, Thailand
[3] Mahidol Univ, Fac Sci, Ctr Innovat Chem, Bangkok 10400, Thailand
[4] Forschungszentrum Julich, Inst Neurosci & Med INM 2, D-52425 Julich, Germany
[5] Univ Heidelberg Hosp, Dept Internal Med, D-69120 Heidelberg, Germany
关键词
Arsenic; Biomonitoring; Hair strand; Laser ablation inductively coupled plasma mass spectrometry; Metal distribution; LA-ICP-MS; MICROWAVE DIGESTION; ELEMENTS; INDIVIDUALS; POPULATION; METABOLISM; EXPOSURE; ANTIMONY; PROVINCE; MERCURY;
D O I
10.1016/j.ijms.2011.03.007
中图分类号
O64 [物理化学(理论化学)、化学物理学]; O56 [分子物理学、原子物理学];
学科分类号
070203 ; 070304 ; 081704 ; 1406 ;
摘要
Laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS) has been developed as reliable analytical technique for the quantitation of metal distributions at micrometre resolution. In this work a novel microanalytical strategy for biomonitoring of arsenic, toxic and essential metals in single hair strands is proposed. Two different calibration strategies in LA-ICP-MS were developed using either certified hair standard reference material (IAEA 086) or prepared matrix-matched laboratory hair standards doped with analytes of interest at defined concentration. Powdered hair standards and human hair strands mounted on a sticky tape in the LA chamber were analyzed under the same experimental conditions by an optimized LA-ICP-MS technique. The use of hair powder standard allows calibration curves to be obtained by plotting the analyte ion (M(+)) intensity normalized to (34)S(+) (the ratio M(+)/(34)S(+)) as a function of the concentration determined by ICP-MS of acidic digests. The linear correlation coefficients (R) of calibration curves for analytes As, Ba, Cd, Ce, Co, Cr, Cu, Fe, Ga, Hg, Mg, Mo, Ni, Pb, Rb, Sr, Ti and U were typically between 0.985 and 0.999. The limit of detection (LOD) was 0.6 mu g g(-1) for As and ranged from 0.3 to 7.8 mu g g(-1) for the other analytes. Distinct elemental exposition time profiles were observed in hair samples from five volunteers. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:185 / 191
页数:7
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