New approaches in peptide antibiotics

被引:118
作者
Vaara, Martti [1 ,2 ]
机构
[1] No Antibiot Ltd, FI-00720 Helsinki, Finland
[2] Helsinki Univ Hosp, Div Clin Microbiol, FI-00029 Helsinki, Finland
关键词
ANTIMICROBIAL ACTIVITY; OMIGANAN PENTAHYDROCHLORIDE; ANTIBACTERIAL PEPTIDES; PSEUDOMONAS-AERUGINOSA; CATHELICIDIN LL-37; CATIONIC PEPTIDE; RESISTANCE; DEFENSINS; DESIGN; DERIVATIVES;
D O I
10.1016/j.coph.2009.08.002
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The emergence and rapid spread of extremely multiresistant bacteria necessitates every effort to develop novel antibacterial agents. Host-derived antimicrobial peptides (AMPs) pexiganan (a magainin), omiganan (an indolicidin), and iseganan (a protegrin) have been in clinical phases for more than 10 years and provide little in combating against those bacteria. Even though some recent approaches may yield more effective and better-tolerated derivatives of host-derived AMPs, most novel derivatives suffer from weak activity, nonspecific cytotoxicity, and apparent susceptibility to proteolysis. Few have undergone any systematic toxicity and efficacy studies. Bacterial peptides and their derivatives, such as lantibiotics, the RTA-3 peptide, and novel polymyxins, as well as certain peptidomimetics, such as ceragenins, might be more useful.
引用
收藏
页码:571 / 576
页数:6
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