Porous polymer scaffolds designed by the cryogel method are attractive materials for a range of tissue engineering applications. However, the use of toxic cross-linker for retaining the pore structure limits their clinical applications. In this research, acrylates (HEA/PEGDA, HEMA/PEGDA and PEGDA) were used in the low-temperature soli d-state photopolymerization to produce porous scaffolds with good structural retention. The morphology, pore diameter, mineral deposition and water absorption of the scaffold were characterized by SEM and water absorption test respectively. Elemental analysis and cytotoxicity of the biomineralized scaffold were revealed by using XRD and MTT assay test. The PEGDA-derived scaffold showed good water absorption ability and a higher degree of porosity with larger pore size compared to others. XRD patterns and IR results confirmed the formation of hydroxyapatite crystals from an alternative socking process. The overall cell proliferation was excellent, where PEGDA-derived scaffold had the highest and the most uniform cell growth, while HEMA/PEGDA scaffold showed the least. These results suggest that the cell proliferation and adhesion are directly proportional to the pore size, the shape and the porosity of scaffolds.

Titanium (Ti) implants with TiO₂ nanotubular arrays on the surface could regulate cells adhesion, proliferation and differentiation to determine the bone integration. Additionally, the regulation of immune cells could improve osteogenesis or lead in appropriate immune reaction. Thus, we evaluate the behavior of RAW 264.7 macrophages on TiO₂ nanotubular arrays with a wide range diameter (from 20 to 120 nm) fabricated by an electrochemical anodization process. In this work, the proliferation, cell viability and cytokine/chemokine secretion were evaluated by CCK-8, live/dead staining and ELISA, respectively. SEM and confocal microscopy were used to observe the adhesion morphology. Results showed that the small size nanotube surface was benefit for the macrophages adhesion and proliferation, while larger size surface could reduce the inflammatory response. These findings contribute to the design of immune-regulating Ti implants surface that supports successful implantation.

A novel type of amphiphilic pH-responsive folate-poly(ε-caprolactone)-block-poly(2-hydroxyethylmethacrylate)-co-poly(2-(dimethylamino)-ethylmethacrylate) (FA-PCL-b-P(HEMA-co-DMAEMA)) (MFP) block copolymers were designed and synthesized via atom transfer radical polymerization (ATRP) and ring opening polymerization (ROP) techniques. The molecular structures of the copolymers were confirmed with¹H NMR, FTIR and GPC measurements. The critical micelle concentration (CMC) of MFP in aqueous solution was extremely low (about 6.54 mg/L). Thein vitro release behavior of DOX-loaded micelles was significantly accelerated when the pH value of solution decreased from 7.4 to 5.0. In vitro antitumor efficiency was evaluated by incubating DOX- loaded micelles with Hela cells. The results demonstrated that this copolymer possessed excellent biocompatibility, and FA-decorated micelles MFP showed higher cellular uptake than those micelles without the FA moiety, indicating their unique targetability. These folate-conjugated biodegradable micelles are highly promising for targeted cancer chemothe-rapy.

Ga₂O₃ was doped into 0.95(K_0.48Na_0.52)NbO₃–0.05LiTaO₃ (KNN–LT) ceramics and its influences on the sintering behavior, phase structure and electrical properties of ceramics were studied. Firstly, SEM observation exhibits that more and more glass phase appears in ceramics with the gradual addition of Ga₂O₃, which determines the continuous decrease in sintering temperatures. And the addition of Ga₂O₃ is also found to increase the orthorhombic–tetragonal transition temperature (T_O–T) of system to a higher level. Secondly, both the density and the coercive?field (E_C) of ceramics increase firstly and then decrease with increasing the Ga₂O₃ content, and the KNN–LT–xGa sample at x = 0.004 shows a pinched P–E hysteresis loop. Finally, the impedance characteristics of KNN–LT–xGa ceramics were investigated at different temperatures, revealing a typical vacancy related conduction mechanism. This work demonstrates that Ga₂O₃ is a good sintering aid for KNN-based ceramics, and the vacancy plays an important role in the sintering and electrical behaviors of ceramics.

Chain-like zircona (ZrO₂) nanofibers were prepared by microwave sintering without any surfactants or solid templates. Microwave sintering was conducted in a multimode microwave cavity with TE666 resonant mode at 2.45 GHz. Carbon particles were used to activate unique thermal processes when mixed with ZrO₂ precursor. The sintering condition was at 1300°C for 10 min. Samples were characterized by XRD, SEM, TEM techniques. It was found that both monolithic and tetragonal ZrO₂ co-existed in samples prepared from the mixture of ZrO₂ precursors and carbon by either microwave or conventional sintering. Only m-ZrO₂ exists in samples prepared by ZrO₂ precursors without carbon. ZrO₂ appeared as chain-like nanofibers, which might be attributed to a so-called carbon-induced self-assembly growth mechanism.

