Bellis David J, Hetter Katherine M, Verostek Mary Frances, Parsons Patrick J
Trace Elements Laboratory, Wadsworth Center, New York State Department of Health, P.O. Box 509, Albany, NY 12201, USA.
J Anal At Spectrom. 2008;23(3):298-308. doi: 10.1039/B710808G. Epub 2007 Nov 12.
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.
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。