Matoušek Tomáš, Currier Jenna M, Trojánková Nikola, Saunders R Jesse, Ishida María C, González-Horta Carmen, Musil Stanislav, Mester Zoltán, Stýblo Miroslav, Dědina Jiří
Institute of Analytical Chemistry of the ASCR, v. v. i., Veveří 97, 602 00 Brno, Czech Republic.
J Anal At Spectrom. 2013 Sep 1;28(9):1456-1465. doi: 10.1039/C3JA50021G.
An ultra sensitive method for arsenic (As) speciation analysis based on selective hydride generation (HG) with preconcentration by cryotrapping (CT) and inductively coupled plasma- mass spectrometry (ICP-MS) detection is presented. Determination of valence of the As species is performed by selective HG without prereduction (trivalent species only) or with L-cysteine prereduction (sum of tri- and pentavalent species). Methylated species are resolved on the basis of thermal desorption of formed methyl substituted arsines after collection at -196°C. Limits of detection of 3.4, 0.04, 0.14 and 0.10 pg mL (ppt) were achieved for inorganic As, mono-, di- and trimethylated species, respectively, from a 500 μL sample. Speciation analysis of river water (NRC SLRS-4 and SLRS-5) and sea water (NRC CASS-4, CASS-5 and NASS-5) reference materials certified to contain 0.4 to 1.3 ng mL total As was performed. The concentrations of methylated As species in tens of pg mL range obtained by HG-CT-ICP-MS systems in three laboratories were in excellent agreement and compared well with results of HG-CT-atomic absorption spectrometry and anion exchange liquid chromatography- ICP-MS; sums of detected species agreed well with the certified total As content. HG-CT-ICP-MS method was successfully used for analysis of microsamples of exfoliated bladder epithelial cells isolated from human urine. Here, samples of lysates of 25 to 550 thousand cells contained typically tens pg up to ng of iAs species and from single to hundreds pg of methylated species, well within detection power of the presented method. A significant portion of As in the cells was found in the form of the highly toxic trivalent species.
本文介绍了一种基于选择性氢化物发生(HG)、低温捕集(CT)预富集和电感耦合等离子体质谱(ICP-MS)检测的超灵敏砷(As)形态分析方法。通过选择性HG(仅针对三价物种,无需预还原)或L-半胱氨酸预还原(三价和五价物种的总和)来确定As物种的价态。甲基化物种通过在-196°C收集后形成的甲基取代胂的热脱附来分离。对于500μL样品中的无机As、一甲基、二甲基和三甲基化物种,检测限分别达到3.4、0.04、0.14和0.10 pg/mL(ppt)。对经认证总As含量为0.4至1.3 ng/mL的河水(NRC SLRS-4和SLRS-5)和海水(NRC CASS-4、CASS-5和NASS-5)参考物质进行了形态分析。三个实验室的HG-CT-ICP-MS系统获得的数十pg/mL范围内的甲基化As物种浓度高度一致,与HG-CT-原子吸收光谱法和阴离子交换液相色谱-ICP-MS的结果相比也很好;检测到的物种总和与认证的总As含量吻合良好。HG-CT-ICP-MS方法成功用于分析从人尿中分离的脱落膀胱上皮细胞的微量样品。在此,25万至55万个细胞裂解物样品中通常含有数十pg至ng的无机As物种以及单pg至数百pg的甲基化物种,完全在本方法的检测能力范围内。发现细胞中很大一部分As以剧毒的三价物种形式存在。