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Matrix deposition plays a critical role in image quality of matrix-assisted laser desorption/ionization mass spectrometry imaging (MALDI-MSI). To improve the ionization efficiency and overcome the limitation of traditional matrix deposition methods in the face of difficult-to-sublimate or difficult-to-dissolve matrix, covalent organic frameworks (COFs) named COF-DhaTab was successfully synthesized and firstly used as matrix film. It was fabricated by imprinting of sieved COF-DhaTab powder on the surface of a double-sided adhesive tape. Outstanding reproducibility and uniformity of COF-DhaTab film were demonstrated by relative standard deviation (RSD) within 8.37% and 7.71% from dot-to-dot and plate-to-plate, respectively. With the introduction of double-sided adhesive tape, water contact angle (WCA) of COF-DhaTab film increased from 55° to 141°, resulting in significant suppression of analyte diffusion. Moreover, the intensity of potassium perfluorooctanic sulfonate (PFOS, C 8 F 17 SO 3 −, m/z 498.93) was 9.3 × 105, more than six hundred times higher than that using DHB matrix. This enhancement was attributed to the rough surface and multiple branches of the synthesized COF-DhaTab. To verify the ability of COF-DhaTab film as substrate, the spatial distribution of PFOS in zebrafish, rat liver and kidney tissues was explored. Superior imaging capability was displayed with high-spatial resolution and reliable location distribution. These results not only demonstrate the outstanding ability of COF-DhaTab as matrix for MALDI-MS and MALDI-MSI, but also provide a facile approach for fabrication of novel matrix films for MALDI-MSI. [Display omitted] • A novel strategy was developed to fabricate matrix film for difficult-to-sublimate or difficult-to-dissolve matrix. • MALDI-MS signal of PFOS with COF-DhaTab matrix was increased by 600 times than DHB matrix. • Matrix film of sieved COF-DhaTab was used to study spatial distribution of PFOS by MALDI-MSI. • Excellent MALDI image quality was demonstrated by COF-DhaTab matrix film. [ABSTRACT FROM AUTHOR]

[Display omitted] • Industrialization of ultra-robust hybrid aerogels with micro-nano structure. • Recycling waste resources was a green and sustainable development strategy. • The multiscale interpenetrating networks acted as effective thermal isolation barriers. • Decoration of ZIF-8 crystals on the cross-linking points of nanofibers induced constructing rigid-flexible frameworks. • The hybrid aerogel exhibited remarkable mechanical, thermal isolation, gas and dye adsorption capacities. Ultra-low density nanoaerogels as the lightest solid material have aroused extensive attention. However, lacking crack extension resistance limited their further development and application. Here, aramid and cellulose wastes were recycled to prepare high value-added nanofibers, which were further self-assembled to construct multilfunctional hybrid aerogels. In-situ growth of zeolitic imidazolate frameworks-8 (ZIF-8) on the cellulose nanofiber (CNF) created a robust skeleton. Flexible aramid nanofibers (ANF), as burgeoning building blocks were employed to inlay into the microscopic skeleton structure for establishing micro-nano double networks. Benefiting from the existence of multiscale networks, the maximum value in the compressive stress of S 0 , S 1 , S 2 and S 3 increased from 2.74 to 4.63, 5.19 and 6.61 MPa, respectively. Meanwhile, ANF-ZIF-8-CNF hybrid aerogels exhibited low thermal conductivity of 3.58–3.97 × 10-2 W/(m⋅K). The significant increase in the specific surface area (481.46 m2/g) endowed hybrid aerogels with high adsorption abilities for nitrogen (280.83 cm3/g), prussian blue (34.12 mg⋅g−1), rhodamine B (37.30 mg⋅g−1), DMF (25.13 g⋅g−1) and DMSO (15.48 g⋅g−1), respectively. This multiscale structural engineering strategy opens an avenue toward to upcycle waste resources into the next-generation high-performance nanoaerogels, showing huge application potential in thermal management, air purification and sewage treatment. [ABSTRACT FROM AUTHOR]

[Display omitted] • Biomimetic fabrication bioprinting strategies based on decellularized extracellular matrix are reviewed. • Fabrication of decellularized extracellular matrix and common 3D Bioprinting Techniques are summarized. • Decellularized extracellular matrix-based bioprinting for musculoskeletal tissue regeneration is overviewed. • The challenge and future perspectives of bioprinting strategies based on decellularized extracellular matrix are prospected. Musculoskeletal disorders, as one of the prevalent categories of ailments, exert significant impacts on individuals' lives, occupations, and physical activities. Degenerative changes, injuries, infections, and tumor resections causing defects in musculoskeletal tissues such as cartilage, bones, skeletal muscles, menisci, ligaments, and rotator cuffs can detrimentally affect patients' quality of life and mental well-being. Traditional autologous and allogeneic transplantations have been clinically employed. However, autologous transplantation suffers from the limitation of a finite number of transplantable tissues, while allogeneic transplantation faces challenges such as immune rejection. The extracellular matrix (ECM) serves as a natural scaffold for cells to fulfill physiological functions such as adhesion, proliferation, and differentiation. Decellularized extracellular matrix (dECM) emerges as a promising biomaterial generated through specific tissue or organ decellularization. Leveraging 3D bioprinting technology, dECM-based biomaterials enable customized printing and construction. This study reviews various decellularization techniques, post-decellularization strategies, and commonly used 3D bioprinting technologies. It summarizes the integration of dECM-based biomaterials with 3D bioprinting technology applied in musculoskeletal system research. These investigations showcase the exciting potential of dECM-based biomaterials in the musculoskeletal system, offering prospects for clinical translation in orthopedics. [ABSTRACT FROM AUTHOR]

