Quantitative analysis of perchlorate in extracts of whole fish homogenates by ion chromatography: comparison of suppressed conductivity detection and electrospray ionization mass spectrometry

被引:25
作者
Dodds, ED
Kennish, JM
von Hippel, FA
Bernhardt, R
Hines, ME
机构
[1] Univ Alaska Anchorage, Dept Chem, Anchorage, AK 99508 USA
[2] Univ Alaska Anchorage, Appl Sci Engn & Technol Lab, Anchorage, AK 99508 USA
[3] Univ Alaska Anchorage, Dept Biol Sci, Anchorage, AK 99508 USA
基金
美国国家科学基金会;
关键词
perchlorate; ion chromatography; suppressed conductivity detection; electrospray ionization mass spectrometry;
D O I
10.1007/s00216-004-2660-8
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The perchlorate anion (ClO4-) is an anthropogenic contaminant of increasing concern in water supplies, and has been shown to disrupt thyroid activity. Most perchlorate analyses are currently carried out by ion chromatography (IC) with suppressed conductivity detection (SCD). While this procedure has been demonstrated to provide acceptable performance for analysis of water samples, the determination of perchlorate in high-conductivity aqueous extracts of plant or animal material is not readily accomplished by IC-SCD unless lengthy cleanup protocols are applied. With the addition of electrospray ionization mass spectrometry (ESI-MS) to IC, it was hypothesized that the interference imposed by various ionic species could be significantly reduced without the need for purification; however, the analysis of perchlorate in relatively unpurified extracts of biologically derived homogenates by IC-ESI-MS has not previously been described in the literature. The research presented here represents a comparison of the capabilities of IC-SCD and IC-ESI-MS to detect perchlorate in reagent water and in crude extracts of perchlorate-exposed fish (threespine stickleback, Gasterosteus aculeatus). ESI-MS was found to compare favorably to SCD for the detection of perchlorate in deionized water, and to exceed SCD performance in perchlorate analysis of fish-derived extracts.
引用
收藏
页码:881 / 887
页数:7
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