Gootz T D
Pfizer Central Research, Groton, Connecticut 06340.
Clin Microbiol Rev. 1990 Jan;3(1):13-31. doi: 10.1128/CMR.3.1.13.
The unprecedented growth in the number of new antibiotics over the past two decades has been the result of extensive research efforts that have exploited the growing body of knowledge describing the interactions of antibiotics with their targets in bacterial cells. Information gained from one class of antimicrobial agents has often been used to advance the development of other classes. In the case of beta-lactams, information on structure-activity relationships gleaned from penicillins and cephalosporins was rapidly applied to the cephamycins, monobactams, penems, and carbapenems in order to discover broad-spectrum agents with markedly improved potency. These efforts have led to the introduction of many new antibiotics that demonstrate outstanding clinical efficacy and improved pharmacokinetics in humans. The current review discusses those factors that have influenced the rapid proliferation of new antimicrobial agents, including the discovery of new lead structures from natural products and the impact of bacterial resistance development in the clinical setting. The development process for a new antibiotic is discussed in detail, from the stage of early safety testing in animals through phase I, II, and III clinical trials.
在过去二十年中,新型抗生素数量的空前增长是广泛研究努力的结果,这些努力利用了越来越多关于抗生素与其在细菌细胞中的靶点相互作用的知识。从一类抗菌剂中获得的信息常常被用于推动其他类抗菌剂的开发。就β-内酰胺类抗生素而言,从青霉素和头孢菌素中收集到的构效关系信息迅速应用于头霉素类、单环β-内酰胺类、青霉烯类和碳青霉烯类抗生素,以发现效力显著提高的广谱药物。这些努力已带来许多新型抗生素的问世,这些抗生素在人体中显示出卓越的临床疗效和改善的药代动力学特性。本综述讨论了影响新型抗菌剂迅速增多的因素,包括从天然产物中发现新的先导结构以及临床环境中细菌耐药性发展的影响。详细讨论了新型抗生素的研发过程,从动物早期安全性测试阶段到I、II和III期临床试验阶段。