posted on 2017-10-11, 00:00authored byJiayi Yu, Yanyi Xu, Shan Li, Gabrielle V. Seifert, Matthew L. Becker
Polymer–bioceramic
composites incorporate the desirable
properties of each material while mitigating the limiting characteristics
of each component. 1,6-Hexanediol l-phenylalanine-based poly(ester
urea) (PEU) blended with hydroxyapatite (HA) nanocrystals were three-dimensional
(3D) printed into porous scaffolds (75% porosity) via fused deposition
modeling and seeded with MC3T3-E1 preosteoblast cells in vitro to
examine their bioactivity. The resulting 3D printed scaffolds exhibited
a compressive modulus of ∼50 MPa after a 1-week incubation
in PBS at 37 °C, cell viability >95%, and a composition-dependent
enhancement of radio-contrast. The influence of HA on MC3T3-E1 proliferation
and differentiation was measured using quantitative real-time polymerase
chain reaction, immunohistochemistry and biochemical assays. After
4 weeks, alkaline phosphatase activity increased significantly for
the 30% HA composite with values reaching 2.5-fold greater than the
control. Bone sialoprotein showed approximately 880-fold higher expression
and 15-fold higher expression of osteocalcin on the 30% HA composite
compared to those of the control. Calcium quantification results demonstrated
a 185-fold increase of calcium concentration in mineralized extracellular
matrix deposition after 4 weeks of cell culture in samples with higher
HA content. 3D printed HA-containing PEU composites promote bone regeneration
and have the potential to be used in orthopedic applications.