Stimuli-responsive nanoparticles (NPs), so-called "smart" NPs, possess great potentials in drug delivery. Presently, the intelligence of smart NPs is mainly based on their chemical or physical changes to stimuli, which are usually "mechanical" and fundamentally different from biological intelligence. Inspired by mitochondria (MT), a biosmart nanoparticle with microenvironment targeting and self-adaptive capacity (MTSNP) was fabricated for ischemic tissue repair. The nanoparticles were designed as shell@circular DNA@ shell@core. The double shells were like the two-layered membranes of MT, the melatonin-loaded cores corresponded to the MT matrix, and the circular DNA corresponded to MTDNA. In function, melatonin-loaded cores simulated the cell-protective mechanism of MT, which naturally synthesized melatonin to resist ischemia, while circular DNA was constructed to mimic the biological oxygen-sensing mechanism, synthesizing VEGF for vascularization according to oxygen level, like the ATP supply by MT according to microenvironment demand. At the acute stage of ischemia, melatonin was rapidly released from MTSNP to scavenge reactive oxygen species and activated melatonin receptor I on MT to prevent cytochrome c release, which would activate apoptosis. During the chronic stage, circular DNA could sense hypoxia and actively secrete VEGF for revascularization as a response. Importantly, circular DNA could also receive feedback of revascularization and shut down VEGF secretion as an adverse response. Then, the therapeutic potentials of the MTSNP were verified in myocardial ischemia by the multimodality of the methods. Such nanoparticles may represent a promising intelligent nanodrug system.

Background The niche of tissue development in vivo involves the growth matrix, biophysical cues and cell-cell interactions. Although natural extracellular matrixes may provide good supporting for seeding cells in vitro, it is evitable to destroy biophysical cues during decellularization. Reconstructing the bioactivities of extracellular matrix-based scaffolds is essential for their usage in tissue repair. Results In the study, a hybrid hydrogel was developed by incorporating single-wall carbon nanotubes (SWCNTs) into heart-derived extracellular matrixes. Interestingly, insoluble SWCNTs were well dispersed in hybrid hydrogel solution via the interaction with extracellular matrix proteins. Importantly, an augmented integrin-dependent niche was reconstructed in the hybrid hydrogel, which could work like biophysical cues to activate integrin-related pathway of seeding cells. As supporting scaffolds in vitro, the hybrid hydrogels were observed to significantly promote seeding cell adhesion, differentiation, as well as structural and functional development towards mature cardiac tissues. As injectable carrier scaffolds in vivo, the hybrid hydrogels were then used to delivery stem cells for myocardial repair in rats. Similarly, significantly enhanced cardiac differentiation and maturation(12.5 ± 2.3% VS 32.8 ± 5%) of stem cells were detected in vivo, resulting in improved myocardial regeneration and repair. Conclusions The study represented a simple and powerful approach for exploring bioactive scaffold to promote stem cell-based tissue repair. Graphic abstract

There is a high demand for hydrogels with multifunctional performance (a combination of adhesive, mechanical, and electrical properties) in biological, tissue engineering, robotics, and smart device applications. However, a majority of existing hydrogels are relatively rigid and brittle, with limited stretchability; this hinders their application in the emerging field of flexible devices. In this study, cheap and abundant potato residues were used with polyacrylamide (PAM) to fabricate a multifunctional hydrogel, and chitosan was used for the design of a three-dimentional (3D) network-structured hydrogel. The as-prepared hydrogels exhibited excellent stretchability, with an extension exceeding 900% and a recovery degree of over 99%. Due to the combination of physical and chemical cross-linking properties and the introduction of dopamine, the designed hydrogel exhibits a remarkable self-healing ability (80% mechanical recovery in 2 h), high tensile strength (0.75 MPa), and ultra-stretchability (900%). The resultant products offer superior properties compared to those of previously reported tough and self-healing hydrogels for wound adhesion. Chitosan and potato residues were used as scaffold materials for the hydrogels with excellent mechanical properties. In addition, in vitro experiments show that these hydrogels feature excellent antibacterial properties, effectively hindering the reproduction of bacteria. Moreover, the ternary hydrogel can act as a strain sensor with high sensitivity and a gauge factor of 1.6. The proposed strategy is expected to serve as a reference for the development of green and recyclable conductive polymers to fabricate hydrogels. The proposed hydrogel can also act as a suitable strain sensor for bio-friendly devices such as smart wearable electronic devices and/or for health monitoring.

Mining activities has generated large amounts of mine tailings each year, and these tailings usually contain high concentrations of heavy metal pollutants, which not only cause serious damage to the local and surrounding soil ecosystems, but also harm human health via the transmission of food chain. Phytoremediation is treated as environmentally friendly, long-term effective and low-cost restoration method. However, tailing soil acidification, low organic matter content, poor water holding capacity and compaction make plant struggle to survive. Biochar, a soil conditioner can promote plant growth by improving the physical, chemical and biological properties of soil, thus strengthening the ability of phytoremediation in the contaminated tailings. This review elaborates how the physicochemical properties of biochar affect phytoremediation; and summarized how the raw materials of biochar affect the physicochemical characteristics. Finally, the future research directions are prospected.

A quantum dot bead based immunochromatographic assay was established for T-2 toxin with a limit of detection of 0.08 ng mL−1.