4.5 Article

Effect of pore architecture and stacking direction on mechanical properties of solid freeform fabrication-based scaffold for bone tissue engineering

期刊

JOURNAL OF BIOMEDICAL MATERIALS RESEARCH PART A
卷 100A, 期 7, 页码 1846-1853

出版社

WILEY
DOI: 10.1002/jbm.a.34149

关键词

scaffold; SFF technology; mechanical strength; pore architecture; stacking direction

资金

  1. National Research Foundation of Korea (NRF) [2011-0000412]
  2. Korea Government (MEST)
  3. Ministry of Health & Welfare, Republic of Korea
  4. contract grant number [A110416]
  5. Korea Health Promotion Institute [A110416] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

向作者/读者索取更多资源

Fabrication of a three-dimensional (3D) scaffold with increased mechanical strength may be an essential requirement for more advanced bone tissue engineering scaffolds. Various material- and chemical-based approaches have been explored to enhance the mechanical properties of engineered bone tissue scaffolds. In this study, the effects of pore architecture and stacking direction on the mechanical and cell proliferation properties of a scaffold were investigated. The 3D scaffold was prepared using solid freeform fabrication technology with a multihead deposition system. Various types of scaffolds with different pore architectures (lattice, stagger, and triangle types) and stacking directions (horizontal and vertical directions) were fabricated with a blend of polycaprolactone and poly lactic-co-glycolic acid. In compression tests, the triangle-type scaffold was the strongest among the experimental groups. Stacking direction affected the mechanical properties of scaffolds. An in vitro cell counting kit-8 assay showed no significant differences in optical density depending on the different pore architectures and stacking directions. In conclusion, mechanical properties of scaffolds can be enhanced by controlling pore architecture and stacking direction. (C) 2012 Wiley Periodicals, Inc. J Biomed Mater Res Part A, 2012.

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