• The energy bands of Fe and Mn co-adsorbed monolayers of SnSe 2 exhibit semi-metallicity. • As tensile strain increases, the adsorption system transitions from semi-metallic to metallic, accompanied. • The co-adsorption system's curie temperature is calculated to be 205.2 K. • The application of Fe and Mn double transition metal atoms to monolayer SnSe 2 may have potential. Pure 2D SnSe 2 is not magnetic, which limits its application in spintronics. However, magnetic properties can be induced in pure 2D SnSe 2 by introducing transition metal elements. In this study, we used first-principles calculations based on density-functional theory to predict the electronic structure and magnetic properties of monolayer SnSe 2 under adsorption of Fe and Mn double transition metal atoms. Our findings show that the energy bands of Fe and Mn co-adsorbed monolayers of SnSe 2 exhibit semi-metallicity. As tensile strain increases, the adsorption system transitions from semi-metallic to metallic, accompanied by an increase in total magnetic moment. Based on the Heisenberg model, the co-adsorption system's Curie temperature is calculated to be 205.2 K. Our studies suggest that the application of Fe and Mn double transition metal atoms to monolayer SnSe 2 may have potential in spintronics. [ABSTRACT FROM AUTHOR]

Accurate determination of the electrostatic force exerted on multipole moments is essential in comprehending the interaction between charged bodies and dielectric layers. A comprehensive solution is presented in this study for the calculation of the electric potential, field, and force generated by n th-order electric multipole above a semi-infinite dielectric body covered by a dielectric layer using the image multipole method. The present study investigates the impact of dielectric thickness, permittivity, and separation distance on the electrostatic interaction between an electric multipole moment and a semi-infinite dielectric body. The calculation results indicate that as the thickness of the dielectric layer increases and the dielectric constant of the surrounding medium surpasses that of the dielectric layer, the electrostatic attractive force undergoes a transition to a repulsive force. The magnitude of the electrostatic force acting on a n th-order electric multipole moment is directly proportional to the square of the value of the electric multipole moment and inversely proportional to the 2 (n +1) power of the distance. [ABSTRACT FROM AUTHOR]

Nowadays, two-dimensional materials are ideal for fabricating optoelectronic and spintronic devices. We have investigated the optical and magnetic properties of −6 % to 6 % strain on Mn-adsorbed monolayer SnSe 2 films using a first-principles approach. The Mn-adsorbed monolayer SnSe 2 is a magnetic semiconductor in the absence of strain effects. As the tensile strain increases, the band gap of the Mn-adsorbed monolayer SnSe 2 decreases and the structure becomes unstable, and Mn adsorption changes to exothermic adsorption at −6 % strain. The magnetic moment of the system increases slightly with increasing tensile strain and decreases rapidly when the strain reaches 4%. As the compressive strain increases, the magnetic moment first decreases slightly and then decreases rapidly when the strain reaches −4 %. Calculations of the optical properties show that the static dielectric constants at −6 %, −4 %, −2 %, 0 %, 2 %, 4 % and 6 % strains are 15.23, 10.19, 8.67, 7.78, 6.38, 5.99 and 5.92, respectively, which increase with increasing compressive strain. It decreases with increase in tensile strain. The static dielectric function increases as the compressive strain increases and decreases as the tensile strain increases. In the visible light region, the reflectivity, refractive index, extinction coefficient and photoconductivity in the XX and ZZ directions increase with increasing tensile strain. Our study shows that the optoelectronic and magnetic properties of the SnSe 2 adsorbed Mn system can be improved to some extent by applying strain, and this study is expected to provide theoretical guidance for the fabrication of SnSe 2 -based magnetic optoelectronic devices. [ABSTRACT FROM AUTHOR]

