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基于 N 掺杂 CQDs@UiO-66/PVA 纳米复合水凝胶的双发射比率荧光探针用于人血浆中哌替啶的定量分析。

Dual-emission ratiometric fluorescent probe based on N-doped CQDs@UiO-66/PVA nanocomposite hydrogel for quantification of pethidine in human plasma.

机构信息

Pharmaceutical Analysis Research Center and Faculty of Pharmacy, Tabriz University of Medical Sciences, Tabriz, Iran.

Student Research Committee, Faculty of Pharmacy, Tabriz University of Medical Sciences, Tabriz, Iran.

出版信息

Mikrochim Acta. 2023 Mar 10;190(4):128. doi: 10.1007/s00604-023-05703-4.

DOI:10.1007/s00604-023-05703-4
PMID:36899094
Abstract

A synchronous fluorescence spectroscopy (SFS) sensor for pethidine detection is described based on UiO-66 metal-organic frameworks (MOFs) modified with N-doped carbon quantum dots (N-CQDs) embedded in hydrogel nanocomposites. Benefitting from the inovative  design of the doping method in the carbonaceous structure, N-CQDs were successfully deposited in the pores of the UiO-66 network. Then, N-CQDs were employed as a sensitive segment toward the target molecules. UiO-66 was used for sensitive and selective sensing of the bonding interactions between N-CQDs and pethidine so that the electron transfer process from UiO-66 to the pethidine-N-CQD complex results in quenching the SFS intensity of UiO-66. To embed the stable and suitable sensing interface for pethidine assessment, the designed nanomaterial was inserted into the hydrogel network. This nanocomposite hydrogel showed two well-resolved emission peaks at 300 nm and 350 nm under ∆λ = 70, which corresponded to N-CQDs and UiO-66, respectively. The SFS sensing platform was employed for ratiometric detection of pethidine with a low limit of detection of 0.002 μg mL over a wide concentration range from 0.005 to 1.0 μg mL. The accurate monitoring of pethidine with a good recovery of 90.8-101.5% indicated their independency from matrix effects for pethidine detection in human plasma being a complicated biological matrix. Scheme 1. General procedure for synthesizing N-CQDs@UiO-66/PVA hydrogel-based nanoprobe and its application for pethidine determination.

摘要

基于 UiO-66 金属-有机骨架(MOFs)修饰的氮掺杂碳量子点(N-CQDs)嵌入水凝胶纳米复合材料,描述了一种用于检测哌替啶的同步荧光光谱(SFS)传感器。受益于碳质结构中掺杂方法的创新设计,N-CQDs 成功沉积在 UiO-66 网络的孔中。然后,N-CQDs 被用作针对目标分子的敏感部分。UiO-66 用于敏感和选择性地感测 N-CQDs 和哌替啶之间的键合相互作用,从而导致从 UiO-66 到哌替啶-N-CQD 配合物的电子转移过程导致 UiO-66 的 SFS 强度猝灭。为了嵌入用于哌替啶评估的稳定且合适的传感界面,设计的纳米材料被插入水凝胶网络中。这种纳米复合水凝胶在 ∆λ=70 下在 300nm 和 350nm 处显示出两个很好分辨的发射峰,分别对应于 N-CQDs 和 UiO-66。SFS 传感平台用于哌替啶的比率检测,检测下限低至 0.002μgmL,浓度范围从 0.005 到 1.0μgmL。在人血浆这一复杂的生物基质中,对哌替啶的准确监测和 90.8-101.5%的良好回收率表明,它们在检测哌替啶时不受基质效应的影响。方案 1. 合成 N-CQDs@UiO-66/PVA 水凝胶基纳米探针的一般程序及其在哌替啶测定中的应用。

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