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首页> 外文期刊>Journal of chromatography, B. Analytical technologies in the biomedical and life sciences >Determination of multiple human arsenic metabolites employing high performance liquid chromatography inductively coupled plasma mass spectrometry
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Determination of multiple human arsenic metabolites employing high performance liquid chromatography inductively coupled plasma mass spectrometry

机译:高效液相色谱-电感耦合等离子体质谱法测定多种人类砷代谢物

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During the metabolism of different arsenic-containing compounds in human, a variety of metabolites are produced with significantly varying toxicities. Currently available analytical methods can only detect a limited number of human metabolites in biological samples during one run due to their diverse characteristics. In addition, co-elution of species is often unnoticeable with most detection techniques leading to inaccurate metabolic profiles and assessment of toxicity. A high performance liquid chromatography inductively coupled mass spectrometry (HPLC-ICP-MS) method was developed that can identify thirteen common arsenic metabolites possibly present in human with special attention dedicated to thiolated or thiol conjugated arsenicals. The thirteen species included in this study are arsenite (As-III), arsino-glutathione (As(GS)(3)), arsenate (As-v), monomethylarsonous acid (MMA(III)), monomethylarsinoglutathione (MMA(III)(GS)(2)), monomethylarsonic acid (MMA(v)), dimethylarsinous acid (DMA(III) (from DMA(III)I)), S-(dimethylarsinic)cysteine (DMAIII(Cys)), dimethylarsino-glutathione (DMA(III)(GS)), dimethylarsinic acid (DMA(V)), dimethylmonothioarsinic acid (DMMTA(v)), dimethyldithioarsinic acid (DMDTA(v)), dimethylarsinothioyl glutathione (DMMTA(v)(GS)). The developed method was applied for the analysis of cancer cells that were incubated with darinaparsin (DMA(III)(GS)), a novel chemotherapeutic agent for refractory malignancies, and the arsenic metabolic profile obtained was compared to results using a previously developed method. This method provides a useful analytical tool which is much needed in unequivocally identifying the arsenicals formed during the metabolism of environmental arsenic exposure or therapeutic arsenic administration. (C) 2015 Elsevier B.V. All rights reserved.
机译:在人体中不同的含砷化合物代谢过程中,会产生多种代谢物,其毒性差异很大。当前可用的分析方法由于其多样化的特性,一次运行只能检测出生物样品中有限数量的人类代谢物。此外,大多数检测技术通常不会引起物种的共洗脱,从而导致新陈代谢特征和毒性评估不准确。开发了一种高效液相色谱电感耦合质谱法(HPLC-ICP-MS),该方法可以识别人体内可能存在的13种常见砷代谢物,并特别关注硫醇化或硫醇结合的砷化物。这项研究中包括的13种是亚砷酸盐(As-III),砷基谷胱甘肽(As(GS)(3)),砷酸盐(As-v),一甲基ar酸(MMA(III)),一甲基砷基谷胱甘肽(MMA(III)) (GS)(2)),单甲基ar酸(MMA(v)),二甲基ar酸(DMA(III)(来自DMA(III)I)),S-(二甲基ar)半胱氨酸(DMAIII(Cys)),二甲基ar-谷胱甘肽(DMA(III)(GS)),二甲基亚砷酸(DMA(V)),二甲基单硫代砷酸(DMMTA(v)),二甲基二硫代砷酸(DMDTA(v)),二甲基ar硫代酰基谷胱甘肽(DMMTA(v)(GS))。该开发的方法用于分析与抗性恶性肿瘤的新型化学治疗药物darinaparsin(DMA(III)(GS))孵育的癌细胞,并使用先前开发的方法将获得的砷代谢曲线与结果进行了比较。该方法提供了一种有用的分析工具,在明确识别环境砷暴露或治疗性砷给药的新陈代谢过程中形成的砷中非常需要此工具。 (C)2015 Elsevier B.V.保留所有权利。

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