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Quantitative laser-induced breakdown spectroscopy analysis of calcified tissue samples
Affiliation:1. Central European Institute of Technology, Brno University of Technology, Purkyňova 656/123, CZ-61200 Brno, Czech Republic;2. AtomTrace a.s., Kolejní 9, CZ-61200 Brno, Czech Republic;3. Department of Mechanical and Aerospace Engineering, University of Florida, 939 Sweetwater Drive, FL-32611 Gainesville, FL, USA;1. Department of Hematology, Harbin Medical University Cancer Hospital, Harbin 150081, China;2. National Key Laboratory of Science and Technology on Tunable Laser, Harbin Institute of Technology, Harbin 150080, China;3. Institute of Opto-electronics, Harbin Institute of Technology, Harbin 150080, China
Abstract:We report on the application of laser-induced breakdown spectroscopy (LIBS) to the analysis of important minerals and the accumulation of potentially toxic elements in calcified tissue, to trace e.g. the influence of environmental exposure, and other medical or biological factors. This theme was exemplified for quantitative detection and mapping of Al, Pb and Sr in representative samples, including teeth (first teeth of infants, second teeth of children and teeth of adults) and bones (tibia and femur). In addition to identifying and quantifying major and trace elements in the tissues, one- and two-dimensional profiles and maps were generated. Such maps (a) provide time/concentration relations, (b) allow to follow mineralisation of the hydroxyapatite matrix and the migration of the elements within it and (c) enable to identify disease states, such as caries in teeth. In order to obtain quantitative calibration, reference samples in the form of pressed pellets with calcified tissue-equivalent material (majority compound of pellets is CaCO3) were used whose physical properties closely resembled hydroxyapatite. Compounds of Al, Sr and Pb were added to the pellets, containing atomic concentrations in the range 100–10 000 ppm relative to the Ca content of the matrix. Analytical results based on this calibration against artificial samples for the trace elements under investigation agree with literature values, and with our atomic absorption spectroscopy (AAS) cross-validation measurements.
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