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Inkjet-printed gold nanoparticle electrochemical arrays on plastic. Application to immunodetection of a cancer biomarker protein
被引:116
|作者:
Jensen, Gary C.
[1
]
Krause, Colleen E.
[1
]
Sotzing, Gregory A.
[1
,2
]
Rusling, James F.
[1
,2
,3
]
机构:
[1] Univ Connecticut, Dept Chem, Storrs, CT 06269 USA
[2] Univ Connecticut, Inst Mat Sci, Polymer Program, Storrs, CT 06269 USA
[3] Univ Connecticut, Ctr Hlth, Dept Cell Biol, Farmington, CT 06032 USA
关键词:
CARBON NANOTUBE FOREST;
SERUM INTERLEUKIN-6;
PROSTATE-CANCER;
AMPLIFICATION;
CARCINOMA;
IMMUNOSENSORS;
ELECTRONICS;
STRATEGIES;
BIOSENSORS;
DIAGNOSIS;
D O I:
10.1039/c0cp01755h
中图分类号:
O64 [物理化学(理论化学)、化学物理学];
学科分类号:
070304 ;
081704 ;
摘要:
Electrochemical detection combined with nanostructured sensor surfaces offers potentially low-cost, high-throughput solutions for detection of clinically significant proteins. Inkjet printing offers an inexpensive non-contact fabrication method for microelectronics that is easily adapted for incorporating into protein immunosensor devices. Herein we report the first direct fabrication of inkjet-printed gold nanoparticle arrays, and apply them to electrochemical detection of the cancer biomarker interleukin-6 (IL-6) in serum. The gold nanoparticle ink was printed on a flexible, heat resistant polyimide Kapton substrate and subsequently sintered to create eight-electrode arrays costing < 0.2 euro per array. The inkjet-printed working electrodes had reproducible surface areas with RSD < 3%. Capture antibodies for IL-6 were linked onto the eight-electrode array, and used in sandwich immunoassays. A biotinylated secondary antibody with 16-18 horseradish peroxidase labels was used, and detection was achieved by hydroquinone-mediated amperometry. The arrays provided a clinically relevant detection limit of 20 pg mL(-1) in calf serum, sensitivity of 11.4 nA pg(-1) cm(-2), and a linear dynamic range of 20-400 pg mL(-1).
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页码:4888 / 4894
页数:7
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