Andrés Suárez Priede, Mario Corte-Rodríguez, Hannes Gödde, María Montes Bayón, Jörg Bettmer
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引用次数: 0
Abstract
Inductively coupled plasma-mass spectrometry (ICP-MS) operated in the single particle (sp) and singe cell (sc) modes belongs to the methods of elemental analysis that has significantly grown during the last years. Its contribution to the characterisation of nanomaterials and cell populations has opened new avenues and possibilities in many different disciplines. In this context, pneumatic nebulisation plays a pivotal role since it is still the preferable sample introduction system in ICP-MS. Reliable quantitative data are only accessible with known transport efficiency (TE) of the small objects, so that the determination of this parameter is extremely critical. In this study, we investigated various combinations of commercially available nebulizers and spray chambers for testing their performance in sp- and sc-ICP-MS. Two configurations made use of high sample flow rates of 0.4 mL/min with a "traditional" cyclonic spray chamber, and another four combinations employed spray chambers especially designed for total consumption used at optimum flow rates of 10 μL/min (Cytospray and HE-SIS). Achievable sensitivities were significantly better for the high consumption set-ups (about 5-fold). Transport efficiencies determined by the particle number method were evaluated by the use of three different model suspensions: i) 30 nm standard gold nanoparticles LGCQC5050, ii) europium-loaded polystyrene beads, and iii) selenized yeast SELM-1. Significant differences between the three suspensions were observed obtaining results up to 90 % for certain configurations. In fact, these differences imply that for different approaches (sp- or sc-ICP-MS) a suitable calibrant has to be used for the accurate determination of the transport efficiency.
期刊介绍:
Talanta provides a forum for the publication of original research papers, short communications, and critical reviews in all branches of pure and applied analytical chemistry. Papers are evaluated based on established guidelines, including the fundamental nature of the study, scientific novelty, substantial improvement or advantage over existing technology or methods, and demonstrated analytical applicability. Original research papers on fundamental studies, and on novel sensor and instrumentation developments, are encouraged. Novel or improved applications in areas such as clinical and biological chemistry, environmental analysis, geochemistry, materials science and engineering, and analytical platforms for omics development are welcome.
Analytical performance of methods should be determined, including interference and matrix effects, and methods should be validated by comparison with a standard method, or analysis of a certified reference material. Simple spiking recoveries may not be sufficient. The developed method should especially comprise information on selectivity, sensitivity, detection limits, accuracy, and reliability. However, applying official validation or robustness studies to a routine method or technique does not necessarily constitute novelty. Proper statistical treatment of the data should be provided. Relevant literature should be cited, including related publications by the authors, and authors should discuss how their proposed methodology compares with previously reported methods.