A hydrogel for potential applications in wound dressing should possess several peculiar properties, such as efficient self-healing ability and mechanical toughness, so as to repair muscle and skin damage. Additionally, excellent cell affinity and tissue adhesiveness are also necessary for the hydrogel to integrate with the wound tissue in practical applications. Herein, an ultratough and self-healing hydrogel with superior cell affinity and tissue adhesiveness is prepared. The self-healing ability of the hydrogel is obtained through hydrogen bonds and dynamic Schiff cross-linking between dopamine-grafted oxidized sodium alginate (OSA-DA) and polyacrylamide (PAM) chains. The covalent cross-linking is responsible for its stable mechanical structure. The combination of physical and chemical cross-linking contributes to a novel hydrogel with efficient self-healing ability (80% mechanical recovery in 6 h), high tensile strength (0.109 MPa), and ultrastretchability (2550%), which are highly desirable properties and are superior to previously reported tough and self-healing hydrogels for wound dressing applications. More remarkably, due to plenty of catechol groups on the OSA-DA chains, the hydrogel has unique cell affinity and tissue adhesiveness. Moreover, we demonstrate the practical utility of our fabricated hydrogel via both in vivo and in vitro experiments.

Information recording and encryption/decryption functions are essential due to the prevalence of counterfeiting activities and information leakage in the current age. However, the development of high-resolution information recording and multistage information protection systems to achieve high data security levels, such as self-erasing encrypted data and time-controlled data handling, remains limited. Herein, inspired by the information-recording structure of paper, a multiresponsive nanofiber-reinforced poly(N-isopropylacrylamide) (PNIPAM) hydrogel (NCPN hydrogel) with improved mechanical properties, solvent-induced high-resolution reversible information recording, self-encryption, and multi-decryption capabilities, is proposed. Due to the unique hydrophilic and hydrophobic structures of the hydrogel matrix, ethanol and other polar analogs can be applied as special inks to record information by changing the lower critical solution temperature to achieve the repeatable transmittance variation. The recorded information can be erased via water wiping or ethanol volatilization. Additionally, self-encryption can be achieved and adjusted based on the ethanol volatilization time and concentration difference, and confidential information can be further decrypted in a water environment or under a thermal stimulus. Furthermore, several stable, repeatable, and fast-response hydrogel-based information-recognition systems are designed and investigated. Therefore, the designed hydrogel-based informational platform provides a universal information-handling system allowing for the reversible recording of information, with self-encryption and multidecryption capabilities.

The infection of orthopedic implantation devices with Staphylococcus is a serious concern within the biomaterial community. Treatments are not always successful because of antibiotic-resistant bacteria and serious biofilm infections. Human β-defensin 3 (hBD-3) is considered to be the most promising class of defensin antimicrobial peptides and its effect on antibiotic-resistant Staphylococcus biofilms, combined with ultrasound (US)-targeted microbubble (MB) destruction (UTMD), has not been reported. In the study, we found that biofilm densities, the percentage of live cells and the viable counts of two tested Staphylococcus recovered from the biofilm were significantly decreased in the maximum concentration hBD-3 combined with UTMD compared with those of any other groups. Furthermore, results suggested that UTMD could also enhance 1MIC hBD-3 activity inhibiting the biofilm-associated genes expression of icaAD and the methicillin-resistance genes expression of MecA by simultaneously promoting the icaR expression. UTMD may have great potential for improving antibiotic activity against biofilm infections.