Georgi Joaudimir Castro, Sommer Yuliya L, Ward Cynthia D, Cheng Po-Yung, Jones Robert L, Caldwell Kathleen L
Inorganic & Radiation Analytical Toxicology Branch, National Center for Environmental Health, Centers for Disease Control and Prevention, 4770 Buford Highway, Mailstop F-50, Atlanta, GA 30341-3717.
Anal Methods. 2017;9(23):3464-3476. doi: 10.1039/C7AY00430C. Epub 2017 Apr 19.
The Centers for Disease Control and Prevention developed a biomonitoring method to rapidly and accurately quantify chromium and cobalt in human whole blood by ICP-MS. Many metal-on-metal hip implants which contain significant amounts of chromium and cobalt are susceptible to metal degradation. This method is used to gather population data about chromium and cobalt exposure of the U.S. population that does not include people that have metal-on-metal hip implants so that reference value can be established for a baseline level in blood. We evaluated parameters such as; helium gas flow rate, choice and composition of the diluent solution for sample preparation, and sample rinse time to determine the optimal conditions for analysis. The limits of detection for chromium and cobalt in blood were determined to be 0.41 and 0.06 μg/L, respectively. Method precision, accuracy, and recovery for this method were determined using quality control material created in-house and historical proficiency testing samples. We conducted experiments to determine if quantitative changes in the method parameters affect the results obtained by changing four parameters while analyzing human whole blood spiked with National Institute of Standard and Technology traceable materials: the dilution factor used during sample preparation, sample rinse time, diluent composition, and kinetic energy discrimination gas flow rate. The results at the increased and decreased levels for each parameter were statistically compared to the results obtained at the optimized parameters. We assessed the degree of reproducibility obtained under a variety of conditions and evaluated the method's robustness by analyzing the same set of proficiency testing samples by different analysts, on different instruments, with different reagents, and on different days. The short-term stability of chromium and cobalt in human blood samples stored at room temperature was monitored over a time period of 64 hours by diluting and analyzing samples at different time intervals. The stability of chromium and cobalt post-dilution was also evaluated over a period of 48 hours and at two storage temperatures (room temperature and refrigerated at 4°C). The results obtained during the stability studies showed that chromium and cobalt are stable in human blood for a period of 64 hours.
美国疾病控制与预防中心开发了一种生物监测方法,通过电感耦合等离子体质谱法(ICP-MS)快速准确地定量测定人体全血中的铬和钴。许多含大量铬和钴的金属对金属髋关节植入物易发生金属降解。该方法用于收集美国人群中铬和钴暴露情况的人口数据,这些人群不包括植入金属对金属髋关节植入物的人,以便为血液中的基线水平建立参考值。我们评估了诸如氦气流速、样品制备稀释剂溶液的选择和成分以及样品冲洗时间等参数,以确定最佳分析条件。血液中铬和钴的检测限分别确定为0.41和0.06μg/L。使用内部创建的质量控制材料和历史能力验证样品确定了该方法的精密度、准确度和回收率。我们进行了实验,通过分析添加了美国国家标准与技术研究院可溯源材料的人体全血,改变四个参数(样品制备过程中使用的稀释因子、样品冲洗时间、稀释剂成分和动能歧视气体流速)来确定方法参数的定量变化是否会影响所得结果。将每个参数增加和减少水平时的结果与优化参数时获得的结果进行统计学比较。我们评估了在各种条件下获得的重现性程度,并通过不同分析人员在不同仪器上使用不同试剂在不同日期分析同一组能力验证样品来评估该方法的稳健性。通过在不同时间间隔稀释和分析样品,在64小时的时间段内监测了室温下储存的人体血液样品中铬和钴的短期稳定性。还在48小时的时间段内以及在两个储存温度(室温以及4°C冷藏)下评估了稀释后铬和钴的稳定性。稳定性研究期间获得的结果表明,铬和钴在人体血液中64小时内是稳定的。