Anatase TiO₂ with a variant percentage of exposed (001) facets was prepared under hydrothermal processes by adjusting the volume of HF, and the photocatalytic mechanism was studied from atomic-molecular scale by HRTEM and Raman spectroscopy. It was revealed that: 1) From HRTEM observations, the surface of original TiO₂ with exposed (001) facets was clean without impurity, and the crystal lattice was clear and completed; however, when mixed with methylene blue (MB) solution, there were many 1 nm molecular absorbed at the surface of TiO₂; after the photocatalytic experiment, MB molecules disappeared and the TiO₂ lattice image became fuzzy. 2) The broken path of the MB chemical bond was obtained by Raman spectroscopy, i.e., after the irradiation of the light, the vibrational mode of C−N−C disappeared due to the chemical bond breakage, and the groups containing C−N bond and carbon rings were gradually decomposed. Accordingly, we propose that the driving force for breaking the chemical bond and the disappearance of groups is from the surface lattice distortion of TiO₂ during photocatalyzation.

Highly efficient Ag₃PO₄/MoS₂ nanocomposite photocatalyst was synthesized using a wet chemical route with a low weight percentage of highly exfoliated MoS₂ (0.1 wt.%) and monodispersed Ag₃PO₄ nanoparticles (~5.4 nm). The structural and optical properties of the nanocomposite were studied using various characterization techniques, such as XRD, TEM, Raman and absorption spectroscopy. The composite exhibits markedly enhanced photocatalytic activity with a low lamp power (60 W). Using this composite, a high kinetic rate constant (k) value of 0.244 min⁻¹ was found. It was observed that ~97.6% of dye degrade over the surface of nanocomposite catalyst within 15 min of illumination. The improved photocatalytic activity of Ag₃PO₄/MoS₂ nanocomposite is attributed to the efficient interfacial charge separation, which was supported by the PL results. Large surface area of MoS₂ nanosheets incorporated with well dispersed Ag₃PO₄ nanoparticles further increases charge separation, contributing to enhanced degradation efficiency. A possible mechanism for charge separation is also discussed.

In the present study, novel Co₃O₄/NiO nanosponges designed for the photocatalytic degradation of organic contaminants were synthesized by a simple precipitation technique. The formation of sponge-like nanostructures was clearly evident through the TEM analysis. The photocatalytic efficiency was tested against rhodamine B (RhB) and congo red (CR) dye solutions. Co₃O₄/NiO nanosponges showed excellent and enhanced photocatalytic efficacy compared to those of Co₃O₄, NiO nanoparticles, and standards like TiO₂ and ZnO. The influence of paramount important operational parameters was explored and the conditions for the best photocatalytic efficiency were optimized. The trapping experiment revealed that the reactive oxygen species (ROS) identified was ·OH radical. These findings certainly open up a new way for synthesizing a morphology dependent photocatalyst.

Synthesis of nanostructured Ru-doped SnO₂ was successfully carried out using the reverse microemulsion method. The phase purity and the crystallite size were analyzed by XRD. The surface morphology and the microstructure of synthesized nanoparticles were analyzed by SEM and TEM. The vibration mode of nanoparticles was investigated using FTIR and Raman studies. The electrochemical behavior of the Ru-doped SnO₂ electrode was evaluated in a 0.1 mol/L Na₂SO₄ solution using cyclic voltammetry. The 5% Ru-doped SnO₂ electrode exhibited a high specific capacitance of 535.6 F/g at a scan rate 20 mV/s, possessing good conductivity as well as the electro-cycling stability. The Ru-doped SnO₂ composite shows excellent electrochemical properties, suggesting that this composite is a promising material for supercapacitors.

The present work demonstrates the possibilities of hydrothermal transformation of Zn–Al layered double hydroxide (LDH) nanostructure by varying the synthetic conditions. The manipulation in washing step before hydrothermal treatment allows control over crystal morphologies, size and stability of their aqueous solutions. We examined the crystal growth process in the presence and the absence of extra ions during hydrothermal treatment and its dependence on the drug (diclofenac sodium (Dic-Na)) loading and release processes. Hexagonal plate-like crystals show sustained release with ~90% of the drug from the matrix in a week, suggesting the applicability of LDH nanohybrids in sustained drug delivery systems. The fits to the release kinetics data indicated the drug release as a diffusion-controlled release process. LDH with rod-like morphology shows excellent colloidal stability in aqueous suspension, as studied by photon correlation spectroscopy.