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首页> 外文期刊>Clinical Chemistry: Journal of the American Association for Clinical Chemists >Determination of inorganic arsenic and its organic metabolites in urine by flow-injection hydride generation atomic absorption spectrometry.
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Determination of inorganic arsenic and its organic metabolites in urine by flow-injection hydride generation atomic absorption spectrometry.

机译:流动注射氢化物发生原子吸收光谱法测定尿液中的无机砷及其有机代谢产物。

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A method has been developed for the determination of inorganic arsenic [As(III) and As(V)] and its organic metabolites (monomethylarsenic and dimethylarsenic) in urine by flow-injection hydride generation atomic absorption spectrometry. The nontoxic seafood-derived arsenobetaine and arsenocholine species were first separated by a solid-phase extraction procedure. The remaining sample was digested with a mixture of nitric and sulfuric acids and potassium dichromate, followed by attack with hydrogen peroxide. The resulting As(V) was reduced to As(III) with potassium iodide in hydrochloric acid before injection into the flow-injection manifold. The percentage analytical recoveries (mean +/- 95% confidence interval) of various arsenic species added to a urine specimen at 250 micrograms/L were 108 +/- 2, 112 +/- 11, 104 +/- 7, and 95 +/- 5 for As(III), As(V), monomethylarsenic, and dimethylarsenic, respectively. For the determination of arsenic in Standard Reference Material 2670 (toxic metals in human urine), results agreed with the certified value (480 +/- 100 micrograms/L). Analyses of samples for the Centre de Toxicologie du Quebec, containing seafood-derived species, demonstrated the viability of the separation procedure. Detection limits were between 0.1 and 0.2 microgram/L in the solution injected into the manifold, and precision at 10 micrograms/L was between 2% and 3% (CV). These preliminary results show that the method might be applicable to determinations of arsenic in a range of clinical urine specimens.
机译:开发了一种通过流动注射氢化物发生原子吸收光谱法测定尿中无机砷[As(III)和As(V)]及其有机代谢物(单甲基砷和二甲基砷)的方法。首先通过固相萃取程序分离无毒的海鲜来源的砷甜菜碱和砷胆碱。剩余的样品用硝酸,硫酸和重铬酸钾的混合物消解,然后用过氧化氢侵蚀。在注入流动注射歧管之前,用碘化钾在盐酸中将生成的As(V)还原为As(III)。以250微克/升添加到尿液样本中的各种砷物质的分析回收率(平均+/- 95%置信区间)为108 +/- 2、112 +/- 11、104 +/- 7和95 + -5分别表示As(III),As(V),一甲基砷和二甲基砷。对于标准参考物质2670(人尿中的有毒金属)中砷的测定,结果与认证值一致(480 +/- 100微克/升)。魁北克毒物研究中心的样品分析包含海产品来源的物种,证明了分离程序的可行性。在注入歧管的溶液中,检出限为0.1至0.2微克/升,10微克/升的精密度为2%至3%(CV)。这些初步结果表明,该方法可能适用于测定一系列临床尿液样本中的砷。

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