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本文引用的文献

1
Arsenic (+3 oxidation state) methyltransferase genotype affects steady-state distribution and clearance of arsenic in arsenate-treated mice.砷 (+3 氧化态) 甲基转移酶基因型影响砷酸盐处理小鼠中砷的稳态分布和清除。
Toxicol Appl Pharmacol. 2010 Dec 15;249(3):217-23. doi: 10.1016/j.taap.2010.09.017. Epub 2010 Sep 29.
2
Speciation of arsenic in exfoliated urinary bladder epithelial cells from individuals exposed to arsenic in drinking water.饮用水中砷暴露个体脱落膀胱上皮细胞中砷的形态分析
Environ Health Perspect. 2008 Dec;116(12):1656-60. doi: 10.1289/ehp.11503. Epub 2008 Jul 18.
3
Speciation of arsenic in body fluids.体液中砷的形态分析。
Talanta. 2002 Aug 16;58(1):111-9. doi: 10.1016/s0039-9140(02)00260-6.
4
Tissue distribution and urinary excretion of inorganic arsenic and its methylated metabolites in C57BL6 mice following subchronic exposure to arsenate in drinking water.C57BL6小鼠在亚慢性饮用含砷酸盐的水后,无机砷及其甲基化代谢产物的组织分布和尿排泄情况。
Toxicol Appl Pharmacol. 2008 Nov 1;232(3):448-55. doi: 10.1016/j.taap.2008.07.018. Epub 2008 Jul 28.
5
Speciation analysis of arsenic in biological matrices by automated hydride generation-cryotrapping-atomic absorption spectrometry with multiple microflame quartz tube atomizer (multiatomizer).采用带有多微火焰石英管雾化器(多雾化器)的自动氢化物发生-低温捕集-原子吸收光谱法对生物基质中的砷进行形态分析。
J Anal At Spectrom. 2008;23:342-351. doi: 10.1039/b706144g.
6
Oxidation State Specific Generation of Arsines from Methylated Arsenicals Based on L- Cysteine Treatment in Buffered Media for Speciation Analysis by Hydride Generation - Automated Cryotrapping - Gas Chromatography-Atomic Absorption Spectrometry with the Multiatomizer.基于在缓冲介质中用L-半胱氨酸处理甲基化砷化合物以通过氢化物发生-自动低温捕集-气相色谱-多原子化器原子吸收光谱法进行形态分析,实现特定氧化态砷化氢的生成
Spectrochim Acta Part B At Spectrosc. 2008 Mar;63(3):396-406. doi: 10.1016/j.sab.2007.11.037.
7
A review of the epidemiologic literature on the role of environmental arsenic exposure and cardiovascular diseases.一篇关于环境砷暴露与心血管疾病关系的流行病学文献综述。
Toxicol Appl Pharmacol. 2007 Aug 1;222(3):315-26. doi: 10.1016/j.taap.2006.12.022. Epub 2006 Dec 30.
8
Arsenic exposure and type 2 diabetes: a systematic review of the experimental and epidemiological evidence.砷暴露与2型糖尿病:对实验和流行病学证据的系统综述
Environ Health Perspect. 2006 May;114(5):641-8. doi: 10.1289/ehp.8551.
9
Tissue dosimetry, metabolism and excretion of pentavalent and trivalent monomethylated arsenic in mice after oral administration.口服给药后小鼠体内五价和三价一甲基砷的组织剂量学、代谢及排泄
Toxicol Appl Pharmacol. 2005 Oct 15;208(2):186-97. doi: 10.1016/j.taap.2005.02.008.
10
Urinary trivalent methylated arsenic species in a population chronically exposed to inorganic arsenic.长期接触无机砷人群中的尿三价甲基化砷物种
Environ Health Perspect. 2005 Mar;113(3):250-4. doi: 10.1289/ehp.7519.

氢化物发生-冷阱捕集-原子吸收光谱法直接分析小鼠肝中甲基化三价砷。

Direct analysis of methylated trivalent arsenicals in mouse liver by hydride generation-cryotrapping-atomic absorption spectrometry.

机构信息

Curriculum in Toxicology, University of North Carolina at Chapel Hill, NC, USA.

出版信息

Chem Res Toxicol. 2011 Apr 18;24(4):478-80. doi: 10.1021/tx200060c. Epub 2011 Mar 11.

DOI:10.1021/tx200060c
PMID:21361335
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4154318/
Abstract

Growing evidence suggest that the methylated trivalent metabolites of inorganic arsenic (iAs), methylarsonite (MAs(III)) and dimethylarsinite (DMAs(III)), contribute to adverse effects of iAs exposure. However, the lack of suitable methods has hindered the quantitative analysis of MAs(III) and DMAs(III) in complex biological matrices. Here, we show that hydride generation-cryotrapping-atomic absorption spectrometry can quantify both MAs(III) and DMAs(III) in livers of mice exposed to iAs. No sample extraction is required, thus limiting MAs(III) or DMAs(III) oxidation prior to analysis. The limits of detection are below 6 ng As/g of tissue, making this method suitable even for studies examining low exposures to iAs.

摘要

越来越多的证据表明,无机砷(iAs)的三价甲基代谢物,即甲基胂酸(MAs(III))和二甲基砷酸(DMAs(III)),会导致 iAs 暴露的不良影响。然而,缺乏合适的方法阻碍了复杂生物基质中 MAs(III)和 DMAs(III)的定量分析。在这里,我们展示了氢化物发生-冷阱-原子吸收光谱法可以定量分析 iAs 暴露的小鼠肝脏中的 MAs(III)和 DMAs(III)。不需要样品提取,从而限制了分析前 MAs(III)或 DMAs(III)的氧化。检测限低于 6 ng As/g 组织,即使是研究 iAs 低暴露的研究也非常适用。