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用于超痕量铍检测的高选择性分子印迹电化学发光传感器。

A highly selective molecularly imprinted electrochemiluminescence sensor for ultra-trace beryllium detection.

机构信息

Guangxi Key Laboratory of Electrochemical and Magnetochemical Function Materials, College of Chemistry and Bioengineering, Guilin University of Technology, Guilin 541004, PR China.

Guangxi Key Laboratory of Electrochemical and Magnetochemical Function Materials, College of Chemistry and Bioengineering, Guilin University of Technology, Guilin 541004, PR China.

出版信息

Anal Chim Acta. 2015 Apr 29;871:51-6. doi: 10.1016/j.aca.2015.02.038. Epub 2015 Feb 16.

Abstract

A new molecularly imprinted electrochemiluminescence (ECL) sensor was proposed for highly sensitive and selective determination of ultratrace Be(2+) determination. The complex of Be(2+) with 4-(2-pyridylazo)-resorcinol (PAR) was chosen as the template molecule for the molecularly imprinted polymer (MIP). In this assay, the complex molecule could be eluted from the MIP, and the cavities formed could then selectively recognize the complex molecules. The cavities formed could also work as the tunnel for the transfer of probe molecules to produce sound responsive signal. The determination was based on the intensity of the signal, which was proportional to the concentrations of the complex molecule in the sample solution, and the Be(2+) concentration could then be determined indirectly. The results showed that in the range of 7×10(-11 )mol L(-1) to 8.0×10(-9) mol L(-1), the ECL intensity had a linear relationship with the Be(2+) concentrations, with the limit of detection of 2.35×10(-11) mol L(-1). This method was successfully used to detect Be(2+) in real water samples.

摘要

一种新型的分子印迹电化学发光(ECL)传感器被提出,用于痕量铍(Ⅱ)的高灵敏和选择性测定。将铍(Ⅱ)与 4-(2-吡啶偶氮)-间苯二酚(PAR)的配合物选作分子印迹聚合物(MIP)的模板分子。在该测定中,配合物分子可以从 MIP 中洗脱出来,而形成的空穴可以选择性地识别配合物分子。形成的空穴也可以作为探针分子转移的通道,产生声音响应信号。测定基于信号强度,该信号强度与样品溶液中配合物分子的浓度成正比,然后可以间接测定铍(Ⅱ)的浓度。结果表明,在 7×10(-11 )mol L(-1)至 8.0×10(-9) mol L(-1)范围内,ECL 强度与铍(Ⅱ)浓度呈线性关系,检出限为 2.35×10(-11) mol L(-1)。该方法成功地用于实际水样中铍(Ⅱ)的检测。

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