Antioxidative therapy has been considered an efficient strategy for the treatment of a series of excessive reactive oxygen species (ROS)-triggered diseases, including oxidative-stress-induced periodontal disease. However, current natural enzymes and nanozymes often show their high specificity toward given ROS and have insufficient antioxidative effects against multiple ROS generated in the diseases process. Meanwhile, multienzyme-based antioxidant defense systems are usually confined by the complicated synthesis as well as potential unwanted residue and toxicity. Various supports are highly needed to immobilize natural enzymes and antioxidants during the biorelated usages due to their low operational stability and difficulty of reuse. To overcome these limitations, we develop a high-performance platform by using biodegradable polydopamine nanoparticles (PDA NPs) as smart ROS scavengers in oxidative stress-induced periodontal disease. Although PDA-based materials are well-known to eliminate ROS both in vitro and in vivo, their antioxidative performance in periodontal disease and relative mechanisms have yet to be well-explored. In this study, PDA NPs can act as ROS scavengers in dental specialties with ideal outcomes. Spectroscopic and in vitro experiments provide strong evidence for the roles of PDA NPs in scavenging multiple ROS and suppressing ROS-induced inflammation reactions. In addition to the above investigations, the results from a murine periodontitis model clearly demonstrate the feasibility of PDA NPs as robust antioxidants with which to remove ROS and decrease periodontal inflammation without any side effects. Taken together, the results from our present study will provide valuable insight into the development of safe and efficient antioxidant defense platforms for further biomedical uses.

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Herein, ruthenium (Ru) and iridium (Ir) are introduced to tailor the atomic and electronic structure of self-supported nickel-vanadium (NiV) layered double hydroxide to accelerate water splitting kinetics, and the origin of high hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) activities are analyzed at atomic level. X-ray photoelectron spectroscopy and X-ray absorption near-edge structure spectroscopy studies reveal synergistic electronic interactions among Ni, V, and Ru (Ir) cations. Raman spectra and Fourier and wavelet transform analyses of the extended X-ray absorption fine structure indicate modulated local coordination environments around the Ni and V cations, and the existence of V vacancies. The Debye–Waller factor suggests a severely distorted octahedral V environment caused by the incorporation of Ru and Ir. Theoretical calculations further confirm that Ru or Ir doping could optimize the adsorption energy of intermediates in the Volmer and Heyrovsky steps for HER and accelerate the whole kinetic process for OER.