pharmaceutical drug delivery and healthcare systems. E-drugs are biocompatible electronic devices capable of identifying specific biological analytes (e.g., glucose, enzymes, and other biomolecules), [1,2] environmental stimuli (e.g., strain, pressure, and external temperature), and electrophysiological signals (e.g., electrocardiograms (ECG), electromyograms (EMG), and electroencephalography (EEG)) to monitor health status and deliver therapeutic treatments in a controlled manner via wireless prompts. [3][4][5] Owing to their innovative functions and technologies, e-drugs have been widely adopted in pharmaceutical and medical research to monitor and treat chronic diseases, which are still considered difficult to cure. Conventional pharmaceutical treatments or medical procedures for chronic diseases encounter a major obstacle in patient compliance, as they involve regular drug intake or treatments. [6] For example, patients with diabetes are recommended to collect blood samples to measure their glucose levels twice a day. However, the International Diabetes Management Practice Study reported that only 29.7-38.5% of patients with type-2 diabetes in Asia, Eastern Europe, and Latin America self-monitor their glucose levels, which hinders effective management of their condition. [7] As a strategy to improve patients' adherence to drug intake and treatments, electronic devices capable of continuously monitoring biological signal levels and therapeutic response via wireless applications have been demanded by the markets.The fundamental differences between electronics and biological tissues have emerged as a challenge in the development of an advanced generation of e-drugs. For instance, soft biological tissues have a low modulus of elasticity, which is typically less than 100 kPa, and high moisture content. By contrast, conventional electronics are generally made of electronic materials such as metals and silicone, which are stiff, with modulus greater than 80 GPa, dry, and static. [8] This mechanical and physical mismatch between human tissues and electronics causes adverse clinical outcomes. Major consequences include inflammatory responses induced by the micromotion of the implant, during and after implantation, as well as scar tissue and fibrotic encapsulation, which substantially compromises the performance and lifetime of e-drugs. [9,10] Recent advances in diagnostics and medicines emphasize the spatial and temporal aspects of monitoring and treating diseases. However, conventional therapeutics, including oral administration and injection, have difficulties meeting these aspects due to physiological and technological limitations, such as long-term implantation and a narrow therapeutic window. As an innovative approach to overcome these limitations, electronic devices known as electronic drugs (e-drugs) have been developed to monitor real-time body signals and deliver specific treatments to targeted tissues or organs. For example, ingestible and patch-type e-drugs could detect changes in biomarkers at the target s...