Ge Shenguang, Wu Kaiqing, Zhang Yan, Yan Mei, Yu Jinghua
School of Chemistry and Chemical Engineering, University of Jinan, Jinan 250022, PR China; Shandong Provincial Key Laboratory of Preparation and Measurement of Building Materials, University of Jinan, Jinan 250022, PR China.
School of Chemistry and Chemical Engineering, University of Jinan, Jinan 250022, PR China.
Biosens Bioelectron. 2016 Jun 15;80:215-221. doi: 10.1016/j.bios.2016.01.072. Epub 2016 Jan 29.
A multi-amplified paper-based electrochemical strategy using Pb(2+) dependent DNAzyme as the recognition unit for Pb(2+) detection was developed. In this work, flower-like reduced graphene (FrGO) was prepared utilizing flower-like ZnO as template, which was first one step grown on the gold nanoparticles modified paper working electrode (Au-PWE). After being treated with acid and then modified with Au, a novel sensor platform named Au/FrGO/Au-PWE with large specific surface area and good electrical conductivity was fabricated. The Mn2O3 nanoparticle-assembled hierarchical hollow spheres (H-Mn2O3) was served as nanocarrier to immobilize GOx, HRP and signal strand (S3), resulting to the formation of S3/H-Mn2O3/HRP/GOx bioconjugations. In the presence of Pb(2+), the DNAzyme (S1) was activated and the substrate strand (S2) was cleaved. After the incubation with S3/H-Mn2O3/HRP/GOx in 0.1M HAc-NaAc solution (pH 4.3) containing 30 mM aniline and 15 mM glucose, a readily measurable "turn-on" electrochemical signal could be measured. On the basis of the signal amplification strategy of Au/FrGO/Au-PWE sensing platform and S3/H-Mn2O3/HRP/GOx bioconjugations, the developed biosensor exhibited a good linear response toward over a wide range of concentration from 0.005 to 2000 nM.
开发了一种基于纸基的多放大电化学策略,该策略使用依赖Pb(2+)的DNAzyme作为识别单元来检测Pb(2+)。在这项工作中,以花状ZnO为模板制备了花状还原石墨烯(FrGO),花状ZnO首先在金纳米颗粒修饰的纸工作电极(Au-PWE)上一步生长。经酸处理后再用金修饰,制备了一种具有大比表面积和良好导电性的新型传感器平台Au/FrGO/Au-PWE。将Mn2O3纳米颗粒组装的分级空心球(H-Mn2O3)作为纳米载体固定葡萄糖氧化酶(GOx)、辣根过氧化物酶(HRP)和信号链(S3),形成S3/H-Mn2O3/HRP/GOx生物共轭物。在Pb(2+)存在的情况下,DNAzyme(S1)被激活,底物链(S2)被切割。在含有30 mM苯胺和15 mM葡萄糖的0.1M HAc-NaAc溶液(pH 4.3)中与S3/H-Mn2O3/HRP/GOx孵育后,可以测量到易于测量的“开启”电化学信号。基于Au/FrGO/Au-PWE传感平台和S3/H-Mn2O3/HRP/GOx生物共轭物的信号放大策略,所开发的生物传感器在0.005至2000 nM的宽浓度范围内表现出良好的线性响应。