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      Recent applications of laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS) for biological sample analysis: a follow-up review

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          Abstract

          Information provided by laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS) in the analysis of biological tissues is expanding.

          Abstract

          Laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS) is a feasible technique to obtain either quantitative elemental data or spatially resolved imaging/mapping of elements in biological tissues. Its popularity is due to the great detection capability of the setup, which has found central applicability in metallomics, nanoparticles uptake, labeling and tagging strategies in biological systems, elemental mapping of tissues and quantitative data for biomedical studies, besides utilization in a complementary manner with molecular mass spectrometry techniques. This article provides an update of recent progress and applications of LA-ICP-MS in the biological field, covering the time frame of the last three years. Key topics dealing with fast wash-out laser ablation cell developments, novel calibration strategies such as ink printing and dried-droplets, applications and mapping of elemental distribution in biological samples (animal, human and plant tissues), nanoparticle uptake, protein and single cell analysis are surveyed and critically discussed.

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          Fast chemical imaging at high spatial resolution by laser ablation inductively coupled plasma mass spectrometry.

          In recent years, chemical imaging was prognosticated to become one of the key analytical applications for laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS). However, moderate spatial resolution and the associated measurement time required for a larger sampling area, have restricted this versatile, high sensitivity technique from being routinely used in two-dimensional chemical imaging. This work describes the development and investigation of a low dispersion sample chamber (tube cell), which allows improvement of the imaging capabilities by reduction of the single LA shot duration to 30 ms (full width at 1% maximum). The new tube cell is based on a constant laminar flow and a well-controlled delivery of the laser-ablated aerosol into the transport system, leading to minimized tailing of the aerosol washout and helping to separate the signals even at repetition rates as high as 20-30 Hz. To demonstrate the improved imaging capabilities, microstructured metallic thin film patterns were analyzed at a spatial resolution of a few micrometers. The LA-ICP-MS results obtained were comparable to Synchrotron-based micro-X-ray fluorescence (SR-microXRF). The suitability of the newly designed cell for multielement acquisitions was demonstrated using a simultaneous ICP-Mattauch-Herzog-MS. Finally, the novel laser ablation cell was applied to image the distribution of a metal-tagged biomarker in a thin section of breast cancer tissue. This application demonstrates that the technique is able to produce subcellular (~1 μm) spatial resolution, which is crucial for morphological assessment in cancer diagnostics.
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            Recent advances in quantitative LA-ICP-MS analysis: challenges and solutions in the life sciences and environmental chemistry

            Laser ablation–inductively coupled plasma–mass spectrometry (LA-ICP-MS) is a widely accepted method for direct sampling of solid materials for trace elemental analysis. The number of reported applications is high and the application range is broad; besides geochemistry, LA-ICP-MS is mostly used in environmental chemistry and the life sciences. This review focuses on the application of LA-ICP-MS for quantification of trace elements in environmental, biological, and medical samples. The fundamental problems of LA-ICP-MS, such as sample-dependent ablation behavior and elemental fractionation, can be even more pronounced in environmental and life science applications as a result of the large variety of sample types and conditions. Besides variations in composition, the range of available sample states is highly diverse, including powders (e.g., soil samples, fly ash), hard tissues (e.g., bones, teeth), soft tissues (e.g., plants, tissue thin-cuts), or liquid samples (e.g., whole blood). Within this article, quantification approaches that have been proposed in the past are critically discussed and compared regarding the results obtained in the applications described. Although a large variety of sample types is discussed within this article, the quantification approaches used are similar for many analytical questions and have only been adapted to the specific questions. Nevertheless, none of them has proven to be a universally applicable method.
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              Imaging metals in biology: balancing sensitivity, selectivity and spatial resolution.

              Metal biochemistry drives a diverse range of cellular processes associated with development, health and disease. Determining metal distribution, concentration and flux defines our understanding of these fundamental processes. A comprehensive analysis of biological systems requires a balance of analytical techniques that inform on metal quantity (sensitivity), chemical state (selectivity) and location (spatial resolution) with a high degree of certainty. A number of approaches are available for imaging metals from whole tissues down to subcellular organelles, as well as mapping metal turnover, protein association and redox state within these structures. Technological advances in micro- and nano-scale imaging are striving to achieve multi-dimensional and in vivo measures of metals while maintaining the native biochemical environment and physiological state. This Tutorial Review discusses state-of-the-art imaging technology as a guide to obtaining novel insight into the biology of metals, with sensitivity, selectivity and spatial resolution in focus.
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                Author and article information

                Journal
                JASPE2
                Journal of Analytical Atomic Spectrometry
                J. Anal. At. Spectrom.
                Royal Society of Chemistry (RSC)
                0267-9477
                1364-5544
                2017
                2017
                : 32
                : 5
                : 890-919
                Affiliations
                [1 ]Instituto de Química
                [2 ]Universidade Federal do Rio grande do Sul
                [3 ]Porto Alegre
                [4 ]Brazil
                [5 ]Departamento de Química
                [6 ]Universidade Federal de Santa Maria
                [7 ]97.105-900 Santa Maria
                Article
                10.1039/C7JA00026J
                1f8a71d4-15b9-44c1-a87d-073072fe3eca
                © 2017
                History

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