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采用强阴离子交换盘的固相萃取与瓶内固相衍生化组合,用于测定神经毒剂标志物。

Combination of solid phase extraction and in vial solid phase derivatization using a strong anion exchange disk for the determination of nerve agent markers.

机构信息

Swedish Defence Research Agency, FOI CBRN Defence and Security, SE-901 82 Umeå, Sweden.

出版信息

J Chromatogr A. 2009 Nov 27;1216(48):8452-9. doi: 10.1016/j.chroma.2009.10.017. Epub 2009 Oct 12.

Abstract

Alkylphosphonic acids (APAs) are degradation products and chemical markers of organophosphorous (OP) nerve agents (chemical warfare agents). Anion exchange disk-based solid phase extraction (SPE) has been combined with in vial solid phase derivatization (SPD) and GC-MS analysis for the determination of APAs in aqueous samples. The optimization of critical method parameters, such as the SPD reaction, was achieved using statistical experimental design and multivariate data analysis. The optimized method achieved quantitative recoveries in the range from 83% to 101% (n=13, RSD from 4% to 10%). The method was sensitive, with LODs in SIM mode of 0.14 ppb, and demonstrated excellent linearity with an average R(2)>or=0.99 over the concentration range of 0.07-1.4 ppm in full scan mode and from 0.14 ppb to 14 ppb in SIM mode. For forensic applications, aqueous samples containing APAs at concentrations exceeding 14 ppb were concentrated and target analytes were successfully identified by spectral library and retention index matching. Method robustness was evaluated using aqueous samples from the official OPCW Proficiency Test (round 19) and all APAs present in the sample were conclusively identified. The SPE disk retained the underivatized APAs in a stable condition for extended periods of time. No significant losses of APAs from the disk were observed over a 36-day period. Overall, the method is well suited to the qualitative and quantitative analysis of degradation markers of OP nerve agents in aqueous matrices with simplicity, a low risk of cross-contamination and trace level sensitivity.

摘要

烷基膦酸(APAs)是有机磷(OP)神经毒剂(化学战剂)的降解产物和化学标志物。基于阴离子交换盘的固相萃取(SPE)与瓶内固相衍生化(SPD)和 GC-MS 分析相结合,用于测定水样中的 APAs。通过统计实验设计和多元数据分析,对 SPD 反应等关键方法参数进行了优化。该优化方法在 83%至 101%(n=13,RSD 为 4%至 10%)的范围内实现了定量回收。该方法具有较高的灵敏度,SIM 模式下的 LODs 为 0.14 ppb,在全扫描模式下浓度范围为 0.07-1.4 ppm 时平均 R(2)>or=0.99,在 SIM 模式下浓度范围为 0.14 ppb 至 14 ppb 时平均 R(2)>or=0.99,具有良好的线性关系。对于法医应用,将浓度超过 14 ppb 的含有 APAs 的水样进行浓缩,通过光谱库和保留指数匹配成功地鉴定了目标分析物。使用官方 OPCW 能力验证(第 19 轮)水样评估方法的稳健性,并且成功鉴定了样品中存在的所有 APAs。SPE 盘在很长一段时间内以稳定的状态保留未衍生的 APAs。在 36 天的时间内,未观察到 APAs 从磁盘上明显损失。总的来说,该方法具有简单、交叉污染风险低和痕量灵敏度高等特点,非常适合于定性和定量分析水样中 OP 神经毒剂的降解标志物。

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