Biomolecule-functionalized magnetic nanoparticles for flow-through quartz crystal microbalance immunoassay of aflatoxin B sub(1)

A flow-through quartz crystal microbalance (QCM) immunoassay method has been developed based on aflatoxin B sub(1) antibody (anti-AFB sub(1))-functionalized magnetic core-shell Fe sub(3)O sub(4)/SiO sub(2 ) composite nanoparticles (bionanoparticles) in this study. To construct such an assay protocol...

Full description

Saved in:
Bibliographic Details
Published inBioprocess and biosystems engineering Vol. 32; no. 1; pp. 109 - 116
Main Authors Wang, Li, Gan, Xian-Xue
Format Journal Article
LanguageEnglish
Published 01.01.2009
Online AccessGet full text

Cover

Loading…
More Information
Summary:A flow-through quartz crystal microbalance (QCM) immunoassay method has been developed based on aflatoxin B sub(1) antibody (anti-AFB sub(1))-functionalized magnetic core-shell Fe sub(3)O sub(4)/SiO sub(2 ) composite nanoparticles (bionanoparticles) in this study. To construct such an assay protocol, anti-AFB sub(1), as a model protein, was initially covalently immobilized onto the Fe sub(3)O sub(4)/SiO sub(2 ) surface, and then the functionalized nanoparticles were attached to the surface of the QCM probe with an external magnet. The binding of target molecules onto the immobilized antibodies decreased the sensor's resonant frequency, and the frequency shift was proportional to the AFB sub(1) concentration in the range of 0.3-7.0ng/ml. The regeneration of the developed immunosensor was carried out via attaching or detaching the external magnet from the detection cell. In addition, the selectivity, reproducibility, and stability of the proposed immunoassay system were acceptable. Compared with the conventional ELISAs, the proposed immunoassay system was simple and rapid without multiple labeling and separation steps. Importantly, the proposed immunoassay method could be further developed for the immobilization of other antigens or biocompounds.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
content type line 23
ObjectType-Feature-2
ISSN:1615-7591
1615-7605
DOI:10.1007/s00449-008-0228-2