4.8 Article

Biofunctionalized composite scaffold to potentiate osteoconduction, angiogenesis, and favorable metabolic microenvironment for osteonecrosis therapy

Journal

BIOACTIVE MATERIALS
Volume 9, Issue -, Pages 446-460

Publisher

KEAI PUBLISHING LTD
DOI: 10.1016/j.bioactmat.2021.08.005

Keywords

Biofunctionalized scaffold; Osteoconduction; Angiogenesis; Favorable metabolic microenvironment; Osteonecrosis therapy

Funding

  1. National Natural Science Foundation of China [52022095, 51973216, 51873207, 51803006, 51833010]
  2. Provincial Health Specific Project of Jilin Province [JLSWSRCZX2020-0021, 2018SCZ018, SCZSY201710]
  3. Specific Project for Health Research Talents of Jilin Province [2019SCZ025]
  4. Science and Technology Development Program of Jilin Province [20200404182YY, 20200201478JC, 20190303154SF]
  5. Youth Innovation Promotion Association of Chinese Academy of Sciences [2019230]
  6. State Key Laboratory of Advanced Technology for Materials Synthesis and Processing (Wuhan University of Technology) [2020-KF-5]

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This study developed a bio-functionalized composite scaffold for osteonecrosis therapy, which showed excellent performances in enhancing osteoconduction, angiogenesis, and a favorable metabolic microenvironment.
Osteonecrosis is a common orthopedic disease in clinic, resulting in joint collapse if no appropriate treatment is performed in time. Core decompression is a general treatment modality for early osteonecrosis. However, effective bone regeneration in the necrotic area is still a significant challenge. This study developed a bio-functionalized composite scaffold (PLGA/nHA(30)(VEGF)) for osteonecrosis therapy through potentiation of osteoconduction, angiogenesis, and a favorable metabolic microenvironment. The composite scaffold had a porosity of 87.7% and compressive strength of 8.9 MPa. PLGA/nHA(30)(VEGF) had an average pore size of 227.6 mu m and a water contact angle of 56.5 degrees with a sustained release profile of vascular endothelial growth factor (VEGF). After the implantation of PLGA/nHA(30)(VEGF), various osteogenic and angiogenic biomarkers were upregulated by 2-9 fold compared with no treatment. Additionally, the metabolomic and lipidomic profiling studies demonstrated that PLGA/nHA(30)(VEGF) effectively regulated the multiple metabolites and more than 20 inordinate metabolic pathways in osteonecrosis. The excellent performances reveal that the biofunctionalized composite scaffold provides an advanced adjuvant therapy modality for osteonecrosis.

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