Mercury speciation in whole blood by gas chromatography coupled to ICP-MS with a fast microwave-assisted sample preparation procedure

被引:38
|
作者
Rodrigues, Jairo L. [2 ]
Alvarez, Carolina Rodriguez [1 ]
Farinas, Nuria Rodriguez [1 ]
Berzas Nevado, Juan J. [3 ]
Barbosa, Fernando, Jr. [4 ]
Rodriguez Martin-Doimeadios, Rosa C. [1 ]
机构
[1] Univ Castilla La Mancha, Fac Ciencias Med Ambiente, Toledo 45071, Spain
[2] Univ Fed Vales Jequitinhonha & Mucuri, Inst Ciencia & Tecnol Mucuri, Teofilo Otoni, MG, Brazil
[3] Univ Castilla La Mancha, Fac Ciencias Quim, E-13071 Ciudad Real, Spain
[4] Univ Sao Paulo, Fac Ciencias Farmaceut Ribeirao Preto, Lab Toxicol & Essencialidade Metais, BR-05508 Sao Paulo, Brazil
关键词
PLASMA-MASS SPECTROMETRY; ATOMIC-ABSORPTION-SPECTROMETRY; TETRAMETHYLAMMONIUM HYDROXIDE SOLUBILIZATION; ROOM-TEMPERATURE; HUMAN HAIR; SODIUM TETRA(N-PROPYL)BORATE; FLUORESCENCE DETECTION; BIOLOGICAL TISSUES; ALKALINE DIGESTION; METHYL MERCURY;
D O I
10.1039/c004931j
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A simple and fast method is described for simultaneous determination of methylmercury (MeHg), ethylmercury (Et-Hg) and inorganic mercury (Ino-Hg) in blood samples by using capillary gas chromatography-inductively coupled plasma mass spectrometry (GC-ICP-MS) after derivatization and alkaline digestion. Closed-vessel microwave assisted digestion conditions with tetramethylammonium hydroxide (TMAH) have been optimized. Derivatization by using ethylation and propylation procedures have also been evaluated and compared. The absolute detection limits (using a 1 mu L injection) obtained by GC-ICP-MS with ethylation were 40 fg for MeHg and Ino-Hg, respectively, and with propylation were 50, 20 and 50 fg for MeHg, Et-Hg and Ino-Hg, respectively. Method accuracy is traceable to Standard Reference Material (SRM) 966 Toxic Metals in Bovine Blood from the National Institute of Standards and Technology (NIST). Additional validation is provided based on the comparison of results obtained for mercury speciation in blood samples with the proposed procedure and with a previously reported LC-ICP-MS method. With the new proposed procedure no tedious clean-up steps are required and a considerable improvement of the time of analysis was achieved compared to other methods using GC separation.
引用
收藏
页码:436 / 442
页数:7
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