A rapid method for the determination of methylmercury and inorganic mercury species in whole blood by liquid chromatography with detection using vapor generation ICP-MS/MS†

IF 2.7 3区 化学 Q2 CHEMISTRY, ANALYTICAL Analytical Methods Pub Date : 2025-02-04 DOI:10.1039/D4AY02116A
Emily J. Pacer, Christopher D. Palmer and Patrick J. Parsons
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Abstract

Speciation methods provide a more detailed picture regarding human exposure to toxic metals/metalloids and their effects on human health. The toxicity of methylmercury (MeHg) differs considerably from inorganic mercury (iHg), such that their separation and quantification in whole blood is helpful in identifying sources and possible pathways of exposure. Liquid chromatography (LC) has several advantages over gas chromatography (GC) for the separation of iHg from MeHg due to the former's compatibility with uptake rates of common nebulizer systems used with ICP-MS and the latter's requirement for a derivatization step to produce gaseous Hg species for an effective separation. Here we report an improved method that was developed to separate and quantify MeHg and iHg species in whole blood using isocratic LC elution with determination by vapor generation (VG) coupled with ICP-MS/MS. Chromatographic separation of MeHg and iHg is achieved in ∼4 minutes on a C8 reversed phase column. In those rare cases where there may be human exposure to ethylmercury (EtHg), or where a certified reference material (CRM) is known to contain EtHg (e.g., NIST SRM 955c), all three Hg species can be separated by extending the LC elution time to 8 minutes. Adding VG post column boosts the signal-to-noise ratio, and lowers the LOD. With optimized sample preparation, the LC-VG-ICP-MS/MS method LOD for both iHg and MeHg is 0.2 μg L−1. Method validation was conducted using NIST SRM 955c Toxic Metals in Caprine Blood and NIST SRM 955d Toxic Elements and Metabolites in Frozen Human Blood. Additional validation data were generated using archived blood reference materials from multiple Proficiency Testing programs and External Quality Assessment schemes. Blood-based quality control materials, previously analyzed for Hg species using isotope dilution with GC coupled to ICP-MS, were provided by the US CDC.

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通过分型方法,可以更详细地了解人类接触有毒金属/类金属的情况及其对人体健康的影响。甲基汞(MeHg)的毒性与无机汞(iHg)有很大不同,因此在全血中对其进行分离和定量有助于确定汞的来源和可能的接触途径。在从 MeHg 中分离 iHg 时,液相色谱法(LC)比气相色谱法(GC)更具优势,因为前者与 ICP-MS 使用的普通雾化器系统的吸收率相兼容,而后者需要经过衍生步骤才能产生有效分离的气态汞。在此,我们报告了一种经过改进的方法,该方法采用等度液相色谱洗脱,通过气相发生(VG)和 ICP-MS/MS 联用来分离和定量全血中的甲基汞和碘化汞。在 C8 反相色谱柱上,甲基汞和碘汞的色谱分离只需 4 分钟。在极少数情况下,如果人类可能接触到乙基汞(EtHg),或者已知有证标准物质(CRM)中含有乙基汞(EtHg)(如 NIST SRM 955c),则可以通过将液相色谱洗脱时间延长至 8 分钟来分离所有三种汞。添加 VG 后柱可提高信噪比,降低 LOD。优化样品制备后,LC-VG-ICP-MS/MS 方法的 iHg 和 MeHg 检出限均为 0.2 μg L-1。使用 NIST SRM 955c Caprine 血液中的有毒金属和 NIST SRM 955d 冷冻人体血液中的有毒元素和代谢物进行了方法验证。其他验证数据是使用多个能力验证计划和外部质量评估计划中的存档血液参考材料生成的。美国疾病控制与预防中心(US CDC)提供了基于血液的质量控制材料,这些材料之前曾使用同位素稀释与气相色谱耦合 ICP-MS 分析过汞的种类。
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来源期刊
Analytical Methods
Analytical Methods CHEMISTRY, ANALYTICAL-FOOD SCIENCE & TECHNOLOGY
CiteScore
5.10
自引率
3.20%
发文量
569
审稿时长
1.8 months
期刊介绍: Early applied demonstrations of new analytical methods with clear societal impact
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