Biodegradable-Glass-Fiber Reinforced Hydrogel Composite with Enhanced Mechanical Performance and Cell Proliferation for Potential Cartilage Repair.

Polyvinyl alcohol (PVA) hydrogels are promising implants due to the similarity of their low-friction behavior to that of cartilage tissue, and also due to their non-cytotoxicity. However, their poor mechanical resistance and insufficient durability restricts their application in this area. With the development of biodegradable glass fibers (BGF), which show desirable mechanical performance and bioactivity for orthopedic engineering, we designed a novel PVA hydrogel composite reinforced with biodegradable glass fibers, intended for use in artificial cartilage repair with its excellent cytocompatibility and long-term mechanical stability. Using structure characterization and thermal properties analysis, we found hydrogen bonding occurred among PVA molecular networks as well as in the PVA-BGF interface, which explained the increase in crystallinity and glass transition temperature, and was the reason for the improved mechanical performance and better anti-fatigue behavior of the composites in comparison with PVA. The compressive strength and modulus for the PBGF-15 composite reached 3.05 and 3.97 MPa, respectively, equaling the mechanical properties of human articular cartilage. Moreover, the increase in BGF content was found to support the proliferation of chondrocytes in vitro, whilst the PVA hydrogel matrix was able to control the ion concentration by adjusting the ions released from the BGF. Therefore, this novel biodegradable-glass-fiber-reinforced hydrogel composite possesses excellent properties for cartilage repair with potential in medical application.

Production and characterisation of novel phosphate glass fibre yarns, textiles, and textile composites for biomedical applications.

This work presents manufacturing, processing and characterisation of the phosphate glass fibre (PGF) products for biomedical applications, including multifilament PGF strands, yarns and textiles, and PGF textile composites. The multifilament production of PGF strands was achieved using a 50-nozzle bushing. PGF yarns, with a linear density of 87 tex, a twist angle of 14° and a tensile strength of 0.29 N/tex, were produced by combining 8 fibre strands using the ring-spinning method. PGF textiles, with a width of 15 mm and a thickness of 0.36 mm, were prepared using an inkle loom. The maximum flexural strength and modulus of unidirectional (UD) composites with a fibre volume fraction of ~17% were 262 ±â€¯11 MPa and 10.4 ±â€¯0.2 GPa, respectively. PGF textile composites with a fibre volume fraction of ~21% exhibited mechanical properties of 176 ±â€¯13 MPa for flexural strength and 8.6 ±â€¯0.6 GPa for flexural modulus. Despite the UD and textile composites having almost an equivalent amount of fibres in the 0 direction, the crimp of the yarns was found to contribute to the significantly lower flexural properties of the textile composites in comparison with the unidirectional (UD) composites. Additionally, the processing conditions such as processing temperature and time were found to have a strong effect on the mechanical properties of the resultant composite products. The number-average molecular weight of PLA was also found to reduce by 13% and 19% after the production of PLA films and PLA plates, respectively, in comparison with the as-received PLA pellets.