4.8 Article

Rapid fluorometric bacteria detection assay and photothermal effect by fluorescent polymer of coated surfaces and aqueous state

Journal

BIOSENSORS & BIOELECTRONICS
Volume 89, Issue -, Pages 1026-1033

Publisher

ELSEVIER ADVANCED TECHNOLOGY
DOI: 10.1016/j.bios.2016.10.027

Keywords

Fluorescent polymer; Quenching; Bacteria detection; Photothermal effect; Coated surface

Funding

  1. Ministry of Trade, Industry Energy (MOTIE) [10048377, 10062079, R0005237]
  2. Fusion Research R & D Program from the Korea Research Council for Industrial Science Technology [G02054]
  3. Basic Science Research Program through the National Research Foundation of Korea (NRF) - Ministry of Education [2014055946]
  4. Marine Biotechnology Program - Ministry of Oceans and Fisheries, South Korea [20150220]
  5. Korea Evaluation Institute of Industrial Technology (KEIT) [10062079, 10048377] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)
  6. Korea Institute of Marine Science & Technology Promotion (KIMST) [201502202] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)
  7. National Research Foundation of Korea [31Z20130012935] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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A fluorescent dye and a photothermal agent were grafted onto a cationic polymer for rapid and simple bacteria detection in liquid and solid phase based fluorescence on/off. The integrated poly(vinylpyrrolidone) (PVP) backbone with catechol and bromoethane moieties possesses unique optical properties due to the presence of boron dipyrromethane (BODIPY) and near infared NIR-responsive IR825 (F-PVP). The cationic segments showed distinct fluorescence quenching patterns after interaction with gram-positive and gram-negative bacteria via polyion complex interactions. Fluorescence quenching depended on direct interaction of the bacterial cell membrane, as confirmed using SEM and confocal imaging. The detection limit was 1 mg/mL for the liquid-phase assay and the minimal detectable concentration of bacteria using the solid-phase assay was 106 CFU/mL. After bacterial detection in contaminated area, our system can directly kill bacteria via the photothermal conversion ability of the IR825 substituent using NIR exposure by polymer solution and limited in coated PP. Finally, the proposed biosensor is capable as potential material for detection of bacteria in simple liquid and solid phase assay.

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