Hearing loss, affecting individuals of all ages, can impair education, social function, and quality of life. Current treatments, such as hearing aids and implants, aim to mitigate these effects but often fall short in addressing the critical issue of accurately pinpointing sound sources. We report an intelligent hearing system inspired by the human auditory system: asymmetric well-aligned piezoelectric nanofibers combined with neural networks to mimic natural auditory processes. Piezoelectric nanofibers with spirally varying lengths and directions transmit and convert acoustic sound into mechanoelectrical signals, mimicking the complex cochlear dynamics. These signals are then encoded by digital neural networks, enabling accurate sound direction recognition. This intelligent hearing system surpasses human directional hearing, accurately recognizing sound directions horizontally and vertically. The advancement represents a substantial stride toward next-generation artificial hearing, harmonizing transduction and perception with a nature-inspired design. It promises for applications in hearing aids, wearable devices, and implants, offering enhanced auditory experiences for those with hearing impairments.

Light-driven soft actuators based on photoresponsive materials can be used to mimic biological motion, such as hand movements, without involving rigid or bulky electromechanical actuations. However, to our knowledge, no robust photoresponsive material with desireable mechanical and biological properties and relatively simple manufacture exists for robotics and biomedical applications. Herein, we report a new visible-light-responsive thermoplastic elastomer synthesized by introducing photoswitchable moieties (i.e., azobenzene derivatives) into the main chain of poly(ε-caprolactone) based polyurethane urea (PAzo). A PAzo elastomer exhibits controllable light-driven stiffness softening due to its unique nanophase structure in response to light, while possessing excellent hyperelasticity (stretchability of 575.2%, elastic modulus of 17.6 MPa, and strength of 44.0 MPa). A bilayer actuator consisting of PAzo and polyimide films is developed, demonstrating tunable bending modes by varying incident light intensities. Actuation mechanism via photothermal and photochemical coupling effects of a soft-hard nanophase is demonstrated through both experimental and theoretical analyses. We demonstrate an exemplar application of visible-light-controlled soft "fingers" playing a piano on a smartphone. The robustness of the PAzo elastomer and its scalability, in addition to its excellent biocompatibility, opens the door to the development of reproducible light-driven wearable/implantable actuators and lightweight soft robots for clinical applications.

Osteoarthritis leads to the progressive decay of articular cartilage. Due to its intrinsic avascular character, cartilage shows an inadequate capacity for regeneration. Cartilage loss may result in chronic pain, movement disorder and morbidity, which lack effective treatments except for joint replacement for late-stage osteoarthritis. To overcome this challenge, tissue engineering has emerged as a promising method. Scaffolds provide mechanical and biochemical support to stem cells that undergo differentiation and secrete a cartilage-specific matrix, and this strategy has been proven to have positive results. However, there is still a gap between the current strategy and perfection. Researchers are confronted with difficulties such as poor cell survival, insufficient differentiation, hypertrophy and endochondral calcification of neocartilage, and inadequate integration into the host tissue. The current research focuses on modifying scaffold parameters, including composition, stiffness, pore size, surface morphology, hydrophilicity and electric charge. On the other hand, cell regulation is another focus, including predifferentiation, gene editing, dynamic mechanical stimulus, and hypoxia. This review aims to provide a comprehensive discussion of existing challenges, scaffold types and properties, practical methods to improve chondrogenic potential and an outlook on future trends in cartilage bioengineering.

Skeletal muscle, which comprises a significant portion of the body, is responsible for vital functions such as movement, metabolism, and overall health. However, severe injuries often result in volumetric muscle loss (VML) and compromise the regenerative capacity of the muscle. Tissue-engineered muscles offer a potential solution to address lost or damaged muscle tissue, thereby restoring muscle function and improving patients’ quality of life. Induced pluripotent stem cells (iPSCs) have emerged as a valuable cell source for muscle tissue engineering due to their pluripotency and self-renewal capacity, enabling the construction of tissue-engineered artificial skeletal muscles with applications in transplantation, disease modelling, and bio-hybrid robots. Next-generation iPSC-based models have the potential to revolutionize drug discovery by offering personalized muscle cells for testing, reducing reliance on animal models. This review provides a comprehensive overview of iPSCs in tissue-engineered artificial skeletal muscles, highlighting the advancements, applications, advantages, and challenges for clinical translation. We also discussed overcoming limitations and considerations in differentiation protocols, characterization methods, large-scale production, and translational regulations. By tackling these challenges, iPSCs can unlock transformative advancements in muscle tissue engineering and therapeutic interventions for the future.

The fabrication of three-dimensional (3D) biostructures through additive manufacturing relies on the critical role of ink development. With the growing demand for high-resolution manufacturing, digital light processing (DLP) technology has emerged as a promising technique requiring specialised photosensitive inks. Although gelatine methacryloyl (GelMA) has been the primary option for DLP, its mechanical properties, biocompatibility, and low stability still present limitations. The development of collagen-based ink is thus in high demand for a wider stiffness adjustment range, native bioactivities, and versatility in biomedical engineering applications. In this paper, we report a rapid and low-cost protocol for collagen methacryloyl (ColMA)/poly(ethylene glycol) diacrylate (PEGDA) ink for DLP printing. The ink demonstrated the highest printing resolution of ∼50 μm by using 405 nm visible light. The printability, mechanical properties and cell viability of the DLP-printed ColMA/PEGDA structures were comprehensively evaluated. The printed ColMA/PEGDA structures reached a compressive modulus over 100 kPa with 0.6 wt% collagen. The printed ColMA/PEGDA scaffolds promoted the attachment and proliferation of 3 T3 fibroblasts, demonstrating their potential in future applications in biomedical engineering.