Polymyxin B versus colistin: an update

被引:107
作者
Cai, Yiying [1 ,3 ]
Lee, Winnie [1 ]
Kwa, Andrea L. [1 ,2 ,3 ]
机构
[1] Singapore Gen Hosp, Dept Pharm, Singapore 169608, Singapore
[2] Duke NUS Grad Med Sch, Emerging Infect Dis, Singapore 169857, Singapore
[3] Natl Univ Singapore, Dept Pharm, Singapore 119077, Singapore
关键词
colistimethate sodium; colistin sulfate; multi-drug resistance; pharmacokinetics and pharmacodynamics; polymyxin B; polymyxin combination therapy; polymyxins; polypeptide antibiotics; CRITICALLY-ILL PATIENTS; RESISTANT ACINETOBACTER-BAUMANNII; IN-VITRO PHARMACODYNAMICS; SODIUM SULPHOMETHYL DERIVATIVES; GRAM-NEGATIVE BACTERIA; MULTIDRUG-RESISTANT; PSEUDOMONAS-AERUGINOSA; COMBINATION THERAPY; POPULATION PHARMACOKINETICS; INDUCED NEPHROTOXICITY;
D O I
10.1586/14787210.2015.1093933
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Polymyxin B and colistin (polymyxin E) are polypeptide antibiotics that were developed in the 1940s, but fell into disfavor due to their high toxicity rates. These two antibiotics were previously regarded to be largely equivalent, due to similarities in their chemical structure and spectrum of activity. In recent years, several pertinent differences, especially in terms of potency and disposition, have been revealed between polymyxin B and colistin. These differences are mainly attributed to the fact that polymyxin B is administered parenterally in its active form, while colistin is administered parenterally as an inactive pro-drug, colistimethate. In this review, we summarize the similarities and differences between polymyxin B and colistin. We also discuss the potential clinical implications of these findings, and provide our perspectives on how polymyxins should be employed to preserve their utility in this era of multi-drug resistance.
引用
收藏
页码:1481 / 1497
页数:17
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