Nanoscale Structure–Activity Relationships, Mode of Action, and Biocompatibility of Gold Nanoparticle Antibiotics

The emergence of resistance to multiple antimicrobial agents by pathogenic bacteria has become a significant global public health threat. Multi-drug-resistant (MDR) Gram-negative bacteria have become particularly problematic, as no new classes of small-molecule antibiotics for Gram-negative bacteria...

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Veröffentlicht in:Journal of the American Chemical Society 2014-04, Vol.136 (14), p.5295-5300
Hauptverfasser: Bresee, Jamee, Bond, Constance M, Worthington, Roberta J, Smith, Candice A, Gifford, Jennifer C, Simpson, Carrie A, Carter, Carly J, Wang, Guankui, Hartman, Jesse, Osbaugh, Niki A, Shoemaker, Richard K, Melander, Christian, Feldheim, Daniel L
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container_end_page 5300
container_issue 14
container_start_page 5295
container_title Journal of the American Chemical Society
container_volume 136
creator Bresee, Jamee
Bond, Constance M
Worthington, Roberta J
Smith, Candice A
Gifford, Jennifer C
Simpson, Carrie A
Carter, Carly J
Wang, Guankui
Hartman, Jesse
Osbaugh, Niki A
Shoemaker, Richard K
Melander, Christian
Feldheim, Daniel L
description The emergence of resistance to multiple antimicrobial agents by pathogenic bacteria has become a significant global public health threat. Multi-drug-resistant (MDR) Gram-negative bacteria have become particularly problematic, as no new classes of small-molecule antibiotics for Gram-negative bacteria have emerged in over two decades. We have developed a combinatorial screening process for identifying mixed ligand monolayer/gold nanoparticle conjugates (2.4 nm diameter) with antibiotic activity. The method previously led to the discovery of several conjugates with potent activity against the Gram-negative bacterium Escherichia coli. Here we show that these conjugates are also active against MDR E. coli and MDR Klebsiella pneumoniae. Moreover, we have shown that resistance to these nanoparticles develops significantly more slowly than to a commercial small-molecule drug. These results, combined with their relatively low toxicity to mammalian cells and biocompatibility in vivo, suggest that gold nanoparticles may be viable new candidates for the treatment of MDR Gram-negative bacterial infections.
doi_str_mv 10.1021/ja408505n
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subjects Anti-Bacterial Agents - chemical synthesis
Anti-Bacterial Agents - chemistry
Anti-Bacterial Agents - pharmacology
Biocompatible Materials - chemical synthesis
Biocompatible Materials - chemistry
Biocompatible Materials - pharmacology
Dose-Response Relationship, Drug
Drug Resistance, Multiple, Bacterial - drug effects
Escherichia coli - drug effects
Gold - chemistry
Gold - pharmacology
Klebsiella pneumoniae - drug effects
Metal Nanoparticles - chemistry
Microbial Sensitivity Tests
Structure-Activity Relationship
title Nanoscale Structure–Activity Relationships, Mode of Action, and Biocompatibility of Gold Nanoparticle Antibiotics
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