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基于 FeO@MIP 纳米催化探针的新型 SERS 定量分析超痕量氯霉素的策略。

A new SERS quantitative analysis strategy for ultratrace chloramphenicol with FeO@MIP nanocatalytic probe.

机构信息

Key Laboratory of Ecology of Rare and Endangered Species and Environmental Protection (Guangxi Normal University), Ministry of Education, Guilin 541004, China; Guangxi Key Laboratory of Environmental Pollution Control Theory and Technology, Guilin 541004, China; Guangxi Key Laboratory of Environmental Processes and Remediation in Ecologically Fragile Regions, China.

Key Laboratory of Ecology of Rare and Endangered Species and Environmental Protection (Guangxi Normal University), Ministry of Education, Guilin 541004, China; Guangxi Key Laboratory of Environmental Pollution Control Theory and Technology, Guilin 541004, China; Guangxi Key Laboratory of Environmental Processes and Remediation in Ecologically Fragile Regions, China.

出版信息

Spectrochim Acta A Mol Biomol Spectrosc. 2024 Dec 5;322:124732. doi: 10.1016/j.saa.2024.124732. Epub 2024 Jun 25.

Abstract

Three functional magnetic nanocatalytic probe, which integrates recognition, catalytic amplification, and separation enrichment, is a new approach to construct a simple, fast, highly selective, and sensitive analytical method. In this article, a new magnetic nanosurface molecularly imprinted polymer nanoprobe (FeO@MIP) with trifunctionality was rapidly prepared using a microwave-assisted method with magnetic FeO nanoparticles as a substrate, chloramphenicol (CAP) as a template molecule, and methacrylic acid as a functional monomer. The characterized nanoprobe was found that could specifically recognize CAP, strongly catalyze the new indicator nanoreaction of fructose (DF)-HAuCl. The gold nanoparticles (AuNPs) exhibit strong resonance Rayleigh scattering (RRS) and surface enhanced Raman scattering (SERS) effects. Upon addition of CAP, the SERS/RRS signals were linearly weakened. Accordingly, a new SERS/RRS analysis platform for highly sensitive and selective determination of CAP was constructed. The SERS linear range was 0.0125-0.1 nmol/L, with detection limit (DL) of 0.004 nmol/L CAP. Furthermore, it could be combined with magnet-enriched separation to further improve the sensitivity, with a DL of 0.04 pmol/L CAP. The SERS method has been used for the determination of CAP in real samples, with relative standard deviations of 2.37-9.89 % and the recovery of 95.24-107.1 %.

摘要

三种功能磁共振纳米催化探针,集识别、催化放大和分离富集于一体,是构建简单、快速、高选择性、高灵敏度分析方法的新方法。本文采用微波辅助法,以磁性 FeO 纳米粒子为基质,氯霉素(CAP)为模板分子,甲基丙烯酸为功能单体,快速制备了一种新型磁性纳米表面分子印迹聚合物纳米探针(FeO@MIP)。该探针具有三重功能,能够特异性识别 CAP,并强烈催化新的果糖(DF)-HAuCl 指示剂纳米反应。金纳米粒子(AuNPs)表现出强烈的共振瑞利散射(RRS)和表面增强拉曼散射(SERS)效应。加入 CAP 后,SERS/RRS 信号线性减弱。因此,构建了一种用于高灵敏度和选择性测定 CAP 的新 SERS/RRS 分析平台。SERS 的线性范围为 0.0125-0.1 nmol/L,检测限(DL)为 0.004 nmol/L CAP。此外,它可以与磁富集分离结合使用,进一步提高灵敏度,检测限为 0.04 pmol/L CAP。该 SERS 方法已用于实际样品中 CAP 的测定,相对标准偏差为 2.37-9.89%,回收率为 95.24-107.1%。

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