Comparison of laser ablation-inductively coupled plasma-mass spectrometry and micro-X-ray fluorescence spectrometry for elemental imaging in Daphnia magna

被引:61
作者
Gholap, Deepti S. [1 ]
Izmer, Andrei [1 ]
De Samber, Bjoern [1 ]
van Elteren, Johannes T. [2 ]
Selih, Vid S. [2 ]
Evens, Roel [3 ]
De Schamphelaere, Karel [3 ]
Janssen, Colin [3 ]
Balcaen, Lieve [1 ]
Lindemann, Inge [1 ]
Vincze, Laszlo [1 ]
Vanhaecke, Frank [1 ]
机构
[1] Univ Ghent, Dept Analyt Chem, B-9000 Ghent, Belgium
[2] Natl Inst Chem, Analyt Chem Lab, Ljubljana 1001, Slovenia
[3] Univ Ghent, Lab Environm Toxicol & Aquat Ecol, B-9000 Ghent, Belgium
关键词
Elemental imaging; LA-ICP-MS; Laboratory micro-XRF; Daphnia magna; LA-ICP-MS; ZINC; TOXICITY; EXPOSURE; COMBINATION; SYNCHROTRON; WATERBORNE; TISSUES; SAMPLES; COPPER;
D O I
10.1016/j.aca.2010.01.052
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Visualization of elemental distributions in thin sections of biological tissue is gaining importance in many disciplines of biological and medical research. laser ablation-inductively coupled plasma-mass spectrometry (LA-ICP-MS) and scanning micro-X-ray fluorescence spectrometry (micro-XRF) are two widely used microanalytical techniques for elemental mapping. This article compares the capabilities of the two techniques for imaging the distribution of selected elements in the model organism Daphnia magna in terms of detection power and spatial resolution. Sections with a thickness of 10 and 20 mu m of the fresh water crustacean Daphnia magna were subjected to LA-ICP-MS and micro-XRF analysis. The elemental distributions obtained for Ca, P, S and Zn allow element-to-tissue correlation. LA-ICP-MS and micro-XRF offer similar limits of detection for the elements Ca and P and thus, allow a cross-validation of the imaging results. LA-ICP-MS was particularly sensitive for determining Zn (LOD 20 mu gg(-1), 15 mu m spot size) in Daphnia magna, while the detection power of micro-XRF was insufficient in this context. However, LA-ICP-MS was inadequate for the measurement of the S distributions, which could be better visualized with micro-XRF (LOD 160 mu gg(-1), 5s live time). Both techniques are thus complementary in providing an exhaustive chemical profiling of tissue samples. (C) 2010 Elsevier B.V. All rights reserved.
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页码:19 / 26
页数:8
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