Journal
BIOSENSORS & BIOELECTRONICS
Volume 60, Issue -, Pages 52-56Publisher
ELSEVIER ADVANCED TECHNOLOGY
DOI: 10.1016/j.bios.2014.03.056
Keywords
Immunoassay; Octachlorostyrene; CdTe QDs; FRET
Categories
Funding
- National Basic Research Program of China [2009CB421601]
- National Science Foundation of China [21175038, 21235002]
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Octachlorostyrene (OCS), a persistent and bioaccumulative toxicant (PBT), was assayed by fluorescence immunoassay based on the Forster resonance energy transfer (FRET) between CdTe quantum dots (QDs) and rhodamine B-labeled OCS (RB-OCS). Anti-OCS antibody produced in this lab is adsorbed on a microtiter plate. The RB-OCS competes with OCS for the highly specific immunoreaction with the anti-OCS antibodies adsorbed on the microtiter plate. The solution is then isolated and mixed with CdTe QDs as fluorescent donor which excite the emission of RB-OCS through FRET. As a result, the emission of CdTe QDs at 530 nm decreases, whereas the emission of RB-OCS at 580 nm increases. The ratio of fluorescence intensity at 580 nm to that at 530 nm is proportional to the RB-OCS concentration at a fixed CdTe QDs concentration, and consequently proportional to the OCS concentration. Selective and sensitive responses to OCS are achieved with a linear range of 8-80 nM and a LOD of 3.8 nM. Because OCS is quantified based on the fluorescence ratio, the sensor-to-sensor difference is greatly eliminated, making the proposed method a useful approach for in site scanning of OCS. (C) 2014 Elsevier B.V. All rights reserved.
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