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The applications of a variety of bioactive ceramics such as hydroxyapatite (HA) in orthopedics are limited by their insufficient mechanical properties, especially poor fracture toughness. Thus, further extending the clinical applications of these materials warrants the enhancement of their mechanical properties. Although the reinforcement of ceramics by 2D nanomaterials has been well recognized, integrated structural, mechanical, and functional considerations have been neglected in the design and synthesis of such composite materials. Herein, we report the first use of silica-coated reduced graphene oxide (S-rGO) hybrid nanosheets to create bioceramic-based composites with simultaneously enhanced mechanical and biological properties. In the representative HA-based bioceramic systems prepared by spark plasma sintering, S-rGO incorporation was found to be more effective for increasing the Young's modulus, hardness, and fracture toughness than the incorporation of uncoated reduced GO (rGO). Furthermore, when assessed with osteoblast-like MG-63 cells, such novel materials led to faster cell proliferation and higher cell viability and alkaline phosphatase activity than are generally observed with pure HA; additionally, cells demonstrate stronger affinity to S-rGO/HA than to rGO/HA composites. The S-rGO/bioceramic composites are therefore promising for applications in orthopedic tissue engineering, and this research provides valuable insights into the fabrication of silica-coated hybrid nanosheet-reinforced ceramics. Nanyang Technological University This study was supported by Nanyang Technological University (NTU,Grant No. M4080160).

A copolyester was prepared from p-hydroxybenzoic acid (HBA), 2,6-naphthalene dicaboxylic acid (NDA), and hydroquinone (HQ). Thermal transition behavior and the crystal structure of this copolyester were investigated by using polarized light microscopy (PLM), differential scanning calorimetry (DSC), and wide-angle X-ray diffraction (WAXD) after annealing at solid-phase polymerization conditions. A glass transition or newly ordered structure in the 270-290°C range was observed on annealing at 260°C, which increased with annealing time, attributed to mobility and reactive rearrangement in amorphous regions. Broad and unclear WAXD profiles and multimelting behaviors were found on annealing at 280°C, and explained by hexagonal and orthorhombic lattice formation and transformation. A large increase in melting temperature was observed only on annealing at a temperature (320°C) near the crystal-nematic transition, suggesting annealing temperatures near the melting point are required for sufficient mobility to afford crystalline rearrangement via transesterification.