Gelatin Methacryloyl–Riboflavin (GelMA–RF) Hydrogels for Bone Regeneration

Gelatin methacryloyl (GelMA) is a versatile biomaterial that has been used in various biomedical fields. UV light is commonly used to photocrosslink such materials; however, its use has raised several biosafety concerns. We investigated the mechanical and biological properties of a visible-wavelength (VW)-light-crosslinked gelatin-based hydrogel to evaluate its viability as a scaffold for bone regeneration in bone-destructive disease treatment. Irgacure2959 or riboflavin was added as a photoinitiator to create GelMA solutions. GelMA solutions were poured into a mold and exposed to either UV or VW light. KUSA-A1 cell-laden GelMA hydrogels were crosslinked and then cultured. Mechanical characterization revealed that the stiffness range of GelMA–RF hydrogel was suitable for osteoblast differentiation. KUSA-A1 cells encapsulated in GelMA hydrogels photopolymerized with VW light displayed significantly higher cell viability than cells encapsulated in hydrogels photopolymerized with UV light. We also show that the expression of osteogenesis-related genes at a late stage of osteoblast differentiation in osteoblasts encapsulated in GelMA–RF hydrogel was markedly increased under osteoblast differentiation-inducing conditions. The GelMA–RF hydrogel served as an excellent scaffold for the encapsulation of osteoblasts. GelMA–RF hydrogel-encapsulated osteoblasts have the potential not only to help regenerate bone mass but also to treat complex bone defects associated with bone-destructive diseases such as periodontitis.     

Photoswitchable Sn‐Cyt c Solid‐State Devices

Electron transfer across proteins plays an important role in many biological processes, including those relevant for the conversion of solar photons to chemical energy. Previous studies demonstrated the generation of photocurrents upon light irradiation in a number of photoactive proteins, such as photosystem I or bacteriorhodopsin. Here, it is shown that Sn‐cytochrome c layers act as reversible and efficient photoelectrochemical switches upon integration into large‐area solid‐state junctions. Photocurrents are observed both in the Soret band (λ = 405 nm) and in the Q band (λ = 535 nm), with current on/off ratios reaching values of up to 25. The underlying modulation in charge‐transfer rate is attributed to a hole‐transport channel created by the photoexcitation of the Sn‐porphyrin.     

Influences of the ZrC coating process and heat treatment on ZrC-coated kernels used as fuel in Pu-burner high temperature gas-cooled reactor in Japan

ABSTRACT

The concept of Pu-burner high temperature gas-cooled reactor (HTGR) has been proposed to more safely reduce the amount of recovered Pu. In the Pu-burner HTGR concept, coated fuel particles with ZrC-coated yttria-stabilized zirconia containing PuO₂ (PuO₂-YSZ) kernels are employed for very high burn-up and high nuclear proliferation resistance. The role of ZrC layer is that of oxygen getter. CeO₂-YSZ kernels were fabricated to simulate the PuO₂-YSZ kernel and coated with a ZrC layer. In this study, we clarified that both Ce-rich grains and Zr-rich grains were densely distributed in surface regions of the as-fabricated CeO₂-YSZ kernel. However, we have already clarified that the surface region of the CeO₂-YSZ kernel coated with a ZrC layer was porous and mainly consisted of Zr-rich grains. These experimental results confirmed that Ce-rich grains were selectively corroded during the ZrC coating process. Then, the chemical stability of Zr-rich grains would be higher than that of Pu-rich grains. Thus, it would be more difficult to extract Pu from PuO₂-YSZ kernels (in which almost all grains are Zr-rich) than from PuO₂-YSZ kernels (in which many Pu-rich grains are included). Influences of the sintering of fuel compact on the microstructure of the ZrC-coated CeO₂-YSZ kernel is also reported.     

Helical twisting power of three-ring chiral molecules and polymerization in cholesteric electrolyte solutions

A series of chiral three-ring type compounds with rigid shape was employed as chiral inducers for induction of chiral cholesteric liquid crystal (cholesteric LC) from achiral nematic LC. Helical twisting power of the chiral compounds was estimated with the Cano wedge method. Cholesteric LC electrolyte solution was prepared by adding the chiral compounds. Subsequently, polymerization in the cholesteric LC was carried out to produce chiroptically active polymer films. This method is different from conventional methods for synthesizing chiral polymers because neither chiral monomers nor asymmetric catalysts are employed. Surface structure and optical properties of the polymer thus prepared were examined.     

Fabrication of transparent SiO2 glass by pressureless sintering and spark plasma sintering

Transparent SiO₂ bodies were prepared by pressureless sintering (PLS) and spark plasma sintering (SPS). The effects of sintering and annealing temperature on the transmittance of the SiO₂ bodies were investigated. The SiO₂ bodies sintered by SPS and PLS at 1073–1573 K were amorphous. With increasing the sintering temperature to 1673 K, the SiO₂ bodies sintered by PLS were crystallized while those sintered by SPS were still amorphous. The relative density of the SiO₂ bodies sintered by SPS was 98.5% at 1373 K and 100% at 1573 K, whereas that sintered by PLS was 92.6% at 1373 K and 98.9% at 1573 K. The transmittance was 91.0% and 81.5% at a wavelength (λ) of 2 μm for the SiO₂ sintered bodies by SPS and PLS, respectively. In the ultraviolet range, the transmittance of the SiO₂ bodies sintered by SPS at 1573 K was about 40% at λ = 200 nm and increased to 75% after annealing at 1073 K for 1 h, which was about three times of the transmittance of the SiO₂ bodies sintered by PLS (24.8%).     

Effect of calcination temperature on the fabrication of transparent lutetium titanate by spark plasma sintering

Transparent lutetium titanate (Lu₂Ti₂O₇) bodies were fabricated by spark plasma sintering using Lu₂O₃ and TiO₂ powders calcined from 700 °C to 1200 °C. No solid-state reaction was identified after calcination at 700 °C, whereas single-phase Lu₂Ti₂O₇ powder was prepared at 1100 and 1200 °C. The calcination at 700 °C promoted densification at the early stages of sintering, whereas residual pores at grain boundaries resulted in Lu₂Ti₂O₇ bodies with low transparency. Low-density and opaque Lu₂Ti₂O₇ bodies formed owing to the coarsening of the powder calcined at 1200 °C. The Lu₂Ti₂O₇ body sintered using the powder calcined at the moderate temperature of 1100 °C had a density of 99.5% with the highest transmittances of 41% and 74% at wavelengths of 550 nm and 2000 nm, respectively.     

Gold nanorods in an oil-base formulation for transdermal treatment of type 1 diabetes in mice

Efficient transdermal insulin delivery to the systemic circulation would bring major benefit to diabetic patients. We investigated the possibility of using gold nanorods (GNRs) that formed a complex with an edible surfactant and insulin (INS) in an oil phase to form a solid-in-oil (SO) formulation (SO-INS-GNR) for transdermal treatment of diabetes. Diabetic mice comprised the model for our study. In vitro, there was high penetration of insulin through the stratum corneum (SC) and the dermis in mouse skin treated with an SO-INS-GNR complex plus near-infrared (NIR) light irradiation. Blood glucose levels in the diabetic mice were significantly decreased after treatment with SO-INS-GNR plus irradiation. To our knowledge, this is the first study to use gold nanorods for systemic insulin delivery through the skin. The use of an SO-INS-GNR complex combined with NIR irradiation may provide the possibility of transdermal insulin delivery to diabetic patients.