Show simple item record

dc.contributor.authorGoreham, R.
dc.contributor.authorMierczynska, A.
dc.contributor.authorSmith, L.
dc.contributor.authorSedev, Rossen
dc.contributor.authorVasilev, K.
dc.date.accessioned2017-06-23T03:00:22Z
dc.date.available2017-06-23T03:00:22Z
dc.date.created2017-06-19T03:39:44Z
dc.date.issued2013
dc.identifier.citationGoreham, R. and Mierczynska, A. and Smith, L. and Sedev, R. and Vasilev, K. 2013. Small surface nanotopography encourages fibroblast and osteoblast cell adhesion. RSC Advances. 3 (26): pp. 10309-10317.
dc.identifier.urihttp://hdl.handle.net/20.500.11937/53569
dc.identifier.doi10.1039/c3ra23193c
dc.description.abstract

In this paper, we report the initial response of 3T3 fibroblast and MG63 osteoblast cells to engineered nanotopography gradients of three nanoparticle diameters (16 nm, 38 nm and 68 nm). These nanoengineered surfaces were designed to provide a range of nanoparticle densities and comparable surface area across the gradients of different nanoparticle sizes. Importantly, we provided a uniform surface chemistry in order to be able to examine the effect of pure surface nanotopography. We found that nanotopography features of 16 nm encourage the adhesion of both cell types and that there is a critical nanoparticle density between 50 and 140 particles per µm2 where cells adhered in the greatest numbers. When nanotopography features increased to 38 nm the 3T3 cells adhered and spread well, however, the MG63 cells adhered and spread poorly. Both cell types adhered in lower numbers when the nanotopography feature size increased to 68 nm. This work demonstrates that there is a specific nanotopography scale that encourages cell adhesion and spreading, however, the preferential lateral spacing and height of the nanotopography is different for different cell types.

dc.publisherRoyal Society of Chemistry
dc.titleSmall surface nanotopography encourages fibroblast and osteoblast cell adhesion
dc.typeJournal Article
dcterms.source.volume3
dcterms.source.number26
dcterms.source.startPage10309
dcterms.source.endPage10317
dcterms.source.issn2046-2069
dcterms.source.titleRSC Advances
curtin.departmentDepartment of Chemical Engineering
curtin.accessStatusFulltext not available


Files in this item

FilesSizeFormatView

There are no files associated with this item.

This item appears in the following Collection(s)

Show simple item record