Natural down fiber-reinforced and polypyrrole-modified silk fibroin composite aerogel for efficient solar steam generation toward seawater desalination and wastewater treatment.

Poor mechanical properties and low photothermal efficiency of silk fibroin (SF)-based aerogels are current challenges that need to be addressed. Herein, SF composite aerogel was developed to enhance the mechanical properties through physical interpenetration of natural down fiber (Df) and hydrogen bonds formed among SF, Df, and polypyrrole (PPy) and to improve the evaporation performance via in-situ polymerization of PPy. The resultant Df/PPy@SF aerogel showed significant improvement of compressive stress (194.29 kPa), which was 6.96 times than that of SF aerogel (27.91 kPa), and also good compression resiliency. Furthermore, due to uniform distribution of PPy and high porosity of 95.27 %, Df/PPy@SF aerogel possessed high light absorbance of 99.87 % and low thermal conductivity (0.043 W·m-1·K-1). Thus, the Df/PPy@SF aerogel evaporator demonstrated high evaporation rates of 2.12 kg·m-2·h-1 for 3.5 wt% saline water, 2.04-2.15 kg·m-2·h-1 for various dye water, and 2.10 kg·m-2·h-1 for actual dye wastewater. Moreover, the developed aerogel exhibited evaporation stability and outstanding salt-resistance when treating seawater due to continuous water supply by superhydrophilic porous aerogel. Therefore, these findings demonstrate the excellent performance of Df/PPy@SF aerogel and will inspire further research on developing natural fiber-reinforced aerogels for use in the fields of solar water evaporation, energy, and other related applications.

Desktop-stereolithography 3D printing of a radially oriented extracellular matrix/mesenchymal stem cell exosome bioink for osteochondral defect regeneration.

Mitochondrial dysfunction and oxidative stress damage are hallmarks of osteoarthritis (OA). Mesenchymal stem cell (MSC)-derived exosomes are important in intercellular mitochondria communication. However, the use of MSC exosomes for regulating mitochondrial function in OA has not been reported. This study aimed to explore the therapeutic effect of MSC exosomes in a three dimensional (3D) printed scaffold for early OA therapeutics. Methods: We first examined the mitochondria-related proteins in normal and OA human cartilage samples and investigated whether MSC exosomes could enhance mitochondrial biogenesis in vitro. We subsequently designed a bio-scaffold for MSC exosomes delivery and fabricated a 3D printed cartilage extracellular matrix (ECM)/gelatin methacrylate (GelMA)/exosome scaffold with radially oriented channels using desktop-stereolithography technology. Finally, the osteochondral defect repair capacity of the 3D printed scaffold was assessed using a rabbit model. Results: The ECM/GelMA/exosome scaffold effectively restored chondrocyte mitochondrial dysfunction, enhanced chondrocyte migration, and polarized the synovial macrophage response toward an M2 phenotype. The 3D printed scaffold significantly facilitated the cartilage regeneration in the animal model. Conclusion: This study demonstrated that the 3D printed, radially oriented ECM/GelMA/exosome scaffold could be a promising strategy for early OA treatment.