Tuning stable noble metal nanoparticles dispersions to moderate their interaction with model membranes.

Ag coated Au nanoparticles Ag nanoparticle dispersions Au nanoparticle dispersions Electrochemical membrane sensor Nanoparticle screening Vesicle leakage assay

Journal

Journal of colloid and interface science
ISSN: 1095-7103
Titre abrégé: J Colloid Interface Sci
Pays: United States
ID NLM: 0043125

Informations de publication

Date de publication:
15 Jul 2021
Historique:
received: 11 12 2020
revised: 26 02 2021
accepted: 01 03 2021
pubmed: 24 3 2021
medline: 22 6 2021
entrez: 23 3 2021
Statut: ppublish

Résumé

The properties of stable gold (Au) nanoparticle dispersions can be tuned to alter their activity towards biomembrane models. Au nanoparticle coating techniques together with rapid electrochemical screens of a phospholipid layer on fabricated mercury (Hg) on platinum (Pt) electrode have been used to moderate the phospholipid layer activity of Au nanoparticle dispersions. Screening results for Au nanoparticle dispersions were intercalibrated with phospholipid large unilamellar vesicle (LUV) interactions using a carboxyfluorescein (CF) leakage assay. All nanoparticle dispersions were characterised for size, by dynamic light scattering (DLS) and transmission electron microscopy (TEM). Commercial and high quality home synthesised Au nanoparticle dispersions are phospholipid monolayer active whereas Ag nanoparticle dispersions are not. If Au nanoparticles are coated with a thin layer of Ag then the particle/lipid interaction is suppressed. The electrochemical assays of the lipid layer activity of Au nanoparticle dispersions align with LUV leakage assays of the same. Au nanoparticles of decreasing size and increasing dispersion concentration showed a stronger phospholipid monolayer/bilayer interaction. Treating Au nanoparticles with cell culture medium and incubation of Au nanoparticle dispersions in phosphate buffered saline (PBS) solutions removes their phospholipid layer interaction.

Identifiants

pubmed: 33756358
pii: S0021-9797(21)00296-4
doi: 10.1016/j.jcis.2021.03.009
pii:
doi:

Substances chimiques

Phospholipids 0
Silver 3M4G523W1G
Gold 7440-57-5

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

101-112

Informations de copyright

Copyright © 2021 Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Nicola William (N)

School of Chemistry, University of Leeds, Leeds LS2 9JT, UK.

Faith Bamidoro (F)

School of Chemical and Process Engineering, University of Leeds, Leeds LS2 9JT, UK.

Paul A Beales (PA)

School of Chemistry, University of Leeds, Leeds LS2 9JT, UK; Bragg Centre for Materials Research, University of Leeds, Leeds LS2 9JT, UK; Astbury Centre for Structural Molecular Biology, University of Leeds, Leeds LS2 9JT, UK.

Rik Drummond-Brydson (R)

School of Chemical and Process Engineering, University of Leeds, Leeds LS2 9JT, UK; Bragg Centre for Materials Research, University of Leeds, Leeds LS2 9JT, UK.

Nicole Hondow (N)

School of Chemical and Process Engineering, University of Leeds, Leeds LS2 9JT, UK; Bragg Centre for Materials Research, University of Leeds, Leeds LS2 9JT, UK.

Sarah Key (S)

School of Chemistry, University of Leeds, Leeds LS2 9JT, UK.

Alexander Kulak (A)

School of Chemistry, University of Leeds, Leeds LS2 9JT, UK.

Aidan Charles Walsh (AC)

School of Chemistry, University of Leeds, Leeds LS2 9JT, UK.

Sophia Winter (S)

School of Chemistry, University of Leeds, Leeds LS2 9JT, UK.

Laurence Andrew Nelson (LA)

School of Chemistry, University of Leeds, Leeds LS2 9JT, UK. Electronic address: a.l.nelson@leeds.ac.uk.

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Classifications MeSH