4.8 Article

An optical fiber-based LSPR aptasensor for simple and rapid in-situ detection of ochratoxin A

Journal

BIOSENSORS & BIOELECTRONICS
Volume 102, Issue -, Pages 504-509

Publisher

ELSEVIER ADVANCED TECHNOLOGY
DOI: 10.1016/j.bios.2017.11.062

Keywords

Localized surface plasmon resonance (LSPR); Sensing; Optical fiber; in situ; Aptamer; Ochratoxin A (OTA)

Funding

  1. Technology Innovation Program - Ministry of Trade, Industry & Energy (MI, Korea) [10060155]
  2. GRL Program - Ministry of Science, ICT and Future Planning of the Republic of Korea [NRF-2013K1A1A2A02050616]
  3. Research on Advanced Optical Science and Technology grant - GIST

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Label-free biosensing methods that rely on the use of localized surface plasmon resonance (LSPR) have attracted great attention as a result of their simplicity, high sensitivity, and relatively low cost. However, in-situ analysis of real samples using these techniques has remained challenging because colloidal nanoparticles (NPs) can be unstable at certain levels of pH and salt concentration. Even in the case of a chip-type LSPR sensor that can resolve the instability problem by employing NPs immobilized on the substrate, loading of a sample to sensor chip with exact volume control can be difficult for unskilled users. Herein, we report an optical-fiber-based LSPR aptasensor that can avoid these problems and serve as a portable and simple system for sensitive detection of a small mycotoxin,, ochratoxin A (OTA), in real samples. The optical fiber coated with aptamer-modified gold nanorods (GNRs) is simply dipped into a solution containing OTA and subjected to LSPR analysis. Quantitative analysis of OTA is performed by measuring the spectral red shift of the LSPR peak of GNRs. Under optimized conditions, the LSPR peak shift displays a linear response (R-2 = 0.9887) to OTA in the concentration range from 10 pM to 100 nM, with a limit of detection of 12.0 pM (3 S). The developed sensor shows a high selectivity for OTA over other mycotoxins such as zearalenone (ZEN) and ochratoxin B (OTB), and shows an accurate detection capability for OTA in real grape juice samples.

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