Abstract
Core-shell nanostructures with nonionic amphiphilic shells and ionic cores encapsulating gentamicin were designed for therapy against intracellular pathogens, including Salmonella and Listeria. Flow cytometry and confocal microscopy showed that their uptake into J774A.1 macrophages proceeded mainly by fluid-phase endocytosis and clathrin-mediated pathways. The nanostructures were nontoxic in vitro at doses of 50 to 250 microg/ml, and they significantly reduced the amounts of intracellular Salmonella (0.53 log) and Listeria (3.16 log), thereby suggesting effective transport into the cells.
Publication types
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Research Support, Non-U.S. Gov't
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Research Support, U.S. Gov't, Non-P.H.S.
MeSH terms
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Anti-Bacterial Agents / chemistry
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Anti-Bacterial Agents / pharmacology
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Anti-Bacterial Agents / therapeutic use*
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Cell Line
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Drug Carriers / chemistry
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Drug Carriers / therapeutic use
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Flow Cytometry
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Gentamicins / chemistry
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Gentamicins / pharmacology
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Gentamicins / therapeutic use*
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Humans
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Listeria monocytogenes / drug effects
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Listeriosis / drug therapy*
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Listeriosis / microbiology
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Macrophages / microbiology
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Macrophages / ultrastructure
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Microscopy, Confocal
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Nanostructures / chemistry
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Nanostructures / therapeutic use*
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Salmonella Infections / drug therapy*
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Salmonella Infections / microbiology
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Salmonella typhimurium / drug effects
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Treatment Outcome
Substances
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Anti-Bacterial Agents
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Drug Carriers
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Gentamicins