Antimicrobial resistance challenged with metal-based antimicrobial macromolecules

被引:81
作者
Abd-El-Aziz, Alaa S. [1 ]
Agatemor, Christian [1 ]
Etkin, Nola [1 ]
机构
[1] Univ Prince Edward Isl, Dept Chem, Charlottetown, PE C1A 4P3, Canada
关键词
Antimicrobial resistance; Metal-based antimicrobial macromolecules; Metal-based antimicrobial polymers; Organometallic antimicrobial compounds; Contact-killing materials; BIOLOGICALLY-ACTIVE POLYMERS; REACTIVE OXYGEN; ANTIBACTERIAL ACTIVITY; COORDINATION POLYMERS; ORGANOMETALLIC COMPOUNDS; STAPHYLOCOCCUS-AUREUS; OXIDATIVE STRESS; KILL BACTERIA; ORGANOTIN; ANTIBIOTICS;
D O I
10.1016/j.biomaterials.2016.12.002
中图分类号
R318 [生物医学工程];
学科分类号
100103 [病原生物学];
摘要
Antimicrobial resistance threatens the achievements of science and medicine, as it deactivates conventional antimicrobial therapeutics. Scientists respond to the threat by developing new antimicrobial platforms to prevent and treat infections from these resistant strains. Metal-based antimicrobial macromolecules are emerging as an alternative to conventional platforms because they combine multiple mechanisms of action into one platform due to the distinctive properties of metals. For example, metals interact with intracellular proteins and enzymes, and catalyse various intracellular processes. The macromolecular architecture offers a means to enhance antimicrobial activity since several antimicrobial moieties can be conjugated to the scaffold. Further, these macromolecules can be fabricated into antimicrobial materials for contact-killing medical implants, fabrics, and devices. As volatilization or leaching out of the antimicrobial moieties from the macromolecular scaffold is reduced, these medical implants, fabrics, and devices can retain their antimicrobial activity over an extended period. Recent advances demonstrate the potential of metal-based antimicrobial macromolecules as effective platforms that prevent and treat infections from resistant strains. In this review these advances are thoroughly discussed within the context of examples of metal-based antimicrobial macromolecules, their mechanisms of action and biocompatibility. (C) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码:27 / 50
页数:24
相关论文
共 110 条
[1]
Abd-El-Aziz A.S., 2016, EUR POLYM J
[2]
Design of Piperazine Organoiron Macromolecules with Antibacterial and Anticancer Activity [J].
Abd-El-Aziz, Alaa S. ;
Abdelghani, Amani A. ;
Pearson, Jason K. ;
Awad, Mohamed K. ;
Overy, David P. ;
Kerr, Russell G. .
MACROMOLECULAR CHEMISTRY AND PHYSICS, 2016, 217 (08) :987-996
[3]
Antimicrobial Organometallic Dendrimers with Tunable Activity against Multidrug-Resistant Bacteria [J].
Abd-El-Aziz, Alaa S. ;
Agatemor, Christian ;
Etkin, Nola ;
Overy, David P. ;
Lanteigne, Martin ;
McQuillan, Katherine ;
Kerr, Russell G. .
BIOMACROMOLECULES, 2015, 16 (11) :3694-3703
[4]
Redox-active cationic organoiron complex: a promising lead structure for developing antimicrobial agents with activity against Gram-positive pathogens including methicillin-resistant Staphylococcus aureus and vancomycin-resistant Enterococcus faecium [J].
Abd-El-Aziz, Alaa S. ;
Agatemor, Christian ;
Etkin, Nola ;
Overy, David P. ;
Kerr, Russell G. .
RSC ADVANCES, 2015, 5 (105) :86421-86427
[5]
Abraham EP, 1941, LANCET, V2, P177
[6]
Highly active antibacterial ferrocenoylated or ruthenocenoylated Arg-Trp peptides can be discovered by an L-to-D substitution scan [J].
Albada, H. Bauke ;
Prochnow, Pascal ;
Bobersky, Sandra ;
Bandow, Julia E. ;
Metzler-Nolte, Nils .
CHEMICAL SCIENCE, 2014, 5 (11) :4453-4459
[7]
Modulating the activity of short arginine-tryptophan containing antibacterial peptides with N-terminal metallocenoyl groups [J].
Albada, H. Bauke ;
Chiriac, Alina-Iulia ;
Wenzel, Michaela ;
Penkova, Maya ;
Bandow, Julia E. ;
Sahl, Hans-Georg ;
Metzler-Nolte, Nils .
BEILSTEIN JOURNAL OF ORGANIC CHEMISTRY, 2012, 8 :1753-1764
[8]
Medical progress: Disorders of iron metabolism [J].
Andrews, NC .
NEW ENGLAND JOURNAL OF MEDICINE, 1999, 341 (26) :1986-1995
[9]
Trends in infectious disease mortality in the United States during the 20th century [J].
Armstrong, GL ;
Conn, LA ;
Pinner, RW .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1999, 281 (01) :61-66
[10]
AVRAMEAS S, 1967, J BIOL CHEM, V242, P1651