posted on 2018-10-18, 00:00authored byFei Wu, Hanjun Cheng, Huan Wei, Tianyi Xiong, Ping Yu, Lanqun Mao
Understanding
the real-time correlation between chemical patterns
and neural processes is critical for deciphering brain function. Voltammetry
has enabled this task but with a number of challenges for current-based
electrolysis in vivo. Herein, we report galvanic redox potentiometry
(GRP) potentially as a universal strategy for in vivo monitoring of
neurochemicals, with ascorbic acid (AA) as a typical example. The
GRP sensor is constructed on a self-driven galvanic cell configuration,
where AA is spontaneously oxidized at the indicating single-walled
carbon nanotube-modified carbon fiber electrode (SWNT-CFE), while
oxygen reduced at the laccase-modified reference CFE (Lac-CFE). At
thermodynamic equilibrium, open-circuit potential (OCP) can be a linear
indicator of the concentration of AA. The resulting sensor shows a
high selectivity to AA dynamics in the presence of coexisting electroactive
neurochemicals, which is mainly determined by the driving force for
the cell reaction, as suggested by principal investigation. Sensing
sensitivity of this OCP-based GRP method is not affected by nonspecific
protein adsorption and electrode fouling. Moreover, a micropipette
compartment of the reference electrode is designed to suppress mass
crossover and prevent disturbance to oxygen reduction through confinement
effect. The in vivo application of the GRP sensor is illustrated by
measuring the basal level of cortical AA in live rat brain (230 ±
40 μM) and its dynamics during ischemia/reperfusion. The GRP
concept is demonstrated as a prominent method for in vivo, real-time,
quantitative analysis of brain neurochemistry.