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对单颗粒 ICP-MS 数据处理中关键参数的批判性评估,以正确测定复杂环境和生物基质中的铂纳米粒子。

Critical evaluation of key parameters in single particle ICP-MS data processing for the correct determination of platinum nanoparticles in complex environmental and biological matrices.

机构信息

Department of Analytical Chemistry and Food Technology, Environmental Sciences Institute (ICAM), University of Castilla-La Mancha, Avda. Carlos III s/n, 45071, Toledo, Spain.

出版信息

Mikrochim Acta. 2023 Nov 23;190(12):476. doi: 10.1007/s00604-023-06032-2.

Abstract

There is an urgent need for the harmonization of critical parameters in single particle inductively coupled plasma mass spectrometry (SP-ICP-MS) and they have been deeply studied and optimized in the present work using platinum nanoparticles (PtNPs) as a representative case of study. Special attention has been paid to data processing in order to achieve an adequate discrimination between signals. Thus, a comparison between four different algorithms has been performed and the method for transport efficiency calculation has also been thorougly evaluated (finding the use of a well-characterized solution of the same targeted analyte (30 nm PtNPs) as adequate). The best results have been obtained after the application of a deconvolution approach for the data processing and using 5 ms as dwell time and 40,000 data points for data acquisition. Under the optimized conditions, a correct discrimination between NP events and background signal up to 100 or 750 ng L of added ionic Pt was reached for 30 and 50 nm PtNPs, respectively. The suitability of the developed method for the characterization of PtNPs in relevant environmental (water samples) and biological (cell culture media) matrices has also been demonstrated.

摘要

目前非常需要协调单颗粒电感耦合等离子体质谱(SP-ICP-MS)中的关键参数,本工作使用铂纳米颗粒(PtNPs)作为研究实例,对其进行了深入研究和优化。特别关注数据处理,以实现信号的充分区分。因此,对四种不同算法进行了比较,并对传输效率计算方法进行了全面评估(发现使用相同目标分析物(30nm PtNPs)的特征良好的溶液作为合适的方法)。在对数据进行去卷积处理并使用 5ms 的停留时间和 40000 个数据点进行数据采集后,得到了最佳结果。在优化条件下,对于 30nm 和 50nm PtNPs,分别可以正确区分高达 100ng/L 或 750ng/L 添加离子态 Pt 的纳米颗粒事件和背景信号。还证明了该方法在相关环境(水样)和生物(细胞培养介质)基质中对 PtNPs 进行表征的适用性。

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