Fabrication Process Independent And Robust Aggregation Of Detonation Nanodiamonds In Aqueous Media

In the past detonation nanodiamonds (DNDs), sized 3–5 nm, have been praised for their colloidal stability in aqueous media, thereby attracting vast interest in a wide range of applications including nanomedicine. More recent studies have challenged the consensus that DNDs are monodispersed after their fabrication process, with their aggregate formation dynamics poorly understood. Here we reveal that DNDs in aqueous solution, regardless of their post-synthesis de-agglomeration and purification methods, exhibit hierarchical aggregation structures consisting of chain-like and cluster aggregate morphologies. With a novel characterization approach combining machine learning with direct cryo-transmission electron microscopy and with X-ray scattering and vibrational spectroscopy, we show that their aggregate morphologies of chain and cluster ratios and the corresponding size and fractal dimension distributions vary with the post-synthesis treatment methods. In particular DNDs with positive ζ-potential form to a hierarchical structure that assembles aggregates into large networks. DNDs purified with the gas phase annealing and oxidation tend to have more chain-like aggregates. Our findings provide important contribution in understanding the DND interparticle interactions to control the size, polydispersity and aggregation of DNDs for their desired applications

Fractal Structure of Hydrogels Modulates Stem Cell Behavior

Fractal dimension (<i>D</i>_f) is an index to describe the irregular continuous structure by quantifying the complexity. The concept of fractals has been employed to describe the complicated structure of polymer gel and human tissue. This study examined the effect of <i>D</i>_f on cell proliferation and stem cell differentiation in six polymer hydrogels with <i>D</i>_f ranging from 1.2 to 2.1. It was observed that fibroblasts and mesenchymal stem cells (MSCs) grew faster in hydrogels with higher <i>D</i>_f. Moreover, hydrogels with a fractal structure of <i>D</i>_f ≤ 1.4, ≥1.6, and ≥1.8 promoted the neural, osteogenic, and chondrogenic differentiation of MSCs, respectively. The fractal structure of gel can modulate cell proliferation and fate, which provides an insight into designing the appropriate fractal and molecular structure of polymer hydrogel for biomedical applications

Biodegradable Water-Based Polyurethane Shape Memory Elastomers for Bone Tissue Engineering

Shape memory polymers (SMPs) are polymers with the shape memory effect. The biodegradable SMPs are candidate materials for making biomedical devices and scaffolds for tissue engineering. Superparamagnetic iron oxide nanoparticles (SPIO NPs) have recently been reported to promote the osteogenic induction of human mesenchymal stem cells (hMSCs). In this study, we synthesized water-based biodegradable shape memory polyurethane (PU) as the main component of the 3D printing ink for fabricating bone scaffolds. The 3D printing ink contained 500 ppm of SPIO NPs to promote osteogenic induction and shape fixity, and it also contained polyethylene oxide (PEO) or gelatin for the improvement of printability. Scaffolds were printed by the microextrusion-based low-temperature fuse deposition manufacturing (LFDM) platform. Both PU–PEO and PU–gelatin ink showed excellent printability. Shape memory properties were evaluated in 50 °C air and 37 °C water. PU–PEO scaffolds showed better shape fixity and recovery than PU–gelatin scaffolds, while the shape memory properties in water were better than those in air. hMSCs were seeded for evaluation of bone regeneration. The proliferation of the hMSCs in PU/gelatin and PU/gelatin/SPIO scaffolds was greater than that in PU/PEO and PU/PEO/SPIO scaffolds, confirming the better compatibility of gelatin vs PEO as the viscosity enhancer of the ink. The gradual release of SPIO NPs from the scaffolds promoted the osteogenesis of seeded hMSCs. With SPIO in the scaffolds, the osteogenesis increased 2.7 times for PU/PEO and 1.5 times for PU/gelatin scaffolds based on the collagen content. Meanwhile, SPIO release from PU/PEO/SPIO scaffolds was faster than that from PU/gelatin/SPIO scaffolds at 14 days, consistent with the better osteogenesis observed in PU/PEO/SPIO scaffolds. We concluded that 3D printed PU scaffolds with shape memory properties, biodegradability, and osteogenic effect may be employed to the minimally invasive surgical procedures as customized-bone substitutes for bone tissue engineering

Functionalized Nanoporous Gyroid SiO₂ with Double-Stimuli-Responsive Properties as Environment-Selective Delivery Systems

Herein, we aim to fabricate nanoporous gyroid SiO₂ from templated sol–gel reaction using degradable block copolymer with gyroid-forming nanostructure as a template and then to functionalize the nanoporous materials using “smart” polymer, poly­(2-(dimethylamino)­ethyl methacrylate) (PDMAEMA), brushes via the “grafting from” method to give double-stimuli-responsive properties. By taking advantage of the responses to environmental stimuli, both thermal and pH, the pore features can be well-defined by the stretching and recoiling of PDMAEMA brushes because of their adjustable chain conformations with reversible character. The responsive properties with respect to environmental stimuli can be successfully traced by temperature-resolved small-angle X-ray scattering (SAXS) in aqueous environment. Owing to the high specific surface area and porosity, 3D pore network, biocompatibility, and environmental responses, the functionalized nanoporous gyroid SiO₂ is further demonstrated as a stimuli-responsive controlled release system