【24h】

Candidate BCR reference materials for arsenic and selenium determinations in human serum and urine

机译:人体血清和尿液中砷和硒测定的候选BCR参考材料

获取原文
获取原文并翻译 | 示例

摘要

The pilot production of candidate reference materials for the quality assurance and statistical control of methods to determine toxic trace elements in biological samples is described. In the initial phase the project concerns a lyophilized human blood material containing Cd and Pb, a lyophilized human urine material containing As, Cd, Co and Cr, and a liquid human serum material with Al, Se and Zn at three different levels, representative of environmental and occupational exposure. The homogeneity and stability of the pilot batches were investigated by determining Al and Zn in serum, As in urine, Cd and Pb in blood at the medium level. The pilot batches produced were deemed to be homogeneous with respect to all the trace elements tested, and there was no indication of thermal instability except that the arsenic levels decreased significantly with time at 200 dec, 370 deg and 450 deg. Thirty-two laboratories from 12 different countries participated in an intercomparison round organized to test the suitability of the reference material and validate the methodological approaches for certification purposes. Focusing on the neutron activation results, the outcome of this first intercom-parison exercise demonstrates that the comparability of the calibration standards needs improvement. There fore, for the certification round stronger efforts will be undertaken to document the spiked concentrations and to reduce their uncertainties, and the laboratories will be required to meet defined quality criteria for the checking and documentation of traceability.
机译:描述了用于质量保证和统计控制以确定生物样品中有毒微量元素的方法的候选参考材料的试生产。在最初阶段,该项目涉及含有Cd和Pb的冻干人血材料,含有As,Cd,Co和Cr的冻干人尿材料以及具有三种不同水平的Al,Se和Zn的液态人血清材料,代表环境和职业暴露。通过测定中等水平的血清中的Al和Zn,尿液中的As,血液中的Cd和Pb来研究中试批次的均质性和稳定性。相对于所有测试的痕量元素,生产的中试批次被认为是均质的,除了砷含量在200 dec,370 deg和450 deg随时间显着降低外,没有热不稳定性的迹象。来自12个不同国家的32个实验室参加了一次比对活动,目的是测试标准物质的适用性并验证用于认证目的的方法。着眼于中子活化结果,第一次内部比较实验的结果表明,校准标准品的可比性需要改善。因此,在认证轮次中,将采取更大的努力来记录加标浓度并减少其不确定性,并且将要求实验室符合定义的质量标准,以进行可检查性和可追溯性检查。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号