4.8 Article

A label-free nanostructured plasmonic biosensor based on Blu-ray discs with integrated microfluidics for sensitive biodetection

Journal

BIOSENSORS & BIOELECTRONICS
Volume 96, Issue -, Pages 260-267

Publisher

ELSEVIER ADVANCED TECHNOLOGY
DOI: 10.1016/j.bios.2017.05.020

Keywords

Blu-ray disc; Plasmonic nanostructure; Integration; Microfluidics; Biosensing; Antibody

Funding

  1. CONACYT [225362]
  2. COLONTEST project (RETOS-COLABORACION Subprogram) [RTC-2014-1518-1]
  3. PreDICT project (Programa estatal de investigacion, desarrollo e innovacion orientada a los Retos de la Sociedad) [TEC2016-78515-R]
  4. Departament d'Universitats, Recerca i Societat de la Informacio de la Generalitat de Catalunya [2014 SGR 624]
  5. Severo Ochoa Centers of Excellence Program of Spanish MINECO [SEV-2013-0295]

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Nanostructure-based plasmonic biosensors have quickly positioned themselves as interesting candidates for the design of portable optical biosensor platforms considering the potential benefits they can offer in integration, miniaturization, multiplexing, and real-time label-free detection. We have developed a simple integrated nanoplasmonic sensor taking advantage of the periodic nanostructured array of commercial Blu-ray discs. Sensors with two gold film thicknesses (50 and 100 nm) were fabricated and optically characterized by varying the oblique-angle of the incident light in optical reflectance measurements. Contrary to the use normal light incidence previously reported with other optical discs, we observed an enhancement in sensitivity and a narrowing of the resonant linewidths as the light incidence angle was increased, which could be related to the generation of Fano resonant modes. The new sensors achieve a figure of merit (FOM) up to 35 RIU-1 and a competitive bulk limit of detection (LOD) of 6.3x10(-6) RIU. These values significantly improve previously reported results obtained with normal light incidence reflectance measurements using similar structures. The sensor has been combined with versatile, simple, ease to-fabricate microfluidics. The integrated chip is only 1 cm(2) (including a PDMS flow cell with a 50 mu m height microfluidic channel fabricated with double-sided adhesive tape) and all the optical components are mounted on a 10 cmx10 cm portable prototype, illustrating its facile miniaturization, integration and potential portability. Finally, to assess the label-free biosensing capability of the new sensor, we have evaluated the presence of specific antibodies against the GTF2b protein, a tumor-associate antigen (TAA) related to colorectal cancer. We have achieved a LOD in the pM order and have assessed the feasibility of directly measuring biological samples such as human serum.

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