Individually addressable microelectrode arrays fabricated with gold-coated pencil graphite particles for multiplexed and high sensitive impedance immunoassays

• Published in: Biosensors & bioelectronics 2009-09, Vol.25 (1), p.34-40
• Main Authors: Zhang, Yun, Wang, Hua, Nie, Jinfang, Zhang, Yuwei, Shen, Guoli, Yu, Ruqin
• Format: Article
• Language: English
• Subjects: Antibodies, Immobilized - chemistry; Antibodies, Immobilized - immunology; Biological and medical sciences; Biotechnology; Electric Impedance; Fundamental and applied biological sciences. Psychology; General aspects; Gold - chemistry; Graphite - chemistry; Humans; Immobilization techniques; Immunoassay - methods; Immunoglobulin G - analysis; Immunoglobulin G - immunology; Methods. Procedures. Technologies; Microelectrode array; Microelectrodes; Multiplexed immunoassays; Nanoparticles - chemistry; Pencil graphite particles; Sensitivity and Specificity; Signal amplification; Site-selective immobilization
• ISSN: 0956-5663; 1873-4235
• DOI: 10.1016/j.bios.2009.06.011

A renewable, site-selective immobilization platform of microelectrode array (MEA) for multiplexed immunoassays has been initially developed using pencil graphite particles coated with gold layers as microelectrodes. The graphite particles available on the common pencil were utilized for directing the electro-deposition of gold layers with uniform microstructures which displayed a well-defined sigmoidal voltammetric response. In the concept-of-proof experiments, the resulting MEA platform was modified with functionalized monolayer, on which anti-human IgG antibodies could be stably immobilized in a site-selective way through binding chemistry to selectively capture human IgG antigens from the sample media. The subsequent introduction of anti-human IgG antibodies conjugated with 15 nm electro-active gold nanoparticles to recognize the captured IgG proteins resulted in a significant decrease in the interfacial electron-transfer resistance. High sensitive electrochemical quantification by gold nanoparticle-amplified impedance responses could thus be achieved. Experimental results show that the developed MEA sensor can allow for the detection of human IgG with wide linear range (0.05–100 ng ml −1) and sensitivity over 10 3 larger than that of the conventional, bulk gold electrode. The rapid regeneration of the used MEA platform can additionally be realized by a simple electrochemical treatment. The high selectivity of four individually addressable MEA platforms for multiple antigens in a single sample has been further demonstrated in the multiplexed immunoassay experiments. Such a site-selective immobilization strategy of MEA platform may open a new door towards the development of various simple, sensitive, cost-effective, and reusable biological sensors and biochips.