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Fabrication and in vitro performance of a dual responsive lactate and glucose biosensor

Implantable multi-analyte biosensors are particularly challenging because the specificity of bioreceptors must be conferred to limited real estate. Additive biofabrication techniques based on electropolymerization for a dual responsive (glucose and lactate) biotransducer have been developed and char...

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Bibliographic Details
Published in:Electrochimica acta 2018-03, Vol.267, p.71-79
Main Authors: Kotanen, Christian N., Karunwi, Olukayode, Alam, Fouzan, Uyehara, Catherine F.T., Guiseppi-Elie, Anthony
Format: Article
Language:English
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Summary:Implantable multi-analyte biosensors are particularly challenging because the specificity of bioreceptors must be conferred to limited real estate. Additive biofabrication techniques based on electropolymerization for a dual responsive (glucose and lactate) biotransducer have been developed and characterized in vitro. Mediator modification of working microdisc electrode arrays with nickel hexacyanoferrate (NiHCF) followed by alternating layer-by-layer electropolymerization of polypyrrole-poly(styrene-sulfonic acid) (PPy-PSSA) and PPy-Enzyme (glucose oxidase or lactate oxidase) to a total applied charge density (QT = 50 or 100 mC/cm2 applied in Q = 5, 10 or 100 mC/cm2 increments) were evaluated for their contributions to a biosensor's bioanalytical performance. Single layered PPy-Enzyme (100 mC/cm2) biotransducers showed a higher sensitivity compared to all multi-layered biotransducers. An interceding layer of NiHCF at the Pt|PPy-GOx interface improved consistency in PPy-GOx electrodeposition compared to unmodified devices but, measured under self-consistent anodic conditions (0.65 V vs. Ag/AgCl), did not improve sensitivity. Electrochemical Impedance Spectroscopy (EIS) showed that the mediator layer did not change the overall impedance spectra of the Pt microelectrode array when compared to unmodified Pt electrodes. Under anodic test conditions, non-mediator modified devices had a higher sensitivity (0.94 nA/mM) to glucose than the mediator modified devices (0.32 nA/mM).
ISSN:0013-4686
1873-3859
DOI:10.1016/j.electacta.2018.02.042