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Characterisation of osteogenic and vascular responses of hMSCs to Ti-Co doped phosphate glass microspheres using a microfluidic perfusion platform.
Peticone, Carlotta; Thompson, David De Silva; Dimov, Nikolay; Jevans, Ben; Glass, Nick; Micheletti, Martina; Knowles, Jonathan C; Kim, Hae-Won; Cooper-White, Justin J; Wall, Ivan B.
Affiliation
  • Peticone C; Department of Biochemical Engineering, University College London, London, UK.
  • Thompson DS; Department of Biochemical Engineering, University College London, London, UK.
  • Dimov N; Centre for Engineering Research, University of Hertfordshire, Hatfield, Hertfordshire, UK.
  • Jevans B; Great Ormond Street Institute of Child Health, University College London, London, UK.
  • Glass N; Australian Institute for Bioengineering and Nanotechnology, University of Queensland, St. Lucia, Brisbane, Australia.
  • Micheletti M; Department of Biochemical Engineering, University College London, London, UK.
  • Knowles JC; Division of Biomaterials and Tissue Engineering, University College London Eastman Dental Institute, London, UK.
  • Kim HW; The Discoveries Centre for Regenerative and Precision Medicine, UCL Campus, London, UK.
  • Cooper-White JJ; Department of Nanobiomedical Science & BK21 PLUS NBM Global Research Center for Regenerative Medicine, Dankook University, Cheonan, Republic of Korea.
  • Wall IB; UCL Eastman-Korea Dental Medicine Innovation Centre, Dankook University, Cheonan, Republic of Korea.
J Tissue Eng ; 11: 2041731420954712, 2020.
Article in En | MEDLINE | ID: mdl-33178409
ABSTRACT
Using microspherical scaffolds as building blocks to repair bone defects of specific size and shape has been proposed as a tissue engineering strategy. Here, phosphate glass (PG) microcarriers doped with 5 mol % TiO2 and either 0 mol % CoO (CoO 0%) or 2 mol % CoO (CoO 2%) were investigated for their ability to support osteogenic and vascular responses of human mesenchymal stem cells (hMSCs). Together with standard culture techniques, cell-material interactions were studied using a novel perfusion microfluidic bioreactor that enabled cell culture on microspheres, along with automated processing and screening of culture variables. While titanium doping was found to support hMSCs expansion and differentiation, as well as endothelial cell-derived vessel formation, additional doping with cobalt did not improve the functionality of the microspheres. Furthermore, the microfluidic bioreactor enabled screening of culture parameters for cell culture on microspheres that could be potentially translated to a scaled-up system for tissue-engineered bone manufacturing.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: J Tissue Eng Year: 2020 Document type: Article Affiliation country: Reino Unido

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: J Tissue Eng Year: 2020 Document type: Article Affiliation country: Reino Unido
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