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An optical fiber-based LSPR aptasensor for simple and rapid in-situ detection of ochratoxin A.
Lee, Bobin; Park, Jin-Ho; Byun, Ju-Young; Kim, Joon Heon; Kim, Min-Gon.
Affiliation
  • Lee B; Department of Chemistry, School of Physics and Chemistry, Gwangju Institute of Science and Technology (GIST), Gwangju 61005, Republic of Korea.
  • Park JH; Advanced Photonics Research Institute, Gwangju Institute of Science and Technology (GIST), Gwangju 61005, Republic of Korea.
  • Byun JY; Hazards Monitoring Bionano Research Center, Korea Research Institute of Bioscience and Biotechnology (KRIBB), 125 Gwahak-ro, Yuseong-gu, Daejeon 34141, Republic of Korea.
  • Kim JH; Advanced Photonics Research Institute, Gwangju Institute of Science and Technology (GIST), Gwangju 61005, Republic of Korea. Electronic address: joonhkim@gist.ac.kr.
  • Kim MG; Department of Chemistry, School of Physics and Chemistry, Gwangju Institute of Science and Technology (GIST), Gwangju 61005, Republic of Korea. Electronic address: mkim@gist.ac.kr.
Biosens Bioelectron ; 102: 504-509, 2018 Apr 15.
Article in En | MEDLINE | ID: mdl-29197812
ABSTRACT
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 (R2 = 0.9887) to OTA in the concentration range from 10pM to 100nM, with a limit of detection of 12.0pM (3S). 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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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Biosensing Techniques / Aptamers, Nucleotide / Optical Fibers / Mycotoxins Type of study: Diagnostic_studies Language: En Journal: Biosens Bioelectron Journal subject: BIOTECNOLOGIA Year: 2018 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Biosensing Techniques / Aptamers, Nucleotide / Optical Fibers / Mycotoxins Type of study: Diagnostic_studies Language: En Journal: Biosens Bioelectron Journal subject: BIOTECNOLOGIA Year: 2018 Document type: Article