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Gold nanoparticle interactions with endothelial cells cultured under physiological conditions
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Freese, C., Anspach, L., Deller, Robert C., Richards, Sarah-Jane, Gibson, Matthew I., Kirkpatrick, C. J. and Unger, R. E. (2017) Gold nanoparticle interactions with endothelial cells cultured under physiological conditions. Biomaterials Science, 5 (4). pp. 707-717. doi:10.1039/C6BM00853D ISSN 2047-4830.
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Official URL: http://dx.doi.org/10.1039/C6BM00853D
Abstract
PEGylated gold nanoparticles (AuNPs) have an extended circulation time after intravenous injection in vivo and exhibit favorable properties for biosensing, diagnostic imaging, and cancer treatment. No impact of PEGylated AuNPs on the barrier forming properties of endothelial cells (ECs) has been reported, but recent studies demonstrated that unexpected effects on erythrocytes are observed. Almost all studies to date have been with static-cultured ECs. Herein, ECs maintained under physiological cyclic stretch and flow conditions and used to generate a blood–brain barrier model were exposed to 20 nm PEGylated AuNPs. An evaluation of toxic effects, cell stress, the release profile of pro-inflammatory cytokines, and blood–brain barrier properties showed that even under physiological conditions no obvious effects of PEGylated AuNPs on ECs were observed. These findings suggest that 20 nm-sized, PEGylated AuNPs may be a useful tool for biomedical applications, as they do not affect the normal function of healthy ECs after entering the blood stream.
| Item Type: | Journal Article | ||||||||||
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| Subjects: | Q Science > QP Physiology R Medicine > R Medicine (General) |
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| Divisions: | Faculty of Science, Engineering and Medicine > Science > Chemistry | ||||||||||
| Library of Congress Subject Headings (LCSH): | Nanoparticles, Endothelial cells, Gold, Biomedical materials, Metals in medicine, Erythrocytes | ||||||||||
| Journal or Publication Title: | Biomaterials Science | ||||||||||
| Publisher: | R S C Publications | ||||||||||
| ISSN: | 2047-4830 | ||||||||||
| Official Date: | 1 April 2017 | ||||||||||
| Dates: |
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| Volume: | 5 | ||||||||||
| Number: | 4 | ||||||||||
| Page Range: | pp. 707-717 | ||||||||||
| DOI: | 10.1039/C6BM00853D | ||||||||||
| Status: | Peer Reviewed | ||||||||||
| Publication Status: | Published | ||||||||||
| Access rights to Published version: | Restricted or Subscription Access | ||||||||||
| Date of first compliant deposit: | 14 February 2017 | ||||||||||
| Date of first compliant Open Access: | 10 February 2018 | ||||||||||
| Funder: | Advantage West Midlands (AWM), European Regional Development Fund (ERDF), Engineering and Physical Sciences Research Council (EPSRC), University of Warwick. Molecular Organisation and Assembly in Cells (MOAC), Seventh Framework Programme (European Commission) (FP7) | ||||||||||
| Grant number: | NMP4-CT-2006-026723 (FP7) |
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