4.5 Article

Design of a multiphase osteochondral scaffold. II. Fabrication of a mineralized collagen-glycosaminoglycan scaffold

Journal

JOURNAL OF BIOMEDICAL MATERIALS RESEARCH PART A
Volume 92A, Issue 3, Pages 1066-1077

Publisher

WILEY
DOI: 10.1002/jbm.a.32361

Keywords

bone; scaffold; collagen; regeneration

Funding

  1. Cambridge-MIT Institute
  2. Whitaker-MIT Health Science Fund Fellowship
  3. Matoula S. Salapatas Professorship at MIT
  4. Universities UK
  5. The Cambridge Commonwealth Trust
  6. St. John's College, Cambridge University

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This paper is the second in a series of papers describing the design and development of in osteochondral scaffold using collagen-glycosaminoglycan and calcium phosphate technologies engineered for the regenerative repair of articular cartilage defects. The previous paper described a technology (concurrent mapping) for systematic variation and control of the chemical composition of triple coprecipitated collagen, glycosaminoglycan and calcium phosphate (CGCaP) nanocomposites without Using titrants. This paper describes (1) fabricating porous, three-dimensional scaffolds from the CGCaP suspensions, (2) characterizing the microstructure and mechanical properties of such scaffolds, and (3) modifying the calcium phosphate mineral phase. The methods build on the previously, demonstrated ability to vary the composition of a CGCaP suspension (calcium phosphate mass fraction between 0 and 80 wt %) and enable the production of scaffolds whose pore architecture (mean pore size: 50-1000 mu m), CaP phase chemistry (brushite, octacalcium phosphate, apatite) and crosslinking density (therefore mechanical properties and degradation rate) can be independently controlled. The scaffolds described in this paper combine the desirable biochemical properties and pore architecture of porous collagen-glycosaminoglycan scaffolds with the strength and direct bone-bonding properties of calcium phosphate biomaterials in a manner that can be tailored to meet the demands of a range of applications in orthopedics and regenerative medicine. (C) 2009 Wiley Periodicals, Inc. J Biomed Mater Res 92A: 1066-1077, 2010

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