A SPR-based immunosensor for the detection of isoproturon
The proof of principle of a reusable surface plasmon resonance (SPR)-based immunosensor for the monitoring of isoproturon (IPU), a selective and systemic herbicide, is presented. The detecting rat monoclonal anti-isoproturon antibody (mAb IOC 7E1) was reversibly immobilized through the use of a capt...
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Published in | Biosensors & bioelectronics Vol. 24; no. 6; pp. 1563 - 1568 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
Kidlington
Elsevier B.V
15.02.2009
Elsevier |
Subjects | |
Online Access | Get full text |
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Summary: | The proof of principle of a reusable surface plasmon resonance (SPR)-based immunosensor for the monitoring of isoproturon (IPU), a selective and systemic herbicide, is presented. The detecting rat monoclonal anti-isoproturon antibody (mAb IOC 7E1) was reversibly immobilized through the use of a capture mouse anti-rat (κ-chain) monoclonal antibody (mAb TIB 172), which was covalently immobilized on the sensor chip surface. Such strategy features a controlled binding of the captured detecting antibody as well as facilitates the surface regeneration. The capture of the anti-IPU mAb by the antibody (TIB 172) coated sensor surface could be carried out up to 120 times (immobilization/regeneration cycles) without any evidence of activity loss. With a high test midpoint and a low associated SPR signal, the direct detection format was shown to be unsuitable for the routine analysis of isoproturon. However, the limit of detection (LOD) could be easily enhanced by using a strategy based on a surface competition assay, which improved all immunosensor parameters. Moreover, the sensitivity and working range of the indirect format were found to be dependent on the surface density of the anti-IPU mAb IOC 7E1. As expected for competitive formats, the lowest surface coverage (0.5
ng/mm
2) allowed a lower detection of the herbicide isoproturon with a calculated LOD of 0.1
μg/l, an IC
50 (50% inhibition) of 5.3
±
0.6
μg/l, and a working range (20–80% inhibition) of 1.3–16.3
μg/l. |
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ISSN: | 0956-5663 1873-4235 |
DOI: | 10.1016/j.bios.2008.08.005 |