Electromyography (EMG) is a widely used diagnostic technique for evaluating the electrical activity of muscles and their controlling nerves. However, conventional surface electrodes with planar structures often suffer from low spatial resolution and suboptimal signal quality. Here, 3D-shaped, substrate-free, soft, and biocompatible liquid metal electrodes (LMe) are presented as a wearable interface for neuromuscular signal recording. These electrodes enable the acquisition of high-quality EMG signals while their intrinsic mechanical softness supports long-term use in clinical settings. In a human pilot study, continuous, high-spatial-resolution EMG monitoring of musculoskeletal activity over 25 days is achieved. Furthermore, in vivo EMG monitoring in mouse models of ischemia and volumetric muscle loss demonstrated the therapeutic effects of extracellular muscle-rehabilitative drugs. This work highlights the potential of LMe for advanced drug screening and long-term clinical diagnostics.

Electronic retinal prostheses for stimulating retinal neurons are promising for vision restoration. However, the rigid electrodes of conventional retinal implants can inflict damage on the soft retina tissue. They also have limited selectivity due to their poor proximity to target cells in the degenerative retina. Here we present a soft artificial retina (thickness, 10 μm) where flexible ultrathin photosensitive transistors are integrated with three-dimensional stimulation electrodes of eutectic gallium-indium alloy. Platinum nanoclusters locally coated only on the tip of these three-dimensional liquid-metal electrodes show advantages in reducing the impedance of the stimulation electrodes. These microelectrodes can enhance the proximity to the target retinal ganglion cells and provide effective charge injections (72.84 mC cm^-2) to elicit neural responses in the retina. Their low Young's modulus (234 kPa), owing to their liquid form, can minimize damage to the retina. Furthermore, we used an unsupervised machine learning approach to effectively identify the evoked spikes to grade neural activities within the retinal ganglion cells. Results from in vivo experiments on a retinal degeneration mouse model reveal that the spatiotemporal distribution of neural responses on their retina can be mapped under selective localized illumination areas of light, suggesting the restoration of their vision.