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电热蒸发电感耦合等离子体质谱法测定尿液中的稀土元素

Determination of rare earth elements in urine by electrothermal vaporization inductively coupled plasma mass spectrometry.

作者信息

Bettinelli Maurizio, Spezia Sandro, Terni Cesarina, Ronchi Anna, Balducci Claudio, Minoia Claudio

机构信息

ENEL DP-Central Laboratory of Piacenza, via N. Bixio 39, Piacenza, Italy.

出版信息

Rapid Commun Mass Spectrom. 2002;16(6):579-84. doi: 10.1002/rcm.609.

Abstract

A method was developed for the determination of rare earth elements (REEs) in urine with electrothermal vaporization inductively coupled plasma mass spectrometry (ETV-ICPMS). The undiluted sample was directly injected into the graphite tube and trifluoromethane (Freon-23) was used as chemical modifier in order to reduce the vaporization temperature and the memory effect of most of the lanthanides. The detection limits were in the range 1-10 ng/L with relative standard deviation of 3-5% at concentration levels of 1microg/L, and less than 10-15% at 100 ng/L. Two different procedures, external calibration and a standard additions method, were evaluated to measure the concentration levels of lanthanides in the urine samples and the second procedure was considered to be the best choice for calibration in this work. The level of REEs in urine of 50 healthy volunteers was in the range 5-20 ng/L, above the detection limit of ETV-ICPMS.

摘要

建立了一种用电热蒸发电感耦合等离子体质谱法(ETV-ICPMS)测定尿液中稀土元素(REEs)的方法。未稀释的样品直接注入石墨管,使用三氟甲烷(氟利昂-23)作为化学改性剂,以降低大多数镧系元素的蒸发温度和记忆效应。检测限在1-10 ng/L范围内,在1μg/L浓度水平下相对标准偏差为3-5%,在100 ng/L时小于10-15%。评估了两种不同的程序,即外部校准和标准加入法,以测量尿液样品中镧系元素的浓度水平,第二种程序被认为是本工作中校准的最佳选择。50名健康志愿者尿液中的REEs水平在5-20 ng/L范围内,高于ETV-ICPMS的检测限。

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