骨成長を高速化する3Dプリント足場材料を開発 (A 3D printable scaffold to support fast bone growth)

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2026-03-11 スイス連邦工科大学ローザンヌ校(EPFL)

スイス連邦工科大学ローザンヌ校(EPFL)の研究チームは、骨の再生を促進する3Dプリント可能な生体材料足場(スキャフォールド)を開発した。材料には生体適合性ポリマーとミネラル成分を組み合わせ、骨組織が迅速に成長できる多孔質構造を形成する。3Dプリントにより患者や損傷部位に合わせた形状の足場を作製でき、細胞の付着や増殖を促進する設計となっている。実験では骨細胞の成長を効率的に支えることが確認され、骨折や骨欠損の治療、組織工学、再生医療への応用が期待される。研究は将来的に、個別化医療に対応した骨再生治療の発展に寄与する可能性がある。

骨成長を高速化する3Dプリント足場材料を開発 (A 3D printable scaffold to support fast bone growth)
3D printing of scaffolds. (a) Enzyme-containing fragments are printed into a cylinder at room temperature in air (b) before being mineralized for 7 days (i, ii). (c) 3D printed Helicoprion shark tooth. 2026 EPFL SMaL CC BY SA

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酵素石灰化により形成された3Dプリント多孔質ハイドロキシアパタイト 3D-Printed Porous Hydroxyapatite Formed via Enzymatic Mineralization

Francesca Bono, Anna Puiggalí-Jou, Greta Cocchi, Mariangela Miccoli, Katharina Maniura-Weber, Marcy Zenobi-Wong, Esther Amstad
Advanced Functional Materials  Published: 27 February 2026
DOI:https://doi.org/10.1002/adfm.202526568

ABSTRACT

Bone combines mechanical resilience with low density and the ability to repair itself when damaged. Inspired by the fascinating density-normalized mechanical properties of bone, synthetic porous hydroxyapatite (HA)-based materials have been introduced. However, their production typically involves sintering, which is energy-intensive and restricts incorporation of biologically active components. Here, we introduce an enzyme-mediated strategy to 3D print HA-based composites that become load-bearing within 7 days of mineralization through an energy-efficient room-temperature process. This is achieved by embedding alkaline phosphatase in naturally derived hydrogel microfragments that are jammed to enable direct ink writing at room temperature. To control the porosity of the mineral-based composites, we include enzyme-free fragments. The resulting scaffolds exhibit compressive strengths of 3.65 MPa (5.5 MPa g1 cm3 specific strength) and low cytotoxicity. Through the introduction of open pores constituting up to 52 vol.% of the scaffold, we enable cells to infiltrate the scaffolds, thereby opening up new possibilities for cells to remodel them. We foresee the combination of mechanical performance, bioactivity, and energy-efficient processing to open new avenues for bone tissue engineering and mineral repair, where broken structures have the potential to bear significant loads much faster than currently available solutions do.

生物化学工学
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