Integration of Faradaic electrochemical impedance spectroscopy into a scalable surface plasmon biosensor for in tandem detection
Author(s) -
Brandon Hong,
Alexander Sun,
Xin Lin,
A. G. Venkatesh,
Drew A. Hall,
Yeshaiahu Fainman
Publication year - 2015
Publication title -
optics express
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.394
H-Index - 271
ISSN - 1094-4087
DOI - 10.1364/oe.23.030237
Subject(s) - surface plasmon resonance , materials science , dielectric spectroscopy , biosensor , plasmon , detection limit , surface plasmon , analyte , optoelectronics , spectroscopy , analytical chemistry (journal) , electrode , nanotechnology , chemistry , nanoparticle , electrochemistry , chromatography , physics , quantum mechanics
We present an integrated label-free biosensor based on surface plasmon resonance (SPR) and Faradaic electrochemical impedance spectroscopy (f-EIS) sensing modalities, for the simultaneous detection of biological analytes. Analyte detection is based on the angular spectroscopy of surface plasmon resonance and the extraction of charge transfer resistance values from reduction-oxidation reactions at the gold surface, as responses to functionalized surface binding events. To collocate the measurement areas and fully integrate the modalities, holographically exposed thin-film gold SPR-transducer gratings are patterned into coplanar electrodes for tandem impedance sensing. Mutual non-interference between plasmonic and electrochemical measurement processes is shown, and using our scalable and compact detection system, we experimentally demonstrate biotinylated surface capture of neutravidin concentrations as low as 10 nM detection, with a 5.5 nM limit of detection.
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