The impact of multimodal pore size considered independently from porosity on mechanical performance and osteogenic behaviour of titanium scaffolds

Titanium porous scaffolds comprising multimodal pore ranges (i.e., uni-, bi-, tri-modal and random) were studied to evaluate the effect of pore size on osteoblastogenesis. The scaffolds were manufactured using spaceholderpowder metallurgy, and porosity and pore size were kept independent. Their mechanical and physical properties (i.e., stiffness, strength, total and open porosity) were determined. In a first step, unimodal porous samples were tested with a mouse osteoblastic clonal cell line to ascertain pore size and porosity effects on cellular behaviour. Their proliferation (via cell number and total protein content), differentiation (via ALP enzyme levels) and maturation potency (with gene markers (Runx2, osteocalcin) and cytoplasmatic calcium) were investigated. In a second step informed by the previous results, multimodal scaffolds were shortlisted according to a set of criteria that included stiffness similar to that of cortical or trabecular bone, high strength and high open porosity. Their bioactivity performance was then studied to assess the benefits of mixing different pore ranges. The study concludes that pre-osteoblasts cultivated in unimodal microstructures with a pore range 106?212 ?m of 36% total (actual) porosity and 300?500 ?m of 55% total (actual) porosity achieved the largest extent of maturation. Bimodal microstructures comprising small (106?212 ?m) and large (300?500 ?m) pore ranges, distinctively distributed within the volume, and 40% (actual) porosity outperformed others, including multimodal (i.e. three or more pore ranges) and non-porous samples. They displayed a synergistic effect over the unimodal distributions. This should be a consideration in the design of scaffolds for implantation and bioengineering applications.

Automated summary

Titanium porous scaffolds with different pore sizes were studied for their effects on osteoblastogenesis, with the conclusion that pore sizes of 106-212 µm and 300-500 µm achieved the best cell maturation effects, while bimodal structures with small and large pore sizes distributed distinctively and having 40% actual porosity outperformed others.