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On the certification of cadmium at trace and ultratrace levels in standard reference materials using ID ICP-MS

机译:关于使用ID ICP-MS对标准参考物质中痕量和超痕量镉的认证

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Analytical methods used for the isotope dilution inductively coupled plasma mass spectrometric (ID-ICP-MS) measurement of Cd at μg kg?1 and sub-μg kg?1 levels are described and applied to the certification of new dietary supplement, blood, and serum Standard Reference Materials (SRMs). The materials are: SRM 3240 Ephedra sinica Stapf Aerial Parts, SRM 3241 Ephedra sinica Stapf Native Extract, SRM 3243 Ephedra-Containing Solid Oral Dosage Form, SRM 3244 Ephedra-Containing Protein Powder, SRM 966 Toxic Metals in Bovine Blood, Level 1 (L1) and Level 2 (L2), and SRM 1598a Animal Serum. The concentration of Cd in the materials ranges from 120 μg kg?1 down to 0.03 μg kg?1. At these levels, the factors that most influence the accuracy of the ICP-MS data are the procedure blank and spectral and nonspectral interferences. Nonspectral interference, caused by the high concentration of dissolved solids in the matrices investigated, resulted in signal suppression. Matrix separation was used to enhance signal intensity and to reduce spectral interference for the accurate determination of Cd in SRM 1598a and SRM 3244. Chromatographic separation procedures using Chelex for SRM 1598a and anion exchange for SRM 3244 were optimized to achieve the desired separation characteristics without substantially increasing the procedure blank. Sensitivity for the determination of Cd in serum was additionally enhanced through the use of desolvation nebulization. We determined that separations were not required for the accurate ICP-MS determination of Cd in SRM 3240, SRM 3241, SRM 3243, and SRM 966 L2 under optimized analysis conditions. These samples were diluted to a minimum volume and introduced to the ICP-MS via low flow (40–100 μL/min) microconcentric nebulizers. SRM 966 L1 was also analyzed directly, but results were highly variable. The ID-ICP-MS sample preparation and ratio measurement protocols described here resulted in total expanded uncertainties of less than 1% for the determination of 90.85 μg kg?1 Cd in SRM 3240, and less than 10% total expanded uncertainty for the determination of 0.0468 μg kg?1 Cd in SRM 1598a.
机译:描述了用于同位素稀释电感耦合等离子体质谱法(ID-ICP-MS)的Cd在μgkg?1 和亚μgkg?1 水平的分析方法,并将其应用于认证新的膳食补充剂,血液和血清标准参考物质(SRM)。这些材料是:SRM 3240麻黄制片空中零件,SRM 3241麻黄制片天然提取物,SRM 3243麻黄制固体口服剂型,SRM 3244麻黄制蛋白粉,SRM 966牛血中的有毒金属1级(L1) )和2级(L2),以及SRM 1598a动物血清。材料中Cd的浓度范围从120μgkg?1 到0.03μgkg?1 。在这些级别上,最影响ICP-MS数据准确性的因素是程序空白以及光谱和非光谱干扰。由所研究的基质中高浓度的溶解固体引起的非光谱干扰导致信号抑制。为了准确测定SRM 1598a和SRM 3244中的Cd,使用了基质分离来增强信号强度并减少光谱干扰。优化了Chelex用于SRM 1598a和阴离子交换用于SRM 3244的色谱分离程序,以实现所需的分离特性,而基本上不增加程序空白。通过使用去溶剂化雾化可以进一步提高测定血清中Cd的灵敏度。我们确定在优化分析条件下,对于SRM 3240,SRM 3241,SRM 3243和SRM 966 L2中的Cd进行精确的ICP-MS测定,不需要分离。将这些样品稀释至最小体积,然后通过低流量(40–100μL/ min)微同心雾化器引入ICP-MS。还直接分析了SRM 966 L1,但结果变化很大。此处描述的ID-ICP-MS样品制备和比率测量方案导致测定SRM 3240中的90.85μgkg?1 Cd时,总扩展不确定度小于1%,总扩展不确定度小于10%用于测定SRM 1598a中0.0468μgkg?1 Cd。

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