Composite ceramics enhance cell colonization in bone applications, indicating potential for tissue engineering.
Via a solid-state reaction route, magnetic composites of chicken eggshell-derived β -tricalcium phosphate ( β -TCP, referred to as TCP in the composite system) and zinc-nickel spinel ferrite (ZNF; Zn x Ni 1‒ x Fe 2 O 4 , x = 0.2, 0.4, 0.6, or 0.8) were successfully fabricated. Discs were prepared by uniaxial pressing of milled ZNF/TCP powders and sintered at 1200 °C. Cytocompatibility of all composites was confirmed by SEM observations of human osteoblasts (h-OBs) and MTT assays. At 4-wt% ZNF addition, the composites containing Zn 0.8 Ni 0.2 Fe 2 O 4 (Z8NF) exhibited the greatest extent of early cell spreading and were selected for further investigation. For Z8NF/TCP composites containing 4–12 wt% Z8NF, the 8–12 wt% samples demonstrated the highest levels of cell colonization, while MTT assays suggested non-cytotoxic behavior, with cell viabilities comparable to β -TCP. High-temperature sintering induced partial transformation of β -TCP to β -calcium pyrophosphate ( β -CPP), as evidenced by XRD and Rietveld refinement. Increasing Z8NF content promoted β -CPP formation and increased composite porosity, whereas densification and Vickers hardness decreased accordingly. Rietveld refinement further indicated that the detectable crystalline Z8NF phase persisted as a minor yet stable secondary phase ( < 2 wt%) and did not participate in Ca–P lattice substitution. For the 8–12 wt% composites, saturation magnetization decreased with increasing Z8NF because of higher porosity and dilution by the non-magnetic β -TCP/ β -CPP matrix, while coercivity increased owing to enhanced effective magnetic anisotropy in the more porous microstructure. Overall, the Z8NF/TCP composites combined biodegradability, bioactivity, and tunable soft-magnetic properties, suggesting their potential for bone repair and bone tissue engineering applications.
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Pankaew et al. (2026) studied this question.
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