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Targeted Delivery of Glucan Particle Encapsulated Gallium Nanoparticles Inhibits HIV Growth in Human Macrophages

Soto, Ernesto R
O'Connell, Olivia
Dikengil, Fusun
Peters, Paul J.
Clapham, Paul R.
Ostroff, Gary R
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Faculty Advisor
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UMass Chan Affiliations
Document Type
Journal Article
Publication Date
2016-12-14
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Abstract

Glucan particles (GPs) are hollow, porous 3-5 mum microspheres derived from the cell walls of Baker's yeast (Saccharomyces cerevisiae). The 1,3-beta-glucan outer shell provides for receptor-mediated uptake by phagocytic cells expressing beta-glucan receptors. GPs have been used for macrophage-targeted delivery of a wide range of payloads (DNA, siRNA, protein, small molecules, and nanoparticles) encapsulated inside the hollow GPs or bound to the surface of chemically derivatized GPs. Gallium nanoparticles have been proposed as an inhibitory agent against HIV infection. Here, macrophage targeting of gallium using GPs provides for more efficient delivery of gallium and inhibition of HIV infection in macrophages compared to free gallium nanoparticles.

Source

J Drug Deliv. 2016;2016:8520629. Epub 2016 Nov 14. Link to article on publisher's site

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DOI
10.1155/2016/8520629
PubMed ID
27965897
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Copyright © 2016 Ernesto R. Soto et al.