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The inclusion of zinc into mineralized collagen scaffolds for craniofacial bone repair applications.
Tiffany, Aleczandria S; Gray, Danielle L; Woods, Toby J; Subedi, Kiran; Harley, Brendan A C.
Affiliation
  • Tiffany AS; Dept. Chemical and Biomolecular Engineering, University of Illinois at Urbana-Champaign, Urbana, IL 61801, United States.
  • Gray DL; School of Chemical Sciences, University of Illinois at Urbana-Champaign, Urbana, IL 61801, United States.
  • Woods TJ; School of Chemical Sciences, University of Illinois at Urbana-Champaign, Urbana, IL 61801, United States.
  • Subedi K; School of Chemical Sciences, University of Illinois at Urbana-Champaign, Urbana, IL 61801, United States.
  • Harley BAC; Dept. Chemical and Biomolecular Engineering, University of Illinois at Urbana-Champaign, Urbana, IL 61801, United States; Carl R. Woese Institute for Genomic Biology, University of Illinois at Urbana-Champaign, Urbana, IL 61801, United States. Electronic address: bharley@illinois.edu.
Acta Biomater ; 93: 86-96, 2019 07 15.
Article in En | MEDLINE | ID: mdl-31121312
ABSTRACT
Implant osteoinduction and subsequent osteogenic activity are critical events that need improvement for regenerative healing of large craniofacial bone defects. Here we describe the augmentation of the mineral content of a class of mineralized collagen scaffolds under development for craniomaxillofacial bone regeneration via the inclusion of zinc ions to promote osteogenesis in vitro. Zinc is an essential trace element in skeletal tissue and bone, with soluble zinc being shown to promote osteogenic differentiation of porcine adipose derived stem cells. We report the development of a new class of zinc functionalized scaffolds fabricated by adding zinc sulfate to a mineralized collagen-glycosaminoglycan precursor suspension that was then freeze dried to form a porous biomaterial. We report analysis of zinc functionalized scaffolds via imaging (scanning electron microscopy), mechanical testing (compression), and compositional (X-ray diffraction, inductively coupled plasma mass spectrometry) analyses. Notably, zinc-functionalized scaffolds display morphological changes to the mineral phase and altered elastic modulus without substantially altering the composition of the brushite phase or removing the micro-scale pore morphology of the scaffold. These scaffolds also display zinc release kinetics on the order of days to weeks and promote successful growth and pro-osteogenic capacity of porcine adipose derived stem cells cultured within these zinc scaffolds. Taken together, we believe that zinc functionalized scaffolds provide a unique platform to explore strategies to improve in vivo osteogenesis in craniomaxillofacial bone injuries models. STATEMENT OF

SIGNIFICANCE:

Craniomaxillofacial bone defects that arise from traumatic, congenital, and post-oncologic origins cannot heal on their own and often require surgical intervention. We have developed a class of mineralized collagen scaffolds that promotes osteogenesis and bone regeneration. Here we describe the inclusion of zinc sulfate into the mineralized collagen scaffold to improve osteogenesis. Zinc functionalized scaffolds demonstrate altered crystallite microstructure but consistent Brushite chemistry, improved mechanics, and promote zinc transporter expression while supporting stem cell viability, osteogenic differentiation, and mineral biosynthesis.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Zinc / Bone Regeneration / Calcification, Physiologic / Adipose Tissue / Collagen / Tissue Scaffolds / Mesenchymal Stem Cells Limits: Animals Language: En Journal: Acta Biomater Year: 2019 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Zinc / Bone Regeneration / Calcification, Physiologic / Adipose Tissue / Collagen / Tissue Scaffolds / Mesenchymal Stem Cells Limits: Animals Language: En Journal: Acta Biomater Year: 2019 Document type: Article Affiliation country: