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)研究チームは、再生促進する3Dプリント可能生体材料足場(スキャフォールド)開発した。材料生体適合ポリマーミネラル成分組み合わせ、組織迅速成長できる多孔構造形成する。3Dプリントにより患者損傷部位合わせ形状足場作製でき、細胞付着増殖促進する設計っている。実験では細胞成長効率支えること確認れ、骨折欠損治療、組織工学、再生医療応用期待れる。研究将来に、個別医療対応した再生治療発展寄与する可能性ある。

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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