An electrodeposited Au nanoparticle/porous graphene nanoribbon composite for electrochemical detection of alpha-fetoprotein

被引:45
作者
Jothi, Lavanya [1 ]
Jaganathan, Saravana Kumar [2 ,3 ,4 ]
Nageswaran, Gomathi [1 ]
机构
[1] Indian Inst Space Sci & Technol, Dept Chem, Thiruvananthapuram 695547, Kerala, India
[2] Ton Duc Thang Univ, Dept Management Sci & Technol Dev, Ho Chi Minh City, Vietnam
[3] Ton Duc Thang Univ, Fac Sci Appl, Ho Chi Minh City, Vietnam
[4] Univ Hull, Dept Engn, Fac Sci & Engn, Kingston Upon Hull HU6 7RX, N Humberside, England
关键词
Porous graphene nanoribbons; Gold nanoparticles; Alpha fetoprotein; Differential pulse voltammetry; SELF-ASSEMBLED MONOLAYERS; POROUS GRAPHENE; AMPEROMETRIC IMMUNOSENSOR; GOLD NANOPARTICLES; BIOSENSORS; SENSORS; OXIDE;
D O I
10.1016/j.matchemphys.2019.122514
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
In this work, a novel label-free electrochemical immunosensor for the detection of alpha-fetoprotein (AFP) is fabricated for early diagnosis and prognostics of liver cancer. A porous graphene nanoribbon (PGNR) was synthesized via chemical reduction method and it was electrodeposited with gold nanoparticles (AuNPs) to obtain AuNPs/PGNR hybrid nanomaterial. Anti-AFP was immobilized onto AuNPs/PGNR/glassy carbon electrode and anti-APP/AuNPs/PGNR/GCE was further studied to demonstrate its electrocatalytic activity towards AFP antigen. PGNR enhances the electroactive surface area and the electron transfer ability between the electrode and redox probe while the AuNPs deposited on PGNR are used to immobilize biomolecules and to facilitate the electron transport. The superior biosensing performance towards AFP under physiological pH condition is demonstrated by a corresponding decreased peak current in differential pulse voltammetry for a wide linear range (5-60 ng/mL) with a low detection limit of 1 ng/mL. Detection of AFP in serum samples by this label-free electrochemical immunosensor without fouling or significant interference implies that the anti-AFP/AuNPs/PGNR modified GCE has a great application potential for clinical diagnosis of AFP.
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页数:7
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