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一种基于金纳米粒子/聚邻苯二胺/普鲁士蓝修饰的丝网印刷碳电极的高灵敏安培型葡萄糖生物传感器。

A highly sensitive flow injection amperometric glucose biosensor using a gold nanoparticles/polytyramine/Prussian blue modified screen-printed carbon electrode.

机构信息

Center of Excellence for Trace Analysis and Biosensor, Prince of Songkla University, Hat Yai, Songkhla 90112, Thailand; Division of Physical Science, Faculty of Science, Prince of Songkla University, Hat Yai, Songkhla 90112, Thailand; Center of Excellence for Innovation in Chemistry, Faculty of Science, Prince of Songkla University, Hat Yai, Songkhla 90112, Thailand.

Center of Excellence for Trace Analysis and Biosensor, Prince of Songkla University, Hat Yai, Songkhla 90112, Thailand; Division of Physical Science, Faculty of Science, Prince of Songkla University, Hat Yai, Songkhla 90112, Thailand; Center of Excellence for Innovation in Chemistry, Faculty of Science, Prince of Songkla University, Hat Yai, Songkhla 90112, Thailand.

出版信息

Bioelectrochemistry. 2021 Apr;138:107718. doi: 10.1016/j.bioelechem.2020.107718. Epub 2020 Dec 3.

Abstract

A novel oxidase enzyme sensor was fabricated based on the chemisorption of highly active glucose oxidase (GOx) on gold nanoparticles that were adsorbed on a polytyramine layer (AuNPs/Pty). The GOx/AuNPs/Pty assembly was coated on a Prussian blue (PB)-modified screen-printed carbon electrode (SPCE) to produce the GOx/AuNPs/Pty/PB/SPCE biosensor. The amperometric glucose biosensor response was measured at -0.10 V using a Ag pseudo-reference electrode through the reduction current of the PB mediator in a flow injection analysis system. Under optimised experimental conditions, the developed biosensor displayed linearity over the 1.0 μM-1.0 mM glucose concentration range and a limit of detection of 1.0 μM (S/N ≥ 3). A low value for the Michaelis constant of 0.21 mM indicated that the immobilised GOx had high affinity for glucose. The developed biosensor exhibited excellent operational stability over 374 injections, long-term stability over 3 weeks, good reproducibility (relative standard deviations = 1.9%-4.3%) and high selectivity. The results obtained analysing glucose in blood plasma samples were satisfactory when compared with the corresponding results recorded implementing the standard hexokinase-spectrophotometric method (P > 0.05).

摘要

一种新型的氧化酶传感器是基于高度活性的葡萄糖氧化酶(GOx)在吸附在聚酪氨酸层(AuNPs/Pty)上的金纳米粒子上的化学吸附而构建的。GOx/AuNPs/Pty 组装体涂覆在普鲁士蓝(PB)修饰的丝网印刷碳电极(SPCE)上,以产生 GOx/AuNPs/Pty/PB/SPCE 生物传感器。通过在流动注射分析系统中 PB 介体的还原电流,使用 Ag 伪参比电极在-0.10 V 下测量安培葡萄糖生物传感器响应。在优化的实验条件下,开发的生物传感器在 1.0 μM-1.0 mM 葡萄糖浓度范围内显示出线性,检测限为 1.0 μM(S/N ≥ 3)。米氏常数的低值 0.21 mM 表明固定化 GOx 对葡萄糖具有高亲和力。该生物传感器在 374 次注射中表现出出色的操作稳定性,在 3 周的长期稳定性,良好的重现性(相对标准偏差 = 1.9%-4.3%)和高选择性。与实施标准己糖激酶分光光度法记录的相应结果相比,分析血浆样品中葡萄糖的结果令人满意(P > 0.05)。

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