首页> 外文期刊>Australian Journal of Chemistry: A Journal for the Publication of Original Research in All Branches of Chemistry >Arsenic species determination in biological tissues by HPLC-ICP-MS and HPLC-HG-ICP-MS
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Arsenic species determination in biological tissues by HPLC-ICP-MS and HPLC-HG-ICP-MS

机译:HPLC-ICP-MS和HPLC-HG-ICP-MS测定生物组织中的砷种类

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摘要

The use of high-pressure liquid chromatography coupled directly or by a hydride generation system to an inductively coupled plasma mass spectrometer for the unambiguous measurement of 13 arsenic species in marine biological extracts is described. The use of two chromatography systems; a Supelcosil LC-SCX cation-exchange column eluted with a 20 mM pyridine mobile phase adjusted to pH 2.2 and 2.6 with formic acid, with a flow rate of 1.5 mL min(-1) at 40degreesC, and a Hamilton PRP-X100 anion-exchange column eluted with 20 mM NH4H2PO4 buffer at pH 5.6, with a flow rate of 1.5 mL min(-1) at 40degreesC, was required to separate and quantify cation and anion arsenic species. Under these conditions, arsenous acid could not be separated from other arsenic species and required the use of an additional hydride generation step. Arsenic species concentrations in a locally available Tasmania kelp (Durvillea potatorum), a certified reference material (DORM-2), and a range of commercially available macroalgae supplements and sushi seaweeds have been measured and are provided for use as in-house quality control samples to assess the effectiveness of sample preparation, extraction, and measurement techniques.
机译:描述了将高压液相色谱法直接或通过氢化物发生系统与电感耦合等离子体质谱仪耦合使用,以明确测量海洋生物提取物中的13种砷。使用两种色谱系统; Supelcosil LC-SCX阳离子交换柱,用20 mM吡啶流动相用甲酸调节至pH 2.2和2.6,在40°C下流速为1.5 mL min(-1)洗脱,并使用Hamilton PRP-X100阴离子-需要用pH 5.6的20 mM NH4H2PO4缓冲液洗脱的交换柱,在40°C下流速为1.5 mL min(-1)来分离和定量阳离子和阴离子砷物质。在这些条件下,亚砷酸无法与其他砷物质分离,因此需要使用额外的氢化物生成步骤。已测量了当地塔斯马尼亚海带(Durvillea马铃薯),经认证的参考材料(DORM-2)以及一系列市售大型藻类补充剂和寿司海藻中的砷物种浓度,并将其用作内部质量控制样品评估样品制备,提取和测量技术的有效性。

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