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基于 MXene 和 ATRP 光催化策略的超灵敏电化学 microRNA-21 检测。

Ultrasensitive electrochemical microRNA-21 detection based on MXene and ATRP photocatalytic strategy.

机构信息

School of Environmental and Biological Engineering, Nanjing University of Science and Technology, 210094, Nanjing, China.

Institute of Advanced Materials (IAM), Nanjing Tech University, 30 South Puzhu Road, 211816, Nanjing, China.

出版信息

Mikrochim Acta. 2024 Jul 19;191(8):472. doi: 10.1007/s00604-024-06542-7.

Abstract

A TiCTMXene-based biosensor has been developed and the photocatalytic atom transfer radical polymerization (photo ATRP) amplification strategy applied to detect target miRNA-21 (tRNA). Initially, TiCTMXene nanosheets were synthesized from the TiAlC MAX precursor via selective aluminum etching. Then, functionalization of TiCTMXene nanosheets with 3-aminopropyl triethoxysilane (APTES) via silylation reactions to facilitate covalent bonding with hairpin DNA biomolecules specifically designed for tRNA detection. Upon binding with the tRNA, the hairpin DNA liberated the azide (N₃) group, initiating a click reaction to affix to the photo ATRP initiator. Through the ATRP photoreaction, facilitated by an organic photoredox catalyst and light, a significant amount of ferrocenyl methyl methacrylate (FMMA) monomer was immobilized on the electrode. Therefore, the electrochemical signal is amplified. The electrochemical efficacy of the biosensor was assessed using square wave voltammetry (SWV). Under optimized conditions, the biosensor demonstrated remarkable sensitivity in detecting tRNA, with a linear detection range from 0.01 fM to 10 pM and a detection limit of 2.81 aM. The findings elucidate that the developed biosensor, in conjunction with the photo ATRP strategy, offers reproducibility, stability, and increased sensitivity, underscoring its potential applications within the experimental medical sector of the biomolecular industry.

摘要

一种基于 TiCTMXene 的生物传感器已经被开发出来,并应用于光催化原子转移自由基聚合(photo ATRP)放大策略来检测靶标 miRNA-21(tRNA)。首先,通过选择性地去除铝元素,从 TiAlC MAX 前体中合成 TiCTMXene 纳米片。然后,通过硅烷化反应将 TiCTMXene 纳米片功能化,使其与专门设计用于检测 tRNA 的发夹 DNA 生物分子进行共价键合。与 tRNA 结合后,发夹 DNA 释放出叠氮化物(N₃)基团,引发点击反应以固定在光 ATRP 引发剂上。通过光 ATRP 光反应,在有机光氧化还原催化剂和光的作用下,大量的二茂铁甲基甲基丙烯酸酯(FMMA)单体被固定在电极上。因此,电化学信号被放大。通过方波伏安法(SWV)评估了生物传感器的电化学功效。在优化条件下,该生物传感器在检测 tRNA 方面表现出显著的灵敏度,线性检测范围为 0.01 fM 至 10 pM,检测限为 2.81 aM。研究结果表明,所开发的生物传感器与 photo ATRP 策略相结合,具有可重复性、稳定性和更高的灵敏度,突出了其在生物分子工业实验医学领域的潜在应用。

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