Drug Delivery, Disposition and Dynamics, Monash Institute of Pharmaceutical Sciences, Melbourne, Australia.
Curr Opin Infect Dis. 2012 Dec;25(6):626-33. doi: 10.1097/QCO.0b013e328358afe5.
Increased emergence of bacterial resistance and the decline in newly developed antibiotics have necessitated the reintroduction of previously abandoned antimicrobial agents active against multidrug-resistant bacteria. Having never been subjected to contemporary drug development procedures, these 'old' antibiotics require redevelopment in order to optimize therapy. This review focuses on colistin as an exemplar of a successful redevelopment process and briefly discusses two other old antibiotics, fusidic acid and fosfomycin.
Redevelopment of colistin led to an improved understanding of its chemistry, pharmacokinetics and pharmacodynamics, enabling important steps towards optimizing its clinical use in different patient populations. A scientifically based dosing algorithm was developed for critically ill patients, including those with renal impairment. As nephrotoxicity is a dose-limiting adverse event of colistin, rational combination therapy with other antibiotics needs to be investigated.
The example of colistin demonstrated that state-of-the-art analytical, microbiological and pharmacokinetic/pharmacodynamic methods can facilitate optimized use of 'old' antibiotics in the clinic. Similar methods are now being applied to fosfomycin and fusidic acid in order to optimize therapy. To improve and preserve the usefulness of these antibiotics rational approaches for redevelopment need to be followed.
细菌耐药性的不断增加和新开发抗生素的减少,使得人们有必要重新引入先前被放弃的针对多药耐药菌的抗菌药物。这些“老”抗生素从未经过当代药物开发程序的检验,因此需要重新开发以优化治疗。本文以黏菌素为例,探讨了成功的重新开发过程,并简要讨论了另外两种老抗生素,即夫西地酸和磷霉素。
黏菌素的重新开发使人们对其化学、药代动力学和药效学有了更深入的了解,为优化其在不同患者群体中的临床应用迈出了重要的一步。为包括肾功能损害在内的危重症患者开发了一种基于科学的剂量算法。由于黏菌素的肾毒性是其剂量限制不良事件,因此需要研究与其他抗生素的合理联合治疗。
黏菌素的例子表明,最先进的分析、微生物学和药代动力学/药效学方法可以促进“老”抗生素在临床中的优化使用。目前正在应用类似的方法来优化磷霉素和夫西地酸的治疗。为了提高和保护这些抗生素的有效性,需要遵循合理的重新开发方法。