4.8 Article

Versatile effects of magnesium hydroxide nanoparticles in PLGA scaffold-mediated chondrogenesis

期刊

ACTA BIOMATERIALIA
卷 73, 期 -, 页码 204-216

出版社

ELSEVIER SCI LTD
DOI: 10.1016/j.actbio.2018.04.022

关键词

Magnesium hydroxide; Chondrogenesis; Calcification; Cell death; Inflammation

资金

  1. Basic Science Research Program through the National Research Foundation of Korea - Ministry of Science and ICT (MSIT) [2017R1A2B3011121]
  2. Immune Mechanism Regulation Program through the National Research Foundation of Korea - Ministry of Science and ICT (MSIT) [2014M3A9D3033887]
  3. Core Materials Technology Development Program - Ministry of Trade, Industry and Energy (MOTIE), Republic of Korea [10048019]
  4. Materials and Components Technology Development Program - Ministry of Trade, Industry and Energy (MOTIE), Republic of Korea [10062079]
  5. Korea Evaluation Institute of Industrial Technology (KEIT) [10062079] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)
  6. National Research Foundation of Korea [2014M3A9D3033887, 2017R1A2B3011121] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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Artificial scaffolds made up of various synthetic biodegradable polymers have been reported to have many advantages including cheap manufacturing, easy scale up, high mechanical strength, convenient manipulation, and molding into an unlimited variety of shapes. However, the synthetic biodegradable polymers still have the insufficiency for cartilage regeneration owing to their acidic degradation products. To reduce acidification by degradation of synthetic polymers, we incorporated magnesium hydroxide (MH) nanoparticles into porous polymer scaffold not only to effectively neutralize the acidic hydrolysate but also to minimize the structural disturbance of scaffolds. The neutralization effect of poly(D,L-lactic-co-glycolic acid; PLGA)/MH scaffold was confirmed with the maintenance of neutral pH, contrary to a PLGA scaffold with low pH. Further, the scaffolds were applied to evaluate the chondrogenic differentiation of the human bone marrow mesenchymal stem cells. In in vitro study, the PLGA/MH scaffold enhanced the chondrogenesis markers and reduced the calcification, compared to the PLGA scaffold. Additionally, the PLGA/MH scaffold reduced the release of inflammatory cytokines, compared to the PLGA scaffold, as the cell death decreased. Moreover, the addition of MH reduced necrotic cell death at the early stage of chondrogenic differentiation. Further, the necrotic cell death by the PLGA scaffold was mediated by cleavage of caspase-1, the so-called interleukin 1-converting enzyme, and MH alleviated it as well as nuclear factor kappa B expression. Furthermore, the PLGA/MH scaffold highly supported chondrogenic healing of rat osteochondral defect sites in in vivo study. Therefore, it was suggested that a synthetic polymer scaffold containing MH could be a novel healing tool to support cartilage regeneration and further treatment of orthopedic patients. (C) 2018 Acta Materialia Inc. Published by Elsevier Ltd. All rights reserved.

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