Abstract
The application of biosensors for near real-time monitoring of key energy and signaling molecules in the intact brain poses major challenges at a number of levels. In this context, amperometric biosensor functionality is impacted by a variety of physicochemical and biological phenomena, including enzyme substrate and co-substrate sensitivity, interference from endogenous electroactive species, fabrication and response consequences of miniaturization for tissue implantation, and biocompatibility issues. Polymer–enzyme composite (PEC) implantable microbiosensors, incorporating a poly-o-phenylenediamine (PoPD) ultrathin permselective barrier, possess a variety of characteristics which make them suitable for long-term in-vivo electrochemical (LIVE) monitoring. This chapter reviews the use of PoPD in this context, and describes a battery of PEC sensitivity and selectivity parameters which allow development of the basic design in a systematic way in order to understand and improve their performance, and to diversify the analyte range of these novel probes of brain function.
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Acknowledgements
This work was supported by funding from Science Foundation Ireland (SFI), the Irish Research Council for Science, Engineering and Technology (IRCSET), and by University College Dublin (UCD).
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O’Neill, R.D. (2013). Characterization of Polymer–Enzyme Composite Biosensors for Brain Monitoring In Vivo. In: Marinesco, S., Dale, N. (eds) Microelectrode Biosensors. Neuromethods, vol 80. Humana Press, Totowa, NJ. https://doi.org/10.1007/978-1-62703-370-1_6
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