3D Printing of Bone‐Mimetic Scaffold Composed of Gelatin/β‐Tri‐Calcium Phosphate for Bone Tissue Engineering

3D printed scaffolds composed of gelatin and β‐tri‐calcium phosphate (β‐TCP) as a biomimetic bone material are fabricated, thereby providing an environment appropriate for bone regeneration. The Ca2+ in β‐TCP and COO− in gelatin form a stable electrostatic interaction, and the composite scaffold sho...

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Veröffentlicht in:Macromolecular bioscience 2020-12, Vol.20 (12), p.e2000256-n/a
Hauptverfasser: Jeong, Jae Eun, Park, Shin Young, Shin, Ji Youn, Seok, Ji Min, Byun, June Ho, Oh, Se Heang, Kim, Wan Doo, Lee, Jun Hee, Park, Won Ho, Park, Su A
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Sprache:eng
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Zusammenfassung:3D printed scaffolds composed of gelatin and β‐tri‐calcium phosphate (β‐TCP) as a biomimetic bone material are fabricated, thereby providing an environment appropriate for bone regeneration. The Ca2+ in β‐TCP and COO− in gelatin form a stable electrostatic interaction, and the composite scaffold shows suitable rheological properties for bioprinting. The gelatin/β‐TCP scaffold is crosslinked with glutaraldehyde vapor and unreacted aldehyde groups which can cause toxicity to cells is removed by a glycine washing. The stable binding of the hydrogel is revealed as a result of FTIR and degradation rate. It is confirmed that the composite scaffold has compressive strength similar to that of cancellous bone and 60 wt% β‐TCP groups containing 40 wt% gelatin have good cellular activity with preosteoblasts. Also, in the animal experiments, the gelatin/β‐TCP scaffold confirms to induce bone formation without any inflammatory responses. This study suggests that these fabricated scaffolds can serve as a potential bone substitute for bone regeneration. 3D printed scaffolds are fabricated using collagen‐hydrolyzed gelatin and β‐tri‐calcium phosphate (β‐TCP) to mimetic bone tissue of collagenous network and calcium phosphate. The results show that the composite scaffold has a compressive strength similar to that of cancellous bone, good cellular activity, and induced bone formation without any inflammatory responses.
ISSN:1616-5187
1616-5195
DOI:10.1002/mabi.202000256