4.8 Article

Growth-Factor Free Multicomponent Nanocomposite Hydrogels That Stimulate Bone Formation

Journal

ADVANCED FUNCTIONAL MATERIALS
Volume 30, Issue 14, Pages -

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/adfm.201906205

Keywords

bone formation; cranio-maxillofacial surgery; multicomponent self-assembly; nanocomposite hydrogels; nanosilicates; self- assembling peptides

Funding

  1. ERC Starting Grant (STROFUNSCAFF)
  2. UK Regenerative Medicine Platform (UKRMP2) Acellular Smart Materials
  3. UK Regenerative Medicine Platform Hub Acellular SMART materials 3D architecture [MR/R015651/1]
  4. UK Regenerative Medicine Platform [MR/L012626/1]
  5. AO Foundation [AOCMF-17-19M]
  6. EPSRC [EP/L010259/1]
  7. National Key Research and Development Program of China [2016YFC1102800]
  8. National Natural Science Foundation of China [81870741]
  9. Technological Institute of the Philippines
  10. EPSRC [EP/L010259/1, EP/S017054/1] Funding Source: UKRI
  11. MRC [MR/R015651/1, MR/L012626/1] Funding Source: UKRI

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Synthetic osteo-promoting materials that are able to stimulate and accelerate bone formation without the addition of exogenous cells or growth factors represent a major opportunity for an aging world population. A co-assembling system that integrates hyaluronic acid tyramine (HA-Tyr), bioactive peptide amphiphiles (GHK-Cu2+), and Laponite (Lap) to engineer hydrogels with physical, mechanical, and biomolecular signals that can be tuned to enhance bone regeneration is reported. The central design element of the multicomponent hydrogels is the integration of self-assembly and enzyme-mediated oxidative coupling to optimize structure and mechanical properties in combination with the incorporation of an osteo- and angio-promoting segments to facilitate signaling. Spectroscopic techniques are used to confirm the interplay of orthogonal covalent and supramolecular interactions in multicomponent hydrogel formation. Furthermore, physico-mechanical characterizations reveal that the multicomponent hydrogels exhibit improved compressive strength, stress relaxation profile, low swelling ratio, and retarded enzymatic degradation compared to the single component hydrogels. Applicability is validated in vitro using human mesenchymal stem cells and human umbilical vein endothelial cells, and in vivo using a rabbit maxillary sinus floor reconstruction model. Animals treated with the HA-Tyr-HA-Tyr-GHK-Cu2+ hydrogels exhibit significantly enhanced bone formation relative to controls including the commercially available Bio-Oss.

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