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Cerebrospinal fluid elemental analysis by using a total sample consumption system operated at high temperature adapted to inductively coupled plasma mass spectrometry

机译:通过使用在高温下运行的适用于感应耦合等离子体质谱的总样品消耗系统进行脑脊液元素分析

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摘要

A total consumption low sample introduction system has been applied for the first time to the multielement analysis of non-diluted cerebrospinal fluids (CSFs) by means of inductively coupled plasma mass spectrometry (ICP-MS). A 2.5 μL sample volume has been injected into an air carrier stream in agreement with the air-segmented injection principle. The sample plug has been turned into an aerosol by means of a high efficiency nebulizer (HEN) and further introduced into the so-called high temperature torch integrated sample introduction system (hTISIS). A transient signal has been thus obtained. For spiked CSF real samples it has been verified that the higher the temperature, the greater the sensitivity. Under optimized conditions, the hTISIS provides peak areas around four times higher than those provided by the spectrometer default device (i.e., a double pass spray chamber). Additional advantages provided by the former system include limits of detection up to 6 times lower and narrower peaks as compared to those reported for the double pass spray chamber. Furthermore, the use of the hTISIS is not detrimental from the point of view oxide production and doubly charged ion generation. Regarding the extent of non-spectral interference caused by the CSF matrix, it has been verified that, with the hTISIS, recoveries for spiked real samples were close to 100% for a set of 14 different elements (V, Cr, Mn, Co, Ni, Cu, As, Se, Mo, Cd, Sb, Ba, Tl and Pb). Meanwhile, in segmented flow injection mode, the reference system provided recoveries from 200 to 500%, depending on the element and the sample, thus demonstrating the occurrence of matrix effects.
机译:总消耗量低的样品引入系统已首次通过电感耦合等离子体质谱法(ICP-MS)应用于未稀释的脑脊液(CSF)的多元素分析。按照空气分段进样原理,已将2.5μL的样品量注入空气流中。样品塞已通过高效雾化器(HEN)转化为气雾剂,并进一步引入了所谓的高温炬炬集成样品引入系统(hTISIS)。由此获得了瞬态信号。对于加标的CSF真实样品,已证实温度越高,灵敏度越高。在最佳条件下,hTISIS提供的峰面积比光谱仪默认设备(即双通道喷雾室)提供的峰面积高大约四倍。前者系统提供的其他优点包括与双通道喷雾腔室报告的峰相比,检测极限最高可降低6倍且峰较窄。此外,从氧化物产生和双电荷离子产生的角度来看,hTISIS的使用无害。关于CSF矩阵引起的非光谱干扰的程度,已经验证了通过hTISIS,对于14种不同元素(V,Cr,Mn,Co, Ni,Cu,As,Se,Mo,Cd,Sb,Ba,Tl和Pb)。同时,在分段流动注射模式下,参考系统提供的回收率从200%到500%(取决于元素和样品),从而证明了基质效应的发生。

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