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首页> 外文期刊>Journal of Analytical Atomic Spectrometry >Mercury speciation in whole blood by gas chromatography coupled to ICP-MS with a fast microwave-assisted sample preparation procedure
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Mercury speciation in whole blood by gas chromatography coupled to ICP-MS with a fast microwave-assisted sample preparation procedure

机译:气相色谱-ICP-MS联用快速微波辅助样品制备方法测定全血中的汞形态

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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 μL 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.
机译:介绍了一种使用毛细管气相色谱-电感耦合等离子体质谱法(GC-ICP-MS)同时测定血液样品中甲基汞(MeHg),乙基汞(Et-Hg)和无机汞(Ino-Hg)的简单快速的方法)衍生化和碱消化后。已优化了使用氢氧化四甲铵(TMAH)的密闭容器微波辅助消化条件。还已经评估并比较了通过使用乙基化和丙基化程序进行的衍生化。进行乙基化的GC-ICP-MS获得的绝对检出限(使用1μL进样)对于MeHg和Ino-Hg分别为40 fg,对于MeHg,Et-Hg和Ino丙基化分别为50、20和50 fg -汞,分别。方法的准确性可追溯到美国国家标准技术研究院(NIST)的标准参考物质(SRM)966牛血中的有毒金属。基于对血液样品中汞形态分析结果与拟议程序以及先前报道的LC-ICP-MS方法的比较,提供了进一步的验证。与使用GC分离的其他方法相比,采用新提出的方法无需繁琐的清理步骤,并且大大缩短了分析时间。

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  • 来源
    《Journal of Analytical Atomic Spectrometry》 |2011年第2期|p.436-442|共7页
  • 作者单位

    Instituto de Ciencia e Tecnologia do Mucuri, Universidade Federal dos Vales do Jequitinhonha e Mucuri, Tedfilo Otoni, MG, Brasil;

    Facultad de Ciencias del Medio Ambiente, Universidad de Castilla-La Mancha, 45071 Toledo, Espana;

    Facultad de Ciencias del Medio Ambiente, Universidad de Castilla-La Mancha, 45071 Toledo, Espana;

    Facultad de Ciencias Quimicas, Universidad de Castilla-La Mancha,13071 Ciudad Real, Espaha;

    Laborat6rio de Toxicologia e Essencialidade de Metais, Faculdade de Ciencias Farmaceuticas de Ribeirao Preto, Universidade de Sao Paulo, Brasil;

    Facultad de Ciencias del Medio Ambiente, Universidad de Castilla-La Mancha, 45071 Toledo, Espana;

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