Enzyme-polyelectrolyte multilayer assemblies on reduced graphene oxide field-effect transistors for biosensing applications

被引:123
作者
Piecinini, Esteban [1 ]
Bliem, Christina [2 ]
Reiner-Rozman, Ciril [3 ]
Battaglini, Fernando [4 ]
Azzaroni, Omar [1 ]
Knoll, Wolfgang [3 ]
机构
[1] Univ Nacl La Plata, CONICET, Fac Ciencias Exactas, Inst Invest Fisicoquim Teor & Aplicadas INIFTA,De, Suc 4,CC 16, La Plata, Buenos Aires, Argentina
[2] CEST, Viktor Kaplan Str 2, A-2700 Wiener Neustadt, Austria
[3] Austrian Inst Technol, Donau City Str 1, A-1220 Vienna, Austria
[4] Univ Buenos Aires, Fac Ciencias Exactas & Nat, INQUIMAE, Dept Quim Inorgan Analit & Quim Fis, Ciudad Univ, Buenos Aires, DF, Argentina
关键词
Graphene; Field-effect transistors; Chemical sensors; Biosensors; UREA; PH; IMMOBILIZATION; GLUCOSE; FILMS; ARRAY;
D O I
10.1016/j.bios.2016.10.035
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
We present the construction of layer-by-layer (LbL) assemblies of polyethylenimine and urease onto reduced-graphene-oxide based field-effect transistors (rGO FETs) for the detection of urea. This versatile biosensor platform simultaneously exploits the pH dependency of liquid-gated graphene-based transistors and the change in the local pH produced by the catalyzed hydrolysis of urea. The use of an interdigitated microchannel resulted in transistors displaying low noise, high pH sensitivity (20.3 mu A/pH) and transconductance values up to 800 mu S. The modification of rGO FETs with a weak polyelectrolyte improved the pH response because of its transducing properties by electrostatic gating effects. In the presence of urea, the urease-modified rGO FETs showed a shift in the Dirac point due to the change in the local pH close to the graphene surface. Markedly, these devices operated at very low voltages (less than 500 mV) and were able to monitor urea in the range of 1-1000 mu m, with a limit of detection (LOD) down to 1 mu m, fast response and good long-term stability. The urea-response of the transistors was enhanced by increasing the number of bilayers due to the increment of the enzyme surface coverage onto the channel. Moreover, quantification of the heavy metal Cu2+(with a LOD down to 10 nM) was performed in aqueous solution by taking advantage of the urease specific inhibition.
引用
收藏
页码:661 / 667
页数:7
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