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通过实验室间研究和双同位素稀释质谱法对骨铅候选参考物质进行表征。

Characterization of candidate reference materials for bone lead via interlaboratory study and double isotope dilution mass spectrometry.

作者信息

Bellis David J, Hetter Katherine M, Verostek Mary Frances, Parsons Patrick J

机构信息

Trace Elements Laboratory, Wadsworth Center, New York State Department of Health, P.O. Box 509, Albany, NY 12201, USA.

出版信息

J Anal At Spectrom. 2008;23(3):298-308. doi: 10.1039/B710808G. Epub 2007 Nov 12.

Abstract

Four candidate ground bone reference materials (NYS RMs 05-01 through 04), were produced from lead-dosed bovine and caprine sources, and characterized by interlaboratory study. The consensus value ( X ) and expanded standard uncertainty (U(X) ) were determined from the robust average and standard deviation of the participants' data for each NYS RM 05-01 through 04. The values were 1.08 ±0.04, 15.3 ±0.5, 12.4 ±0.5, and 29.9 ±1.1 μg g(-1) Pb, respectively. Youden plots of z-scores showed a statistically significant correlation between the results for pairs of NYS RM 05-02 through 04, indicating common sources of between-laboratory variation affecting reproducibility. NYS RM 05-01 exhibited more random variability affecting repeatability at low concentration. Some participants using electrothermal atomic absorption spectrometry (ETAAS) exhibited a negative bias compared to the all-method consensus value. Other methods used included inductively coupled plasma mass spectrometry (ICP-MS), isotope dilution (ID-) ICP-MS, and ICP atomic (optical) emission spectroscopy (-OES). The NYS RMs 05-01 through 04 were subsequently re-analyzed in house using double ID-ICP-MS to assign certified reference values (C ) and expanded uncertainty (U(C) ) of 1.09 ± 0.03, 16.1 ± 0.3, 13.2 ± 0.3 and 31.5 ± 0.7, respectively, indicating a low bias in the interlaboratory data. SRM 1486 Bone Meal was analyzed for measurement quality assessment obtaining results in agreement with the certified values within the stated uncertainty. Analysis using a primary reference method based on ID-ICP-MS with full quantification of uncertainty calculated according to ISO guidelines provided traceability to SI units.

摘要

四种候选骨粉标准物质(纽约州标准物质05 - 01至04)由经铅处理的牛和羊来源制备,并通过实验室间研究进行了表征。通过对纽约州标准物质05 - 01至04的参与者数据进行稳健平均和标准差计算,确定了其一致性值(X)和扩展标准不确定度(U(X))。这些值分别为1.08±0.04、15.3±0.5、12.4±0.5和29.9±1.1μg g⁻¹ Pb。z分数的尤登图显示,纽约州标准物质05 - 02至04的结果之间存在统计学上显著的相关性,表明影响再现性的实验室间变异存在共同来源。纽约州标准物质05 - 01在低浓度下表现出更多影响重复性的随机变异性。一些使用电热原子吸收光谱法(ETAAS)的参与者与所有方法的一致性值相比存在负偏差。使用的其他方法包括电感耦合等离子体质谱法(ICP - MS)、同位素稀释(ID -)ICP - MS和ICP原子(光学)发射光谱法(-OES)。随后在内部使用双ID - ICP - MS对纽约州标准物质05 - 01至04进行重新分析,以确定其认证参考值(C)和扩展不确定度(U(C)),分别为1.09±0.03、16.1±0.3、13.2±0.3和31.5±0.7,表明实验室间数据存在低偏差。对标准参考物质1486骨粉进行了分析以评估测量质量,所获结果在规定不确定度范围内与认证值一致。使用基于ID - ICP - MS的主要参考方法并根据ISO指南对不确定度进行全面量化分析,实现了溯源至国际单位制(SI)单位。

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