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Matthew S. P. Boyles

Researcher at University of Salzburg

Publications -  30
Citations -  1143

Matthew S. P. Boyles is an academic researcher from University of Salzburg. The author has contributed to research in topics: Medicine & Chemistry. The author has an hindex of 13, co-authored 22 publications receiving 914 citations. Previous affiliations of Matthew S. P. Boyles include Heriot-Watt University & Edinburgh Napier University.

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The oxidative potential of differently charged silver and gold nanoparticles on three human lung epithelial cell types

TL;DR: Chitosan functionalization of NPs, with resultant high surface charges plays an important role in NP-toxic effects and is dependent on the core material of the particle, the cell type used for testing and the growth characteristics of these cell culture model systems.
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Multi-walled carbon nanotube induced frustrated phagocytosis, cytotoxicity and pro-inflammatory conditions in macrophages are length dependent and greater than that of asbestos.

TL;DR: This study demonstrates that CNTs are potentially pathogenic, as they were routinely found to induce detrimental responses in macrophages greater than those induced by asbestos at the same mass-based dose.
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Is the toxic potential of nanosilver dependent on its size

TL;DR: Strong cytotoxic and genotoxic effects were observed in cells exposed to Ag ENMs 50 nm, but Ag ENM 200 nm had the most mutagenic potential, and it was found that the toxicity of Ag ENm is not always size dependent.
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Chitosan functionalisation of gold nanoparticles encourages particle uptake and induces cytotoxicity and pro-inflammatory conditions in phagocytic cells, as well as enhancing particle interactions with serum components.

TL;DR: It can be concluded that functionalisation of AuNPs with the perceived non-toxic biocompatible molecule chitosan at a high density can elicit functionalisation-dependent intracellular trafficking mechanisms and provoke strong pro-inflammatory conditions, and that a high affinity of these NP-conjugates for biomolecules may be implicit in these cellular responses.
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An investigation into the potential for different surface-coated quantum dots to cause oxidative stress and affect macrophage cell signalling in vitro.

TL;DR: Investigation of the ability of a series of different surface-coated quantum dots (QDs) to cause oxidative stress and affect cell signalling in J774.A1 macrophages concluded that QDs differ in their interactions with macrophage according to their specific surface properties.