期刊
ANALYTICAL AND BIOANALYTICAL CHEMISTRY
卷 398, 期 6, 页码 2625-2634出版社
SPRINGER HEIDELBERG
DOI: 10.1007/s00216-010-3856-8
关键词
Microcystin-LR; Label-free biosensor; Self-assembled monolayer; Surface plasmon resonance
资金
- Madrid Regional Government [S-0505/AMB/0374]
- ESF
- ERDF
- Spanish MEC [CTQ2006-15610-C02]
- Complutense University [GR58-08]
- Academy of Sciences of the Czech Republic [KAN200670701]
- Ministry of Education, Youth and Sports [OC09058]
- MEC
A surface plasmon resonance (SPR) biosensor for the detection of microcystins (MCs) in drinking water has been developed. Several assay formats have been evaluated. The selected format is based on a competitive inhibition assay, in which microcystin-LR (MCLR) has been covalently immobilized onto the surface of an SPR chip functionalized with a self-assembled monolayer. The influence of several factors affecting sensor performance, such as the nature and concentration of the antibody, the composition of the carrier buffer, and the blocking and regeneration solutions, has been evaluated. The optimized SPR biosensor provides an IC(50) 0.67 +/- 0.09 A mu g L(-1), a detection limit of 73 A +/- 8 ng L(-1), and a dynamic range from 0.2 to 2.0 A mu g L(-1) for MCLR. Cross-reactivity to other related MCs, such as microcystin-RR (88%) and microcystin-YR (94%), has also been measured. The SPR biosensor can perform four simultaneous determinations in 60 min, and each SPR chip can be reused for at least 40 assay-regeneration cycles without significant binding capacity loss. The biosensor has been successfully applied to the direct analysis of MCLR in drinking water samples, below the provisional guideline value of 1 A mu g L(-1) established by the World Health Organization for drinking water.
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