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    Biological response of human suture mesenchymal cells to Titania nanotube-based implants for advanced craniosynostosis therapy

    Year: 2017

    Journal: Colloid Surf. B-Biointerfaces, Volume 150, FEB 1, page 59–67

    Authors: Banana, Manpreet; Dwivedi, Prern; Ranjitkar, Sarbin; Kaidonis, John A.; Losic, Dusan; Anderson, Peter J.

    Organizations: Australian Dental Research Foundation [ADRF-18/2013]; Australian Research Council [ARC -FT110100711]; Australian Craniomaxillofacial Foundation

    Keywords: Craniosynostosis; Protein-releasing implants; Titania nanotubes; Cranial implants; Human suture mesenchymal cells; Cellular response

    Titania nanotubes (TNTs) engineered on titanium (Ti) surfaces (i.e. TNT/Ti) and loaded with specific drugs have been recognised as a promising solution for localised therapeutic delivery to address several medical problems not feasible with conventional drug administration. We propose the use of TNT/Ti protein-releasing implants to treat paediatric craniofacial abnormality in craniosynostosis caused by premature fusion of cranial sutures. In this study, we have analysed the biological response of human suture mesenchymal cells (SMCs), extracted from two different patients undergoing craniofacial reconstruction surgery, at the TNT/Ti implant surface. The experimental groups included large-diameter TNT/Ti implants, with and without biopolymer surface coating (Chitosan and Pluronic-F127) while the controls comprised of flat Ti disc and tissue culture plastic. The non-loaded implant surfaces and the cellular interactions at the implant-cell interface were characterised using scanning electron microscopy (SEM). The SMC adhesion, viability and proliferation were determined by MTT assay and manual cell counting at day 1 and day 3 of cell incubation. SEM showed significant reduction in initial attachment and adhesion of SMCs at TNT-cell biointerface compared with the control Ti discs. Subsequent cell proliferation results also revealed a decrease in the number of viable cells on the TNT surfaces. The nanotopography and structural features along with the surface chemistry dictated the cellular response, with nanotubular surfaces (with and without polymer coating) impeding cell adhesion and proliferation. Our findings hold promise for the use of TNT-based cranial implants as a delivery system to prevent sutural bone growth for advanced craniosynostosis therapy. (C) 2016 Elsevier B.V. All rights reserved.
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