One-step synthesis of potassium ferricyanide-doped polyaniline nanoparticles for label-free immunosensor

• Published in: Biosensors & bioelectronics Vol. 68; pp. 462 - 467
• Main Authors: He, Sijing, Wang, Qiyou, Yu, Yanyan, Shi, Qiujia, Zhang, Lin, Chen, Zuanguang
• Format: Journal Article
• Language: English
• Published: England 15.06.2015
• Subjects: adsorption; aniline; Aniline Compounds - chemical synthesis; Aniline Compounds - chemistry; Antibodies; Antibodies - chemistry; Antibodies - immunology; Antigens; Biosensing Techniques; Carcinoembryonic Antigen - chemistry; Carcinoembryonic Antigen - immunology; Carcinoembryonic Antigen - isolation & purification; Charging; Chitosan - chemistry; detection limit; electrodes; Ferricyanides - chemical synthesis; Ferricyanides - chemistry; Gold; Gold - chemistry; Humans; Immunoassay - methods; immunoassays; Immunosensors; Limit of Detection; Metal Nanoparticles - chemistry; nanogold; Nanoparticles; oxidants; Polyanilines; polymerization; Surface chemistry; Carcinoembryonic antigen; Label-free immunosensor; Potassium ferricyanide-doped polyaniline nanoparticles; Gold nanoparticles; One-step synthesis
• ISSN: 0956-5663; 1873-4235; 1873-4235
• DOI: 10.1016/j.bios.2015.01.018

A novel, label-free and inherent electroactive redox immunosensor for ultrasensitive detection of carcinoembryonic antigen (CEA) was proposed based on gold nanoparticles (AuNPs) and potassium ferricyanide-doped polyaniline (FC-PANI) nanoparticles. FC-PANI composite was synthesized via oxidative polymerization of aniline, using potassium ferricyanide (K3[Fe(CN)6]) as both oxidant and dopant. FC-PANI acting as the signal indicator was first fixed on a gold electrode (GE) to be the signal layer. Subsequently, the negatively charged AuNPs could be adsorbed on the positively charged FC-PANI modified GE surface by electrostatic adsorption, and then to immobilize CEA antibody (anti-CEA) for the assay of CEA. The CEA concentration was measured through the decrease of amperometric signals in the corresponding specific binding of antigen and antibody. The wide linear range of the immunosensor was from 1.0 pg mL(-1) to 500.0 ng mL(-1) with a low detection limit of 0.1 pg mL(-1) (S/N=3). The proposed method would have a potential application in clinical immunoassays with the properties of facile procedure, stability, high sensitivity and selectivity.