共 27 条
Au-ionic liquid functionalized reduced graphene oxide immunosensing platform for simultaneous electrochemical detection of multiple analytes
被引:100
作者:
Liu, Na
[1
,2
]
Ma, Zhanfang
[2
]
机构:
[1] Capital Normal Univ, Coll Life Sci, Beijing 100048, Peoples R China
[2] Capital Normal Univ, Dept Chem, Beijing 100048, Peoples R China
基金:
中国国家自然科学基金;
北京市自然科学基金;
关键词:
Au nanoparticle;
Ionic liquid functionalized reduced graphene oxide;
Electrochemical immunosensor;
Carcinoembryonic antigen;
Alpha-fetoprotein;
LABEL-FREE IMMUNOSENSOR;
GOLD NANOPARTICLES;
OXYGEN REDUCTION;
TUMOR-MARKERS;
ELECTROCATALYTIC ACTIVITY;
CARCINOEMBRYONIC ANTIGEN;
CARBON NANOTUBES;
NANOCOMPOSITES;
IMMUNOASSAY;
PERFORMANCE;
D O I:
10.1016/j.bios.2013.07.051
中图分类号:
Q6 [生物物理学];
学科分类号:
071011 ;
摘要:
In this work, an Au-ionic liquid functionalized reduced graphene oxide nanocomposite (IL-rGO-Au) was fabricated via the self-assembly of ionic liquid functionalized reduced graphene oxide (IL-rGO) and gold nanoparticles (AuNPs) by electrostatic interaction. The IL-rGO can be synthesized and stabilized by introducing the cations of the amine-terminated ionic liquids (IL-NH2) into the graphene oxide (GO). With the assistance of IL-NH2, AuNPs were uniformly and densely absorbed on the surfaces of the IL-rGO. The proposed IL-rGO-Au nanocomposite can be used as an immunosensing platform because it can not only facilitate the electrons transfer of the electrode surface but also provide a large accessible surface area for the immobilization of abundant antibody. To assess the performance of the IL-rGO-Au nanocomposite, a sandwich-type electrochemical immunosensor was designed for simultaneous multianalyte detection (carcinoembryonic antigen (CEA) and alpha-fetoprotein (AFP) as model analytes). The chitosan (CS) coated prussian blue nanoparticles (PBNPs) or cadmium hexacyanoferrate nanoparticles (CdNPs) and loaded with AuNPs were used as distinguishable signal tags. The resulting immunosensor exhibited high selectivity and sensitivity in simultaneous determination of CEA and AFP in a single run. The linear ranges were from 0.01 to 100 ng mL(-1) for both CEA and AFP. The detection limits reached 0.01 ng mL(-1) for CEA and 0.006 ng mL(-1) for APP, respectively. No obvious nonspecific adsorption and cross-talk was observed during a series of analyses to detect target analytes. In addition, for the detection of clinical serum samples, it is well consistent with the data determined by the ELISA, indicating that the immunosensor provides a possible application for the simultaneous multianalyte determination of CEA and AFP in clinical diagnostics. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:184 / 190
页数:7
相关论文