Poly(3,4-ethylenedioxythiophene) (PEDOT) has emerged as a promising neural interface material, but the weak adhesion of PEDOT to substrates adversely affects its reliability and practical application. Although adhesive interfacial layers have been explored to enhance the adhesion of PEDOT, their poor conductivity seriously compromises the performance of neural electrodes. It is a great challenge to develop an adhesive interfacial layer with excellent electrical properties. Herein, utilizing the advantages of polyindole derivatives, conductive polymers which have various functional groups for potential interface bonding, a conductive, adhesive, and biocompatible poly(5-nitroindole) (PIN-5NO 2 ) interfacial layer is developed to enhance the adhesion of PEDOT to metal electrodes. The conjugated PIN-5NO 2 with its superior electrical property can be prepared by electropolymerization of 5-nitroindole; however, the electrografting of amino groups, which is reduced from nitro groups in 5-nitroindole can provide strong adhesion with the gold (Au) substrate. With PIN-5NO 2 as an adhesive interfacial layer, the resultant Au/PIN-5NO 2 /PEDOT electrode exhibits excellent electrochemical property, superb stability, and biocompatibility for high-performance neural interface. The in vivo evaluation of Au/PIN-5NO 2 / PEDOT electrocorticographic microelectrodes demonstrates superior capacity to capture the neural dynamics of the brain. The novel strategy would offer a new insight for the construction of high-performance neural electrodes with high stability for neural interface application.

A robust neural interface with intimate electrical coupling between neural electrodes and neural tissues is critical for stable chronic neuromodulation. The development of bioadhesive hydrogel neural electrodes is a potential approach for tightly fixing the neural electrodes on the epineurium surface to construct a robust neural interface. Herein, we construct a photopatternable, antifouling, conductive (∼6 S cm–1), bioadhesive (interfacial toughness ∼100 J m–2), soft, and elastic (∼290% strain, Young’s modulus of 7.25 kPa) hydrogel to establish a robust neural interface for bioelectronics. The UV-sensitive zwitterionic monomer can facilitate the formation of an electrostatic-assembled conductive polymer PEDOT:PSS network, and it can be further photo-cross-linked into elastic polymer network. Such a semi-interpenetrating network endows the hydrogel electrodes with good conductivity. Especially, the photopatternable feature enables the facile microfabrication processes of multifunctional hydrogel (MH) interface with a characteristic size of 50 μm. The MH neural electrodes, which show improved performance of impedance, charge storage capacity, and charge injection capability, can produce effective electrical stimulation with high current density (1 mA cm–2) at ultralow voltages (±25 mV). The MH interface could realize high-efficient electrical communication at the chronic neural interface for stable recording and stimulation of a sciatic nerve in the rat model.

The poor contractility of the detrusor muscle in underactive bladders (UABs) fails to increase the pressure inside the UAB, leading to strenuous and incomplete urination. However, existing therapeutic strategies by modulating/repairing detrusor muscles, e.g., neurostimulation and regenerative medicine, still have low efficacy and/or adverse effects. Here, we present an implantable magnetic soft robotic bladder (MRB) that can directly apply mechanical compression to the UAB to assist urination. Composed of a biocompatible elastomer composite with optimized magnetic domains, the MRB enables on-demand contraction of the UAB when actuated by magnetic fields. A representative MRB for a UAB in a porcine model is demonstrated, and MRB-assisted urination is validated by in situ computed tomography imaging after 14-day implantation. The urodynamic tests show a series of successful urination with a high pressure increase and fast urine flow. Our work paves the way for developing MRB to assist urination for humans with UABs.