Alzheimer's disease (AD) is a chronic neurodegenerative disease with high prevalence, long duration and poor prognosis. The blood-brain barrier (BBB) is a physiologic barrier in the central nervous system, which hinders the entry of most drugs into the brain from the blood, thus affecting the efficacy of drugs for AD. Natural products are recognized as one of the promising and unique therapeutic approaches to treat AD. To improve the efficiency and therapeutic effect of the drug across the BBB, a natural polyphenolic compound, procyanidin C-1 (C1) was encapsulated in glucose-functionalized bovine serum albumin (BSA) nanoparticles to construct Glu-BSA/C1 NPs in our study. Glu-BSA/C1 NPs exhibited good stability, slow release, biocompatibility and antioxidant properties. In addition, Glu-BSA/C1 NPs penetrated the BBB, accumulated in the brain by targeting Glut1, and maintained the BBB integrity both in vitro and in vivo. Moreover, Glu-BSA/C1 NPs alleviated memory impairment of 5 × FAD mice by reducing Aβ deposition and Tau phosphorylation and promoting neurogenesis. Mechanistically, Glu-BSA/C1 NPs significantly activated the PI3K/AKT pathway and inhibited the NLRP3/Caspase-1/IL-1β pathway thereby suppressing neuroinflammation. Taken together, Glu-BSA/C1 NPs could penetrate the BBB and mitigate neuroinflammation in AD, which provides a new therapeutic approach targeting AD. Schematic illustration of the synthesis and application of Glu-BSA/C1 NPs in a mouse model of Alzheimer's disease. [Display omitted] [ABSTRACT FROM AUTHOR]

The adverse microenvironment, including neuroinflammation, hinders the recovery of spinal cord injury (SCI). Regulating microglial polarization to alleviate neuroinflammation at the injury site is an effective strategy for SCI recovery. MG53 protein exerts obvious repair ability on multiple tissues damage, but with short half-life. In this study, we composited an innovative MG53/GMs/HA-Dex neural scaffold using gelatin microspheres (GMs), hyaluronic acid (HA), and dextran (Dex) loaded with MG53 protein. This novel neural scaffold could respond to MMP-2/9 protein and stably release MG53 protein with good physicochemical properties and biocompatibility. In addition, it significantly improved the motor function of SCI mice, suppressed M1 polarization of microglia and neuroinflammation, and promoted neurogenesis and axon regeneration. Further mechanistic experiments demonstrated that MG53/GMs/HA-Dex hydrogel inhibited the JAK2/STAT3 signaling pathway. Thus, this MG53/GMs/HA-Dex neural scaffold promotes the functional recovery of SCI mice by alleviating neuroinflammation, which provides a new intervention strategy for the neural regeneration and functional repair of SCI. Schematic illustration of the preparation and application of MG53/GMs/HA-Dex neural scaffolds in a mouse model of spinal cord injury. [Display omitted] • MGHD responded to MMP-2/9 and stably released MG53 protein with good physicochemical properties and biocompatibility. • MGHD improved the motor function of SCI mice, suppressed neuroinflammation, and promoted neurogenesis and axon regeneration. • MGHD inhibited the JAK2/STAT3 signaling pathway. [ABSTRACT FROM AUTHOR]

[Display omitted] • Bomidin is a new recombinant antimicrobial peptide AMP derived from BMAP-27. • Bomidin mediates Keap1 protein degradation, enhancing Nrf2 nuclear translocation. • Bomidin can suppress ferroptosis, further relieving periodontitis. • Bomidin is a promising medicine for periodontitis. Periodontitis is a prevalent oral immunoinflammatory condition that is distinguished by the compromised functionality of periodontal ligament stem cells (PDLSCs). Bomidin, a new recombinant antimicrobial peptide (AMP), exhibits antibacterial properties and modulates immune responses. Nevertheless, the precise anti-inflammatory impact of bomidin in periodontitis has yet to be fully elucidated. Thus, the study aimed to clarified the role of bomidin in modulating inflammation and its underlying mechanisms. TNF-α was applied to treating PDLSCs for establishing a cell model of periodontitis. Bomidin, RSL3, ML385 and cycloheximide were also used to treat PDLSCs. Transcriptome sequencing, RT-qPCR, western blot, immunofluorescence, immunohistochemistry, Fe2+ detection probe, molecular docking, Co-IP assay, ubiquitination assay and murine models of periodontitis were used. Our study demonstrated that bomidin effectively suppressed inflammation in PDLSCs stimulated by TNF-α, through down-regulating the MAPK and NF-κB signaling pathways. Furthermore, bomidin exerted inhibitory effects on ferroptosis and activated the Keap1/Nrf2 pathway in the TNF-α group. There is a strong likelihood of bonding bomidin with Keap1 protein, which facilitated the degradation of Keap1 protein via the ubiquitin–proteasome pathway, leading to an enhanced translocation of Nrf2 protein to the nucleus. Bomidin can directly bond to Keap1 protein, resulting in the degradation of Keap1 through the ubiquitin–proteasome pathway, thereby further activating the Keap1/Nrf2 pathway. The upregulation of the Keap1/Nrf2 signaling pathway was found to contribute to the suppression of ferroptosis, ultimately alleviating inflammation in treatment of periodontitis. [ABSTRACT FROM AUTHOR]