4.8 Article

Biomaterials with structural hierarchy and controlled 3D nanotopography guide endogenous bone regeneration

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SCIENCE ADVANCES
卷 7, 期 31, 页码 -

出版社

AMER ASSOC ADVANCEMENT SCIENCE
DOI: 10.1126/sciadv.abg3089

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资金

  1. National Institute of General Medical Science (NIGMS) at the NIH [R01GM123081, R01GM138552, P30GM127200]
  2. National Institute of Dental and Craniofacial Research (NIDCR) at the NIH [1R21DE027516]
  3. Congressionally Directed Medical Research Program (CDMRP)/Peer Reviewed Medical Research Program (PRMRP) [FY19 W81XWH2010207, NE LB606]
  4. University of Nebraska Medical Center (UNMC)
  5. Nebraska Center for Nanomedicine (NCN) Center for Biomedical Research Excellence (Institutional Development Award, NIGMS of the NIH) [P30GM127200]
  6. Nebraska Research Initiative
  7. UNMC Office

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This study describes a class of 3D nanofiber scaffolds with hierarchical structure and controlled alignment for effective endogenous cranial bone regeneration. The radially aligned nanofibers in the scaffolds promoted the migration of bone marrow stem cells, resulting in the highest new bone volume, surface coverage, and mineral density among the tested groups in vivo. The regenerated bone exhibited a radially aligned fashion and showed a densely packed structure in the organic phase and a uniform distribution with smaller pore size in the inorganic mineral phase.
Biomaterials without exogenous cells or therapeutic agents often fail to achieve rapid endogenous bone regeneration with high quality. Here, we reported a class of three-dimensional (3D) nanofiber scaffolds with hierarchical structure and controlled alignment for effective endogenous cranial bone regeneration. 3D scaffolds consisting of radially aligned nanofibers guided and promoted the migration of bone marrow stem cells from the surrounding region to the center in vitro. These scaffolds showed the highest new bone volume, surface coverage, and mineral density among the tested groups in vivo. The regenerated bone exhibited a radially aligned fashion, closely recapitulating the scaffold's architecture. The organic phase in regenerated bone showed an aligned, layered, and densely packed structure, while the inorganic mineral phase showed a uniform distribution with smaller pore size and an even distribution of stress upon the simulated compression. We expect that this study will inspire the design of next-generation biomaterials for effective endogenous bone regeneration with desired quality.

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