...
首页> 外文期刊>Analytical and bioanalytical chemistry >Label-free electrochemical immunosensor for ultrasensitive detection of neuron-specific enolase based on enzyme-free catalytic amplification
【24h】

Label-free electrochemical immunosensor for ultrasensitive detection of neuron-specific enolase based on enzyme-free catalytic amplification

机译:基于酶催化扩增的无抗敏检测无敏感检测的无标记电化学免疫传感器

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

Abstract Enzyme-free catalytic amplification is of great significance for sensitive label-free electrochemical immunosensors. In this study, an enzyme-free catalytic amplification based label-free amperometric immunosensor was developed for sensitive detection of neuron-specific enolase (NSE) by use of a AuPd nanoparticle–multiwalled carbon nanotube (AuPd-MWCNT) composite, ferrocenecarboxaldehyde (Fc-CHO), and chitosan hybrid hydrogel. The intrinsic virtues of chitosan not only resulted in bioactivity of the attached antibodies and made the other component of the immunosensor easier to fix on the electrode, but also imparted abundant binding sites to the hydrogel to condense Fc-CHO to achieve the initial signal amplification. Fc-CHO, which served as an electroactive species to generate a redox response, also exhibits excellent electrocatalytic activity toward H~(2)O~(2). AuPd-MWCNT composite, with enhanced peroxidase-like catalytic activity, could catalyze H~(2)O~(2)to accelerate electron transfer. When H~(2)O~(2)was present in the detection solution, synergetic catalysis of Fc-CHO and AuPd-MWCNT composite toward H~(2)O~(2)was achieved, thus realizing enzyme-free signal amplification. On the basis of this enzyme-free signal amplification, the electrochemical immunosensing platform provided a wide linear range from 1 pg mL_(-1)to 100 ng mL_(-1), a low detection limit of 0.483 pg mL_(-1), and high sensitivity of 7.22 μA (log~(10) C ~(NSE))_(-1). Moreover, the immunosensor showed enormous potential in clinical application. Graphical abstract An enzyme-free catalytic amplification based label-free amperometric immunosensor was developed for sensitive detection of neuron-specific enolase (NSE) by use of a AuPd nanoparticle–multiwalled carbon nanotube (MWCNT) composite, ferrocenecarboxaldehyde (Fc-CHO), and chitosan (CS) hybrid hydrogel. BSA bovine serum albumin, GA glutaraldehyde, SWV square wave voltammetry
机译:摘要无酶催化扩增对于无敏感的无标签电化学免疫调菌体具有重要意义。在该研究中,通过使用AUPD纳米颗粒 - 多壁碳纳米管(AUPD-MWCNT)复合物,FerrocenCarboxaldehyde(FC- CHO)和壳聚糖杂交水凝胶。壳聚糖的内在优点不仅导致附着抗体的生物活性,并使免疫传感器的其他组分更容易固定在电极上,而且还赋予水凝胶的丰富的结合位点以冷凝Fc-Cho以实现初始信号放大。用作产生氧化还原响应的电活性物质的FC-CHO也表现出优异的电催化活性,朝向H〜(2)O〜(2)。 AUPD-MWCNT复合材料,具有增强的过氧化物酶样催化活性,可催化H〜(2)O〜(2)加速电子转移。当H〜(2)O〜(2)存在于检测溶液中,实现了Fc-Cho和Aupd-MWCNT复合材料的协同催化,从而实现了无酶信号放大。在这种无酶的信号放大的基础上,电化学免疫抑制平台提供宽的线性范围从1pg ml _( - 1)至100ng ml _( - 1),低检测限为0.483pg ml _( - 1),高灵敏度为7.22μA(log〜(10)c〜(nse))_( - 1)。此外,免疫传感器在临床应用中表现出巨大的潜力。图解摘要通过使用AUPD纳米粒子 - 多壁碳纳米管(MWCNT)复合物,铁核羧酸甲醛(FC-CHO),开发了一种无酶无催化扩增的基于无标记的无量动性免疫传感器,用于通过使用AUPD纳米粒子 - 多晶的碳纳米管(MWCNT)复合物,铁核羧甲醛(FC-CHO)和壳聚糖(CS)杂交水凝胶。 BSA牛血清白蛋白,GA戊二醛,SWV方波伏安

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号