4.8 Article

MgAl layered double hydroxide/chitosan porous scaffolds loaded with PFTα to promote bone regeneration

期刊

NANOSCALE
卷 9, 期 20, 页码 6765-6776

出版社

ROYAL SOC CHEMISTRY
DOI: 10.1039/c7nr00601b

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资金

  1. Natural Science Foundation of China [51372152, 81472066]
  2. Innovation Foundation of Shanghai Education Committee [14ZZ124]
  3. Key Disciplines of Shanghai Municipal Education Commission [J50206]
  4. National High Technology Research and Development Program of China [2012AA020506]
  5. Priority Among Priorities Clinical Medical Centre Construction Project of the Shanghai Municipal, Science and Technology Commission of Shanghai Municipality [12JC1405600]

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Poor bone formation remains a key risk factor associated with acellular scaffolds that occurs in some bone defects, particularly in patients with metabolic bone disorders and local osteoporosis. We herein fabricated for the first time layered double hydroxide-chitosan porous scaffolds loaded with PFT alpha (LDH-CS-PFT alpha scaffolds) as therapeutic bone scaffolds for the controlled release of PFT alpha to enhance stem cell osteogenic differentiation and bone regeneration. The LDH-CS scaffolds had three-dimensional interconnected macropores, and plate-like LDH nanoparticles were uniformly dispersed within or on the CS films. The LDH-CS scaffolds exhibited appropriate PFT alpha drug delivery due to hydrogen bonding among LDH, CS and PFT alpha. In vitro functional studies demonstrated that the PFT alpha molecules exhibited potent ability to induce osteogenesis of hBMSCs via the GSK3 beta/beta-catenin pathway, and the LDH-CS-PFT alpha scaffolds significantly enhanced the osteogenic differentiation of hBMSCs. In vivo studies revealed significantly increased repair and regeneration of bone tissue in cranial defect model rats compared to control rats at 12 weeks post-implantation. In conclusion, the LDH-CS-PFT alpha scaffolds exhibited excellent osteogenic differentiation and bone regeneration capability and hold great potential for applications in defined local bone regeneration.

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