Key Laboratory of Analytical Chemistry for Biology and Medicine-Ministry of Education, Department of Chemistry, Wuhan University, Wuhan 430072, China.
J Chromatogr A. 2012 Jul 20;1247:49-56. doi: 10.1016/j.chroma.2012.05.059. Epub 2012 May 24.
In this study, a sensitive, selective and reliable analytical method by combining zirconia (ZrO₂) coated stir bar sorptive extraction (SBSE) with large volume sample stacking capillary electrophoresis-indirect ultraviolet (LVSS-CE/indirect UV) was developed for the direct analysis of chemical warfare agent degradation products of alkyl alkylphosphonic acids (AAPAs) (including ethyl methylphosphonic acid (EMPA) and pinacolyl methylphosphonate (PMPA)) and methylphosphonic acid (MPA) in environmental waters. ZrO₂ coated stir bar was prepared by adhering nanometer-sized ZrO₂ particles onto the surface of stir bar with commercial PDMS sol as adhesion agent. Due to the high affinity of ZrO₂ to the electronegative phosphonate group, ZrO₂ coated stir bars could selectively extract the strongly polar AAPAs and MPA. After systematically optimizing the extraction conditions of ZrO₂-SBSE, the analytical performance of ZrO₂-SBSE-CE/indirect UV and ZrO₂-SBSE-LVSS-CE/indirect UV was assessed. The limits of detection (LODs, at a signal-to-noise ratio of 3) obtained by ZrO₂-SBSE-CE/indirect UV were 13.4-15.9 μg/L for PMPA, EMPA and MPA. The relative standard deviations (RSDs, n=7, c=200 μg/L) of the corrected peak area for the target analytes were in the range of 6.4-8.8%. Enhancement factors (EFs) in terms of LODs were found to be from 112- to 145-fold. By combining ZrO₂ coating SBSE with LVSS as a dual preconcentration strategy, the EFs were magnified up to 1583-fold, and the LODs of ZrO₂-SBSE-LVSS-CE/indirect UV were 1.4, 1.2 and 3.1 μg/L for PMPA, EMPA, and MPA, respectively. The RSDs (n=7, c=20 μg/L) were found to be in the range of 9.0-11.8%. The developed ZrO₂-SBSE-LVSS-CE/indirect UV method has been successfully applied to the analysis of PMPA, EMPA, and MPA in different environmental water samples, and the recoveries for the spiked water samples were found to be in the range of 93.8-105.3%.
在这项研究中,我们开发了一种灵敏、选择性和可靠的分析方法,将氧化锆(ZrO₂)涂层搅拌棒吸附萃取(SBSE)与大体积样品堆积毛细管电泳-间接紫外(LVSS-CE/间接 UV)相结合,直接分析烷基膦酸酯(AAPAs)(包括乙基甲基膦酸(EMPA)和频哪基甲基膦酸(PMPA))和甲基膦酸(MPA)在环境水样中的化学战剂降解产物。ZrO₂ 涂层搅拌棒是通过将纳米级 ZrO₂ 颗粒粘附在商用 PDMS 溶胶上制备的。由于 ZrO₂ 对电负性膦酸基团的高亲和力,ZrO₂ 涂层搅拌棒可以选择性地提取强极性 AAPAs 和 MPA。在系统优化 ZrO₂-SBSE 的萃取条件后,评估了 ZrO₂-SBSE-CE/间接 UV 和 ZrO₂-SBSE-LVSS-CE/间接 UV 的分析性能。ZrO₂-SBSE-CE/间接 UV 的检测限(LOD,信噪比为 3)为 13.4-15.9 μg/L,用于 PMPA、EMPA 和 MPA。目标分析物校正峰面积的相对标准偏差(RSD,n=7,c=200 μg/L)在 6.4-8.8%范围内。LOD 时的增强因子(EF)发现为 112-145 倍。通过将 ZrO₂ 涂层 SBSE 与 LVSS 结合作为双重预浓缩策略,EF 放大至 1583 倍,ZrO₂-SBSE-LVSS-CE/间接 UV 的检测限(LOD)分别为 PMPA、EMPA 和 MPA 的 1.4、1.2 和 3.1 μg/L。RSD(n=7,c=20 μg/L)在 9.0-11.8%范围内。所开发的 ZrO₂-SBSE-LVSS-CE/间接 UV 方法已成功应用于不同环境水样中 PMPA、EMPA 和 MPA 的分析,加标水样的回收率在 93.8-105.3%范围内。