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微波消解或干灰化消解后钙补充剂中钙的电感耦合等离子体原子发射光谱法测定及铅的石墨炉原子吸收光谱法测定:方法试验

Determination of calcium by inductively coupled plasma-atomic emission spectrometry, and lead by graphite furnace atomic absorption spectrometry, in calcium supplements after microwave dissolution or dry-ash digestion: method trial.

作者信息

Siitonen P H, Thompson H C

机构信息

U.S. Food and Drug Administration, National Center for Toxicological Research, Jefferson, AR 72079, USA.

出版信息

J AOAC Int. 1998 Nov-Dec;81(6):1233-9.

PMID:9850585
Abstract

A 3-laboratory method trial was conducted to evaluate 2 sample digestion procedures and instrumental determination parameters for analysis of calcium and lead in Ca supplements. Calcium supplements were treated by dry-ash digestion or microwave dissolution prior to spectrometric analysis. In each case, Pb was determined by graphite furnace atomic absorption spectrometry and Ca by inductively coupled plasma-atomic emission spectrometry. Blind duplicates of 6 Ca supplement samples were analyzed after each sample treatment procedure. Matrix pairs contained dissimilar Pb levels to cover the analyte range encountered during method development. Calcium content of the Ca supplement samples also reflected the range seen during method development. Stock solutions of Ca and Pb were supplied to collaborators for preparation of quantitation standards to remove a variable external to the method. National Institute of Standards and Technology Standard Reference Material (NIST SRM) 1486, bone meal, was included to assess method accuracy and recovery at NIST certificate Ca and Pb levels for this material (26.58 +/- 0.24% Ca and 1.335 +/- 0.014 micrograms Pb/g). Analyses of the NIST SRM yielded 25.9 +/- 1.1 and 27.2 +/- 2.3% Ca and 1.53 +/- 0.19 and 1.26 +/- 0.19 micrograms Pb/g for dry-ash and microwave procedures, respectively. Statistical analyses of data indicated acceptable repeatability and reproducibility for determination of Pb and Ca in various Ca supplements. With either sample preparation technique, the method is appropriate for determining Pb or Ca in Ca supplements.

摘要

进行了一项三实验室方法试验,以评估两种样品消解程序和仪器测定参数,用于分析钙补充剂中的钙和铅。在光谱分析之前,钙补充剂通过干灰化消解或微波溶解进行处理。在每种情况下,铅通过石墨炉原子吸收光谱法测定,钙通过电感耦合等离子体原子发射光谱法测定。在每个样品处理程序之后,对6个钙补充剂样品的盲样重复进行分析。基质对含有不同的铅水平,以覆盖方法开发过程中遇到的分析物范围。钙补充剂样品的钙含量也反映了方法开发过程中观察到的范围。向合作者提供钙和铅的储备溶液,用于制备定量标准品,以消除方法外部的变量。包括国家标准与技术研究院标准参考物质(NIST SRM)1486骨粉,以评估该物质在NIST认证的钙和铅水平下的方法准确性和回收率(26.58±0.24%钙和1.335±0.014微克铅/克)。对NIST SRM的分析得出,干灰化法和微波法的钙含量分别为25.9±1.1%和27.2±2.3%,铅含量分别为1.53±0.19微克/克和1.26±0.19微克/克。数据的统计分析表明,测定各种钙补充剂中的铅和钙具有可接受的重复性和再现性。无论采用哪种样品制备技术,该方法都适用于测定钙补充剂中的铅或钙。

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