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紫外二氧化钛薄膜反应器与液相色谱/氢化物发生/电感耦合等离子体质谱系统的在线联用,用于连续测定极微量微透析样品中氢化物形成和非氢化物形成砷物种的动态变化。

On-line coupling of an ultraviolet titanium dioxide film reactor with a liquid chromatography/hydride generation/inductively coupled plasma mass spectrometry system for continuous determination of dynamic variation of hydride- and nonhydride-forming arsenic species in very small microdialysate samples.

作者信息

Tsai Mine-wei, Sun Yuh-chang

机构信息

Department of Biomedical Engineering and Environmental Sciences, National Tsing-Hua University, Hsinchu, Taiwan.

出版信息

Rapid Commun Mass Spectrom. 2008;22(2):211-6. doi: 10.1002/rcm.3353.

Abstract

We describe a method for continuously monitoring both hydride- and nonhydride-forming arsenic species in 10-microL microdialysate samples by coupling together on-line high-performance liquid chromatography (HPLC), a post-column UV/TiO2 film reactor, and hydride generation (HG) inductively coupled plasma mass spectrometry (ICP-MS). To maximize the signal intensities of the desired arsenic species, we optimized the photocatalytic oxidation efficiency of the analyte species and used a rapid on-line pre-reduction process to convert the oxidized species into As(III) prior to HG-ICP-MS determination. The UV/nano-TiO2 film reactor was manufactured by coating nano-TiO2 onto the interior of a glass tube. Impregnation and sol-gel methods were employed to deposit the TiO2 films, and their effectiveness for the oxidation of organic arsenicals was compared. To enhance the decomposition efficiency of organic arsenicals, we investigated the effects of the acidity and the composition of the column effluent. Because of the improved HG efficiency toward the tested arsenicals and the adoption of a segmented flow technique to retain the peak resolution in our on-line LC-UV/nano-TiO2 film reactor-HG-ICP-MS instrument, the detection limits for arseneous acid [As(III)], monomethylarsonic acid (MMA), dimethylarsinic acid (DMA), arsenic acid [As(V)], and arsenobetaine (AsB) were all in the submicrogram-per-liter range (based on 3 sigma) for 10-microL injections. A series of validation experiments--analyses of certified reference urine and rabbit serum samples--indicated that these methods can be applied satisfactorily to the continuous determination of As(III), MMA, DMA, As(V), and AsB in blood and in the extracellular space of target organs.

摘要

我们描述了一种通过在线高效液相色谱(HPLC)、柱后紫外/二氧化钛薄膜反应器和氢化物发生(HG)电感耦合等离子体质谱(ICP-MS)联用,对10微升微透析液样品中氢化物形成型和非氢化物形成型砷物种进行连续监测的方法。为了使所需砷物种的信号强度最大化,我们优化了分析物物种的光催化氧化效率,并在HG-ICP-MS测定之前采用快速在线预还原过程,将氧化态物种转化为As(III)。紫外/纳米二氧化钛薄膜反应器是通过将纳米二氧化钛涂覆在玻璃管内部制成的。采用浸渍法和溶胶-凝胶法沉积二氧化钛薄膜,并比较了它们对有机砷化合物的氧化效果。为了提高有机砷化合物的分解效率,我们研究了柱流出物酸度和组成的影响。由于我们的在线LC-紫外/纳米二氧化钛薄膜反应器-HG-ICP-MS仪器对测试砷化合物的HG效率提高,以及采用了分段流动技术来保持峰分辨率,对于10微升进样量,亚砷酸[As(III)]、一甲基砷酸(MMA)、二甲基砷酸(DMA)、砷酸[As(V)]和砷甜菜碱(AsB)的检测限均在每升亚微克范围内(基于3σ)。一系列验证实验——对有证参考尿液和兔血清样品的分析——表明这些方法可令人满意地应用于血液和靶器官细胞外空间中As(III)、MMA、DMA、As(V)和AsB的连续测定。

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