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源自蛋壳的绿色氮硫共掺杂碳点作为用于甲硝唑非侵入式检测的高性能适配体传感界面。

Green nitrogen and sulfur co-doped carbon dots derived from eggshell as a high performance aptasensing interface for non-invasive detection of metronidazole.

作者信息

Ghiasi Maryam, Ghanbarzadeh Mahsa, Ghaffarinejad Ali, Shahdost-Fard Faezeh

机构信息

Research Laboratory of Real Samples Analysis, Faculty of Chemistry, Iran University of Science and Technology (IUST), Tehran, 1684613114, Iran.

Research Laboratory of Real Samples Analysis, Faculty of Chemistry, Iran University of Science and Technology (IUST), Tehran, 1684613114, Iran; Electroanalytical Chemistry Research Center, Iran University of Science and Technology (IUST), Tehran, 1684613114, Iran.

出版信息

Talanta. 2025 Apr 1;285:127363. doi: 10.1016/j.talanta.2024.127363. Epub 2024 Dec 11.

Abstract

BACKGROUND

The concentration monitoring of the banned metronidazole (MTZ) drug as the alarmed carcinogenic agent in human biofluids is medically essential. The electrochemical aptasensors are good candidates to overcome some presence challenges in the detection process.

RESULTS

Herein, an electrochemical aptasensor based on nitrogen and sulfur co-doped carbon dots (NcS-CDs) has been developed for the high-sensitive detection of MTZ for the first time. The N-S-CDs have been synthesized from eggshell waste and the aptasensing interface has been fabricated by the attachment of the N-S-CDs to the glassy carbon electrode surface to fix the high-density aptamer (Apt) sequences via silver nanocubes (AgNCs). The electrochemical signal of the redox probe has changed by trapping the MTZ on the Apt's arm onto the aptasensing interface. The molecular dynamic simulation visually confirmed how the Apt binds to the MTZ. The resulting aptasensor measured MTZ in a wide linear range value from 1 fM to 901.4 nM with a limit of detection value of 333.3 aM and high selectivity regarding some possible interferences.

SIGNIFICANCE

The results reveal that the novel aptasensor has high potential applicability for the non-invasive monitoring of MTZ in human saliva and urine, and also, the tap water analysis. Utilizing waste-derived nanomaterials for the aptasensor fabrication not only less the fabrication costs but also guarantees the greenness of the applied methodology according to sustainable chemistry principles as evaluated by two international index metrics.

摘要

背景

对作为人类生物流体中警示致癌物的禁用甲硝唑(MTZ)药物进行浓度监测在医学上至关重要。电化学适体传感器是克服检测过程中一些现有挑战的良好选择。

结果

在此,首次开发了一种基于氮硫共掺杂碳点(NcS-CDs)的电化学适体传感器,用于高灵敏度检测MTZ。N-S-CDs由蛋壳废料合成,通过将N-S-CDs附着在玻碳电极表面来构建适体传感界面,以通过银纳米立方体(AgNCs)固定高密度适体(Apt)序列。氧化还原探针的电化学信号通过将MTZ捕获在适体臂上并传递到适体传感界面而发生变化。分子动力学模拟直观地证实了适体如何与MTZ结合。所得适体传感器在1 fM至901.4 nM的宽线性范围内测量MTZ,检测限为333.3 aM,对一些可能的干扰具有高选择性。

意义

结果表明,这种新型适体传感器在无创监测人唾液和尿液中的MTZ以及自来水分析方面具有很高的潜在适用性。利用废弃物衍生的纳米材料制造适体传感器,不仅降低了制造成本,还根据可持续化学原理,通过两个国际指标衡量标准确保了所应用方法的绿色性。

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