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通过掺杂碳点的分子印迹聚合物对牛奶中青霉素 G 钠的选择性吸附和识别。

Selective adsorption and identification of penicillin G sodium in milk by molecularly imprinted polymer doped carbon dot.

机构信息

School of Chemistry and Chemical Engineering, Key Laboratory for Chemical Engineering and Technology, State Ethnic Affairs Commission, North Minzu University, Yinchuan, 750021, China.

CAS Key Laboratory of Separation Science for Analytical Chemistry, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian, 116023, China.

出版信息

Mikrochim Acta. 2024 Mar 7;191(4):186. doi: 10.1007/s00604-024-06269-5.

Abstract

A carbon dot (CD) was prepared by o-phenylenediamine and water, which showed bright yellow fluorescence under ultraviolet light irradiation (λ = 580 nm), and verified good fluorescence quenching effect on penicillin G sodium (Png-Na). Using methacrylic acid as a functional monomer, ethylene glycol dimethacrylate as a crosslinker, and Png-Na as a template, a kind of composite microsphere combining CD and molecularly imprinted polymer (MIP) was synthesized by surface-initiated atomic transfer radical polymerization (SI-ATRP). For reasons of comparison, we also prepared MIP without CD and non-imprinted polymers (NIPs). Through static and dynamic adsorption experiments, the maximum adsorption capacity was 47.05 mg g and the equilibrium time was 30 min. High-performance liquid chromatography (HPLC) was utilized to determine the content of Png-Na in the spiked milk samples. A sensitive, rapid, and simple method for determination of Png-Na in food samples was developed. The utilized approach enabled the quantification of Png-Na within the concentration range 20-1000 μg L (with a limit of detection of 5 μg L). The recoveries achieved were in the range 93.3-98.2%, with a relative standard deviation of 1.2-4.2%. The results demonstrated that CD@MIP possessed the capability of specific adsorption and fluorescence detection of Png-Na, enabling simultaneous detection and enrichment of Png-Na in real samples.

摘要

一种碳点(CD)是由邻苯二胺和水制备的,在紫外光照射下(λ=580nm)呈现出亮黄色荧光,并验证了对青霉素 G 钠(Png-Na)有良好的荧光猝灭效果。以甲基丙烯酸为功能单体,乙二醇二甲基丙烯酸酯为交联剂,以 Png-Na 为模板,通过表面引发原子转移自由基聚合(SI-ATRP)合成了一种结合 CD 和分子印迹聚合物(MIP)的复合微球。出于比较的原因,我们还制备了没有 CD 的 MIP 和非印迹聚合物(NIPs)。通过静态和动态吸附实验,最大吸附容量为 47.05mg/g,平衡时间为 30min。高效液相色谱(HPLC)用于测定牛奶样品中 Png-Na 的含量。开发了一种用于测定食品样品中 Png-Na 的灵敏、快速和简单的方法。该方法可用于定量测定 Png-Na 的浓度范围为 20-1000μg/L(检出限为 5μg/L)。回收率在 93.3-98.2%之间,相对标准偏差为 1.2-4.2%。结果表明,CD@MIP 具有对 Png-Na 的特异性吸附和荧光检测能力,能够实现实际样品中 Png-Na 的同时检测和富集。

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