In vivo monitoring of multiple trace metals on the brain extracellular fluid of anesthetized rats by microdialysis-membrane Desalter-ICPMS

被引:28
作者
Chung, Y. T.
Ling, Y. C.
Yang, C. S.
Sun, Y. C. [1 ]
Lee, P. L.
Lin, C. Y.
Hong, C. C.
Yang, M. H.
机构
[1] Natl Tsing Hua Univ, Dept Biomed Engn & Environm Sci, Hsinchu, Taiwan
[2] Natl Tsing Hua Univ, Dept Chem, Hsinchu, Taiwan
[3] Natl Chi Nan Univ, Dept Appl Chem, Nantou, Taiwan
关键词
D O I
10.1021/ac070981z
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
We have developed an on-line analytical system involving microdialysis (MD) sampling, a carbohydrate membrane desalter (CMD), and an inductively coupled plasma mass spectrometer (ICPMS) system for the simultaneous determination of multiple trace metals in the extracellular fluid (ECF) in the brains of anesthetized rats. The microdialysate that perfused from the animal at a Row rate of 0.5 mu L/min was on-line transferred to the CMD to remove the high-sodium matrix, followed by ICPMS measurement. The role of the CMD in this on-line system was investigated in detail. With prior addition of EDTA to the microdialysate to form anionic complexes' of the metal analytes and the use of NH4Cl as a regenerant to exchange Na+ with NH4+ ions, both quantitative recovery of the trace metal analytes and quantitative removal of the sodium matrix could be achieved. Two experimental modes of the monitoring system were constructed. For those metals (e.g., Cu, Zn, and Mn) that existed at (sub)nanogram-permilliliter concentrations in the microdialysate, the temporal resolution was 10 min when using a 10 mu L loop for sample collection, followed by CMD and ICPMS; for those elements (e.g., Ca and Mg) that existed at microgram-permilliliter levels (or greater), near-real-time analysis was possible because the microdialysate could be led, bypassing the sample loop, directly to the CMD for desalting without any time delay. Further improvement of the temporal resolution for the low-concentration elements was not possible without decreasing the detection limits of mass detection. Among the eight trace metals tested using this on-line system, the method detection limits for Cu, Zn, Mn, Co, Ni, and Ph reached subnanogram-permilliliter levels; for electrolyte species such as Ca and Mg, the detection limits were in the range of 50 - 100 mu g/mL. Analytical accuracy, expressed as spike recovery, was 100% +/- 15% for all of the elements tested. We demonstrate the applicability of the proposed system through the successful measurement of the basal values of Ca, Mg, Cu, Zn, and Mn in the ECF of a living rat brain and through in vivo monitoring of the concentration profiles of Mn and Pt in the ECF after the injection of drugs (MnCl2 and cisplatin) into the rats. This microdialysis system is the first to offer real-time, in vivo monitoring of trace elements such as Ca and Mg.
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页码:8900 / 8910
页数:11
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