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基于苝介导的光引发聚合对凝血酶活性进行放大的电化学生物传感器。

An electrochemical biosensor for the amplification of thrombin activity by perylene-mediated photoinitiated polymerization.

机构信息

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

School of Environmental Science, Nanjing XiaoZhuang University, Nanjing, 211171, PR China.

出版信息

Anal Chim Acta. 2024 May 8;1302:342494. doi: 10.1016/j.aca.2024.342494. Epub 2024 Mar 20.

Abstract

BACKGROUND

Thrombin, a coagulation system protease, is a key enzyme involved in the coagulation cascade and has been developed as a marker for coagulation disorders. However, the methods developed in recent years have the disadvantages of complex operation, long reaction time, low specificity and sensitivity. Meanwhile, thrombin is at a lower level in the pre-disease period. Therefore, to accurately diagnose the disease, it is necessary to develop a fast, simple, highly sensitive and specific method using signal amplification technology.

RESULTS

We designed an electrochemical biosensor based on photocatalytic atom transfer radical polymerization (photo-ATRP) signal amplification for the detection of thrombin. Sulfhydryl substrate peptides (without carboxyl groups) are self-assembled to the gold electrode surface via Au-S bond and serve as thrombin recognition probes. The substrate peptide is cleaved in the presence of thrombin to generate -COOH, which can form a carboxylate-Zr(IV)-carboxylate complex via Zr(IV) and initiator (α-bromophenylacetic acid, BPAA). Subsequently, an electrochemical biosensor was prepared by introducing polymer chains with electrochemical signaling molecules (ferrocene, Fc) onto the electrode surface by photocatalytic (perylene, Py) mediated ATRP using ferrocenylmethyl methacrylate (FMMA) as a monomer. The concentration of thrombin was evaluated by the voltammetric signal generated by square wave voltammetry (SWV), and the result showed that the biosensor was linear between 1.0 ng/mL ∼ 10 fg/mL, with a lower detection limit of 4.0 fg/mL (∼0.1 fM). Moreover, it was shown to be highly selective for thrombin activity in complex serum samples and for thrombin inhibition screening.

SIGNIFICANCE

The biosensor is an environmentally friendly and economically efficient strategy while maintaining the advantages of high sensitivity, anti-interference, good stability and simplicity of operation, which has great potential for application in the analysis of complex samples.

摘要

背景

凝血酶是一种凝血系统蛋白酶,是凝血级联反应中的关键酶,已被开发为凝血紊乱的标志物。然而,近年来开发的方法存在操作复杂、反应时间长、特异性和灵敏度低等缺点。同时,在疾病前期,凝血酶的水平较低。因此,为了准确诊断疾病,有必要利用信号放大技术开发一种快速、简单、高灵敏度和特异性的方法。

结果

我们设计了一种基于光催化原子转移自由基聚合(photo-ATRP)信号放大的电化学生物传感器,用于检测凝血酶。巯基底物肽(无羧基)通过 Au-S 键自组装到金电极表面,并作为凝血酶识别探针。存在凝血酶时,底物肽被切割生成 -COOH,-COOH 可通过 Zr(IV)与引发剂(α-溴苯乙酸,BPAA)形成羧酸盐-Zr(IV)-羧酸盐配合物。随后,通过光催化(苝,Py)介导的 ATRP,在电极表面引入带有电化学信号分子(二茂铁,Fc)的聚合物链,以 ferrocenylmethyl methacrylate (FMMA) 为单体,制备电化学生物传感器。通过方波伏安法(SWV)产生的伏安信号评估凝血酶的浓度,结果表明该生物传感器在 1.0ng/mL∼10fg/mL 之间呈线性关系,检测限低至 4.0fg/mL(约 0.1fM)。此外,它在复杂血清样品中对凝血酶活性和凝血酶抑制筛选表现出高度选择性。

意义

该生物传感器是一种环保且经济高效的策略,同时保持了高灵敏度、抗干扰、良好的稳定性和操作简单性的优点,在复杂样品分析中具有很大的应用潜力。

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