适配体亲和柱萃取-免疫层析条带法检测镉(II)

IF 2.8 3区 工程技术 Q2 CHEMISTRY, ANALYTICAL
Peng Li, Jiawei Shi, Cong Ji, Changrui Xing, Yong Fang
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引用次数: 0

摘要

饮用水中镉(II) (Cd(II))的存在是一个重大问题。而免疫层析条对微量Cd(II)缺乏敏感性,易受共存离子的影响。本研究建立了Cd-aptamer亲和柱(Cd- aac),用于提取Cd(II)。富集的Cd(II)用乙二胺四乙酸洗脱,随后用免疫层析条快速定量。研究了Cd-AAC的制备、固相萃取条件、干扰离子的影响以及色谱柱的重复使用。在最佳条件下,预浓缩10 mL水样,Cd(II)的检出限为0.1µg/L,增强系数为10。该方法在0.3µg/L和1.0µg/L浓度下,批内测量的精密度(相对标准偏差n = 6)分别为3.1%和1.6%,批间测量的精密度分别为4.4%和2.3%。将该方法应用于水样中Cd(II)的测定,所得结果与电感耦合等离子体质谱分析结果一致。该方法直接、快速、经济、灵敏。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Aptamer Affinity Column Extraction Coupled With Immunochromatographic Strip for the Detection of Cadmium(II)

The presence of cadmium(II) (Cd(II)) in drinking water is a significant concern. While immunochromatographic strips often lack sensitivity for trace Cd(II) and are easily affected by coexisting ions. In this study, a specific Cd-aptamer affinity column (Cd-AAC) was developed for the extraction of Cd(II). The enriched Cd(II) was eluted using ethylenediaminetetraacetic acid and subsequently quantified rapidly with immunochromatographic strips. The preparation of the Cd-AAC, conditions of solid-phase extraction, the effects of interfering ions, and the reusability of the column were thoroughly investigated. Under optimal conditions, preconcentrating 10 mL of water samples achieved a limit of detection of 0.1 µg/L for Cd(II), with an enhancement factor of 10. The precision of the method (relative standard deviation, n = 6) was 3.1% and 1.6% for intra-batch, and 4.4% and 2.3% for inter-batch measurements of Cd(II) at 0.3 and 1.0 µg/L, respectively. The method was applied to the determination of Cd(II) in water samples, yielding results consistent with inductively coupled plasma mass spectrometry analysis. This approach is straightforward, rapid, economical, and sensitive.

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来源期刊
Journal of separation science
Journal of separation science 化学-分析化学
CiteScore
6.30
自引率
16.10%
发文量
408
审稿时长
1.8 months
期刊介绍: The Journal of Separation Science (JSS) is the most comprehensive source in separation science, since it covers all areas of chromatographic and electrophoretic separation methods in theory and practice, both in the analytical and in the preparative mode, solid phase extraction, sample preparation, and related techniques. Manuscripts on methodological or instrumental developments, including detection aspects, in particular mass spectrometry, as well as on innovative applications will also be published. Manuscripts on hyphenation, automation, and miniaturization are particularly welcome. Pre- and post-separation facets of a total analysis may be covered as well as the underlying logic of the development or application of a method.
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