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Selective generation of substituted arsines-cryotrapping-atomic absorption spectrometry for arsenic speciation analysis in N-methylglucamine antimonate

机译:N-甲基葡萄糖胺锑酸盐中砷形态分析的取代substituted-冷冻捕集-原子吸收光谱法的选择性生成

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摘要

Hydride generation-cryotrapping-gas chromatography-atomic absorption spectrometry (HG-CT-AAS) was applied for arsenic speciation analysis in an injectable drug, Af-methylglucamine antimonate. The method employs generation of substituted hydrides and selective hydride generation, which makes possible an analysis of arsenites and arsenates and their mono-, di-, and trimethyl substituted species. Interference of the antimony matrix was eliminated using the T-valve to prevent supply of the stibine interferent to the atomizer. The limits of detection in measured sample solutions were 70 ng L~(-1) for inorganic arsenate, 42 ng L~(-1) for mono- and dimethylarsenates and 30 ng L~(-1) for all the other determined species. Concentrations of all methylated species in all samples were below their detection limits. A significant but different amount of inorganic As was found in different batches of the drug: between 0.9 and 2.3 mg L~(-1) with 7% to 10% of the content present as the trivalent form. The accuracy was assessed by the comparison of the determined inorganic arsenic content with the total arsenic content determined by the conventional inductively coupled plasma mass spectrometry. Both methods yielded for individual samples equal values within experimental error. The HG-CT-AAS procedure showed good performance with minimum sample pretreatment at low investment and running costs.
机译:氢化物发生-低温捕集-气相色谱-原子吸收光谱法(HG-CT-AAS)用于可注射药物Af-甲基葡萄糖胺锑酸盐中的砷形态分析。该方法利用了取代氢化物的产生和选择性氢化物的产生,这使得分析砷和砷酸盐及其单,二和三甲基取代物质成为可能。使用T阀消除了锑基质的干扰,以防止向雾化器供应锑代干扰素。在测定的样品溶液中,无机砷酸盐的检出限为70 ng L〜(-1),一氧化二砷和二甲基砷酸盐的检出限为42 ng L〜(-1),所有其他测定物质的检出限为30 ng L〜(-1)。所有样品中所有甲基化物质的浓度均低于其检出限。在不同批次的药物中发现大量但不同的无机As:0.9至2.3 mg L〜(-1),其中三价形式的含量为7%至10%。通过将测定的无机砷含量与通过常规感应耦合等离子体质谱法测定的总砷含量进行比较来评估准确性。两种方法得出的单个样品在实验误差范围内均具有相等的值。 HG-CT-AAS程序具有良好的性能,且样品前处理最少,投资和运行成本低。

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  • 来源
    《Journal of Analytical Atomic Spectrometry》 |2012年第10期|p.1734-1742|共9页
  • 作者单位

    Institute of Analytical Chemistry of the ASCR, v. v. i., Veveri 97, 602 00, Brno, Czech Republic,Instituto de Quimica, Universidade Federal do Rio Grande do Sul, 91501- 970, Porto Alegre, RS, Brazil;

    Institute of Analytical Chemistry of the ASCR, v. v. i., Veveri 97, 602 00, Brno, Czech Republic;

    Institute of Analytical Chemistry of the ASCR, v. v. i., Veveri 97, 602 00, Brno, Czech Republic;

    Departamento de Quimica, Universidade Federal de Santa Maria, 97105- 900, Santa Maria, RS, Brazil,Instituto Nacional de Ciencia e Tecnologia Bioanalitica, Campinas, SP, Brazil;

    Institute of Analytical Chemistry of the ASCR, v. v. i., Veveri 97, 602 00, Brno, Czech Republic;

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