A high-throughput microdialysis-parallel solid phase extraction-inductively coupled plasma mass spectrometry hyphenated system for continuous monitoring of extracellular metal ions in living rat brain

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Abstract

To significantly improve the temporal resolving power of in vivo trace brain metal monitoring system, in this paper we describe a novel analytical configuration combining the dual functions of online segmentation of the rat brain microdialysate and parallel solid phase extraction (SPE) of multiple segmented samples. In contrast to traditional SPE procedures, in this study the three pumped media-the buffered rat brain microdialysate, the eluent, and the air stream-were converted to a series of segmented streams through the manipulation of a flow-through stream selector. After optimizing this online automatic MD/parallel poly(vinyl chloride) SPE/inductively coupled plasma mass spectrometry hyphenated system for the analysis of ultra-trace metal ions, the sample volume of the microdialysate was set at 0.83μL, the analytical sequence was repeatable every 20s, and the detection limits were in the range 0.03-0.24μgL-1, with spike analyses of Mn, Co, Ni, Cu, and Zn in a rat brain ECF sample agreeing well with expected values (88-107%). To further examine the system's practicability, we also performed (i) in vivo dynamic monitoring of these trace metal ions in living rat brain extracellular fluid post-probe implantation (the basal values for Mn, Co, Ni, Cu, and Zn were 1.17±0.18, 1.27±0.36, 2.46±0.62, 0.86±0.37, and 2.35±0.55μgL-1, respectively) and (ii) real-time visualization of the physiological response to acute neural depolarization elicited upon perfusing a high-K+ medium through the MD probe. © 2013 Elsevier B.V.

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Su, C. K., Hsia, S. C., & Sun, Y. C. (2014). A high-throughput microdialysis-parallel solid phase extraction-inductively coupled plasma mass spectrometry hyphenated system for continuous monitoring of extracellular metal ions in living rat brain. Journal of Chromatography A, 1326, 73–79. https://doi.org/10.1016/j.chroma.2013.12.047

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