Ball A P, Gray J A, Murdoch J M
Drugs. 1975;10(1):1-55. doi: 10.2165/00003495-197510010-00001.
Since the development of the sulphonamides in the 1930s and the subsequent development of antibiotics from the 1940s onwards, there have now been many drugs developed which are capable of chemotherapeutic activity in a patient infected by a susceptible micro-organism. This review is concerned with precise descriptions of important groups of antimicrobial drugs, with emphasis being placed on the more recently developed drugs. With each group of drugs the pharmacology, major therapeutic indications, dosages and adverse reactions are discussed. Part I of the article discusses the sulphonamides, the natural and semi-synthetic penicillins, cotrimoxazole, chloramphenicol, tetracyclines, the macrolides, lincomycin and clindamycin, fusidic acid, and the urinary antiseptics. The place of each in therapy is defined.
自20世纪30年代磺胺类药物问世以及随后从40年代起抗生素不断发展以来,现已研发出许多药物,这些药物能够对受易感微生物感染的患者发挥化疗活性。本综述关注抗菌药物重要类别的确切描述,重点放在近期研发的药物上。针对每类药物,都讨论了其药理学、主要治疗适应证、剂量及不良反应。本文第一部分讨论了磺胺类药物、天然和半合成青霉素、复方新诺明、氯霉素、四环素、大环内酯类、林可霉素和克林霉素、夫西地酸以及尿路抗菌药。明确了每种药物在治疗中的地位。