首页> 外文期刊>Sensors and Actuators >Nanoarchitectures based on multi-walled carbon nanotubes non-covalently functionalized with Concanavalin A: A new building-block with supramolecular recognition properties for the development of electrochemical biosensors
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Nanoarchitectures based on multi-walled carbon nanotubes non-covalently functionalized with Concanavalin A: A new building-block with supramolecular recognition properties for the development of electrochemical biosensors

机译:基于多壁碳纳米管的纳米体系结构与康丹林A的非共价官能化:一种新的电化学生物传感器发展超分子识别性能的新构建块

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We propose an innovative nanoarchitecture for the development of electrochemical biosensors based on the non-covalent functionalization of multi-walled carbon nanotubes (MWCNTs) with the lectin Concanavalin A (ConA) and the site-specific supramolecular binding of glycobiomolecules. As proof-of-concept, we propose the use of two glycoenzymes, glucose oxidase (GOx) and horseradish peroxidase (HRP), for building mono and bienzymatic glucose biosensors. The selected conditions for the preparation of the dispersion were 1.5 mg MWCNTs in 1.0 mL of 2.0 mg mL(-1) ConA sonicated for 5.0 min with sonicator probe. The monoenzymatic glucose biosensor was prepared by casting GCE with the MWCNTs-ConA dispersion (GCE/MWCNTs-ConA) followed by the interaction with GOx (GCE/MWCNTs-ConA/GOx), while the bienzymatic one was obtained by interaction of GCE/ MWCNTs-ConA with GOx + HRP (GCE/MWCNTs-ConA/GOx-HRP). The best analytical performance was obtained with the bienzymatic biosensor from the amperometric response at -0.050 V in the presence of 1.0 x 10(-4) M hydroquinone. The sensitivity was (2.22 +/- 0.03) mu A mM(-1) (which was 5.2 times higher than the one obtained with the monoenzymatic biosensor) and a detection limit of 0.31 mu M. The reproducibility was 5.4% and the biosensor was challenged with human blood serum showing an excellent correlation with the values reported by the laboratory.
机译:我们提出了一种创新的纳米建筑,用于基于多壁碳纳米管(MWCNT)的非共价官能传感器与凝集素康昔林A(Cona)和糖胆碱的特异性超分子结合的基于多壁碳纳米管(MWCNT)的非共价官能化的开发。作为概念证明,我们提出了使用两种甘油酶,葡萄糖氧化酶(GOX)和辣根过氧化物酶(HRP),用于构建单体和酶酶葡萄糖生物传感器。将选定的分散体的条件为1.0ml 2.0mg ml(-1)Cona的1.5mg mwcnts,Songator探针超声处理5.0分钟。通过用MWCNTS-CONA分散(GCE / MWCNTS-CONA)浇注GCE,然后与GOX(GCE / MWCNTS-CONA / GOX)相互作用来制备单次酶葡萄糖生物传感器,而通过GCE / MWCNT的相互作用获得酶酶-CONA使用GOX + HRP(GCE / MWCNTS-CONA / GOX-HRP)。在1.0×10(-4)米甲基醌的存在下,在-0.050V的效果响应中获得最佳分析性能。敏感性是(2.22 +/- 0.03)mm a mm(-1)(比用单酶生物传感器获得的15.2倍),检测限为0.31μm。再现性为5.4%,生物传感器是用人血清挑战,显示出与实验室报道的价值观的优异相关性。

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