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The infection-prone wound pathology microenvironment leads to ulceration and difficult healing of diabetic wounds, which seriously affects the quality of survival of patients. In this study, natural polymer materials gelatin and polylysine were used as substrates. By introducing iron/tannic acid (Fe

Endoscopic submucosal dissection (ESD) is one of the most effective approaches for the minimally invasive treatment of early gastrointestinal cancers. Submucosal injections help safely and successfully remove lesions during ESD by elevating the mucosa and separating the submucosal muscle layer. Herein, we report dynamic injectable sodium alginate hydrogels (ISAHs) with shear-thinning for ESD surgery, which were easily fabricated by the sulfhydryl group of GSH-modified sodium alginate (SA-GSH) reacting with the aldehyde group of oxidized sodium alginate (OSA) at room temperature. ISAHs have advantageous self-healing abilities and antioxidant activity. Additionally, according to an in vitro test on porcine colorectal submucosal lifting, the submucosal elevation heights created by ISAHs were 13 % -18 % greater than those created by commercial ESD solutions (0.4 w/v% sodium hyaluronate). These properties and biocompatibility were confirmed in vitro and in vivo experiments. ISAHs will hopefully become a novel submucosal injectable hydrogel to assist ESD surgery.

A bio-fabricated nanocomposite hydrogel can catalyze excessive ROS into needed O2 and neutralize hypernomic MMPs in the pathological environment to promote diabetic wound healing.

The clinical acceleration of skin autogenous healing remains a great challenge, especially in the early stage after injury. In this work, a novel directly injectable hydrogel with high self-adaptability is designed as a provisional matrix to close the apposition of wound edges, using carboxymethyl cellulose and poly (γ-glutamic acid) through Schiff-base reaction. Benefiting from the dynamic covalent cross-linking structure, the functional biodegradable hydrogels are easy to prepare (gel time 5-180 s), demonstrating adequate mechanical strength (40-120 kPa), anti-fatigue abilities, and rapid self-healing (5-10 min at skin defect). Furthermore, the hydrogels exhibit biocompatibility and proliferation-promoting activity with murine fibroblasts. In the full-thickness dermal animal models, it significantly promoted collagen deposition, skin-function restoration, and VEGF expression. This hydrogel shows potential as a dressing available for skin regeneration during the healing of dermal injuries.

In this work, we systematically study the spectroscopic properties of Tb3+/Dy3+ co-doped phosphate glasses in the visible spectral region and explore the sensitization role of Dy3+ in the enhancement of visible fluorescence of Tb3+ ions. Judd-Ofelt parameters Ω2 and Ω4/Ω6 of the phosphate glass as host for Tb3+ are calculated as 21.60 × 10-20 cm2 and 0.73, respectively, based on the measured spectral absorption. Multiple energy transfer (ET) routes from Dy3+ to Tb3+ and their efficiencies are characterized, and the enhanced fluorescence properties of Tb3+ are investigated, including the emission spectral strength and the spontaneous emission lifetime as functions of Dy3+ doping concentration. The efficient nonradiative ET processes between Dy3+ and Tb3+ allow a moderate concentration level of Tb3+ to achieve favorably stronger spectral absorption at blue and ultraviolet wavelengths. Tb3+/Dy3+ co-doped phosphate glass shows promising potential for phosphors and lasing operation at visible wavelengths.

Tb3+ ions doped optical materials have emerged as gain media for green fiber lasers. Dy3+ ions were proposed as a sensitizer of Tb3+ ions in glasses to increase the excitation efficiency, yet a systematic understanding of the impact of Dy3+ doping on spectroscopic and physiochemical properties of glasses remains lacking. Here, using Tb3+/Dy3+ doped fluoride glass as a model system, we reveal that Dy3+ doping not only enhances Tb3+ emission intensity, but also increases the thermal stability of fluoride glasses. Detailed spectroscopic characterizations indicate that co-doping Dy3+ ions boosts visible luminescence intensity of Tb3+ ions in fluoride glasses due to sensitization of Tb3+ by Dy3+ ions. Importantly, we deeply research the energy transfer process, ascertain several important factors affecting energy transfer efficiency and propose optimal doping concentrations of Tb3+ and Dy3+ ions for visible emission. We envisage that our finding provides a new perspective for the synthesis of Tb3+-doped fluoride glasses with enhanced thermal stability, and may be extended for the fabrication of Tb3+-activated optical fibers.