Au/NiFe2O4 nanoparticle-decorated graphene oxide nanosheets for electrochemical immunosensing of amyloid beta peptide

被引:44
作者
Devi, Rashmita [1 ,2 ]
Gogoi, Satyabrat [1 ]
Dutta, Hemant Sankar [1 ,2 ]
Bordoloi, Manabjyoti [2 ,3 ]
Sanghi, Sunil K. [4 ]
Khan, Raju [4 ]
机构
[1] NEIST, CSIR, Analyt Chem Grp, Mat Sci & Technol Div, Jorhat 785006, Assam, India
[2] Acad Sci & Innovat Res AcSIR, CSIR NEIST Campus, Jorhat, Assam, India
[3] CSIR NEIST, Chem Sci & Technol Div, Nat Prod Chem Grp, Jorhat 785006, Assam, India
[4] CSIR AMPRI, Microfluid & MEMS Ctr, Bhopal 462026, MP, India
来源
NANOSCALE ADVANCES | 2020年 / 2卷 / 01期
关键词
SURFACE-PLASMON RESONANCE; NANOCOMPOSITE;
D O I
10.1039/c9na00578a
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
In the present work, an electrochemical immunosensor has been fabricated for the detection of amyloid beta peptide (beta A(1--42)) based on a gold nanoparticle/nickel ferrite decorated graphene oxide-chitosan nanocomposite (Au/NiFe2O4@GO-Ch) modified glassy carbon electrode (GCE) as an effective sensing platform. beta A(1-42) has been analyzed as a potential biomarker for its application in Alzheimer's disease monitoring. The combination of highly conducting Au and NiFe2O4 nanoparticles on two-dimensional GO nanosheets provides an excellent platform for sensitive and selective sensing applications. A miniaturized Au/NiFe2O4@GO-Ch/GCE immunosensor was prepared by immobilization of beta A antibody onto Au//NiFe2O4@GO-Ch/GCE via carbodiimide coupling. Various characterization techniques were utilized in the study to estimate the morphological and electronic attributes of the components used to fabricate the immunosensor. Differential pulse voltammetry (DPV) was performed to study the amperometric response of the developed immunosensor as a function of beta A(1-42) concentration. The DPV results confirmed that the immunosensor detected beta A(1-42) selectively and demonstrated a wide linear range from 1 pg mL(-1) to 1 ng mL(-1) and a detection limit of 3.0 pg mL(-1). Furthermore, the immunosensor also indicated its clinical viability by detecting beta A(1-42) in cerebrospinal fluid.
引用
收藏
页码:239 / 248
页数:10
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