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dc.contributor.authorShafaie, Sara
dc.contributor.authorHutter, Victoria
dc.contributor.authorBrown, Marc
dc.contributor.authorCook, Michael
dc.contributor.authorChau, David
dc.date.accessioned2017-11-15T18:15:32Z
dc.date.available2017-11-15T18:15:32Z
dc.date.issued2017-10-30
dc.identifier.citationShafaie , S , Hutter , V , Brown , M , Cook , M & Chau , D 2017 , ' Influence of surface geometry on the culture of human cell lines: a comparative study using flat, round-bottom and v-shaped 96 well plates ' , PLoS ONE , vol. 12 , no. 10 , e0186799 . https://doi.org/10.1371/journal.pone.0186799
dc.identifier.issn1932-6203
dc.identifier.urihttp://hdl.handle.net/2299/19524
dc.description© 2017 Shafaie et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
dc.description.abstractIn vitro cell based models have been invaluable tools for studying cell behaviour and for investigating drug disposition, toxicity and potential adverse effects of administered drugs. Within this drug discovery pipeline, the ability to assess and prioritise candidate compounds as soon as possible offers a distinct advantage. However, the ability to apply this approach to a cell culture study is limited by the need to provide an accurate, in vitro-like, microenvironment in conjunction with a low cost and high-throughput screening (HTS) methodology. Although the geometry and/or alignment of cells has been reported to have a profound influence on cell growth and differentiation, only a handful of studies have directly compared the growth of a single cell line on different shaped multiwell plates the most commonly used substrate for HTS, in vitro, studies. Herein, the impact of various surface geometries (flat, round and v-shaped 96 well plates), as well as fixed volume growth media and fixed growth surface area have been investigated on the characteristics of three commonly used human cell lines in biopharmaceutical research and development, namely ARPE-19 (retinal epithelial), A549 (alveolar epithelial) and Malme-3M (dermal fibroblastic) cells. The effect of the surface curvature on cells was characterised using a combination of a metabolic activity assay (CellTiter AQ/MTS), LDH release profiles (CytoTox ONE) and absolute cell counts (Guava ViaCount), respectively. In addition, cell differentiation and expression of specific marker proteins were determined using flow cytometry. These in vitro results confirmed that surface topography had a significant effect (p < 0.05) on cell activity and morphology. However, although specific marker proteins were expressed on day 1 and 5 of the experiment, no significant differences were seen between the different plate geometries (p < 0.05) at the later time point. Accordingly, these results highlight the impact of substrate geometry on the culture of a cell line and the influence it has on the cells' correct growth and differentiation characteristics. As such, these results provide important implications in many aspects of cell biology the development of a HTS, in vitro, cell based systems to further investigate different aspects of toxicity testing and drug delivery.en
dc.format.extent5355853
dc.language.isoeng
dc.relation.ispartofPLoS ONE
dc.titleInfluence of surface geometry on the culture of human cell lines: a comparative study using flat, round-bottom and v-shaped 96 well platesen
dc.contributor.institutionSchool of Life and Medical Sciences
dc.contributor.institutionDepartment of Pharmacy, Pharmacology and Postgraduate Medicine
dc.contributor.institutionCentre for Research into Topical Drug Delivery and Toxicology
dc.contributor.institutionAirway Group
dc.contributor.institutionPharmaceutics
dc.contributor.institutionSkin and Nail Group
dc.contributor.institutionBioadhesive Drug Delivery Group
dc.contributor.institutionNanopharmaceutics
dc.contributor.institutionPharmaceutical Analysis and Product Characterisation
dc.contributor.institutionToxicology
dc.description.statusPeer reviewed
dc.identifier.urlhttps://www.ncbi.nlm.nih.gov/pubmed/29084285
rioxxterms.versionofrecord10.1371/journal.pone.0186799
rioxxterms.typeJournal Article/Review
herts.preservation.rarelyaccessedtrue


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