We report a strategy to construct a dopaminereleasing gold surface mimicking a presynaptic membrane on a microfluidic chip to simulate in vivo neural signaling. We constructed dopamine self-assembled monolayers (DA SAMs) by electrochemical deprotection of methyl group-protected DA SAMs on a gold surface. Electrochemically controllable release of DA SAMs can be realized by applying nonhydrolytic negative potential on the gold surface. Our method in constructing DA SAMs avoids the polymerization and protonation of DA molecules which may lead to the failure of the DA SAM formation. By combining microfluidics, we realized spatial and temporal controllable release of DA by electrochemistry from the gold surface. Furthermore, by culturing neurons on the patterned DA SAMs, the interface between the DA SAMs and the neurons could serve as a presynaptic membrane, and the spatiotemporal release of DA could modulate the neuron activity with high precision. Our study holds great promise in the fields of neurobiology research and drug screening.

A smart nanofluidic device attracts attention as it enables to control the physicochemical properties and transportation phenomena, by using stimuli-responsive materials. This work reports a bioinspired modification of a conical ion track-etched polyethylene terephthalate nanopore surface by coating a layer of poly-L-lysine (PLL), which is a commonly used coating in biotechnology to achieve a dualresponsive nanofluidic channel by pH or temperature. The rectification of ionic transportation can be reversed by assembling PLL because of the change of surface bonds from the carboxyl to amine group. The PLL-modified nanopore becomes nonconductive as an "OFF" state at pH 11.5 and at a temperature of 70 °C in solution. The ionic transport in nanopores can be switched to the "ON" (conductive) state, by either decreasing pH or temperature. The transitions between "ON" and "OFF" states present excellent reversibility, which make the PLL-modified nanopores a promising smart nanofluidic device that can be used for drug delivery or biomimic ion/mass transport in future, besides the good biocompatibility and ease of use of PLL modification.

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