Lacey R W, Lord V L, Howson G L
J Antimicrob Chemother. 1984 Jan;13(1):5-13. doi: 10.1093/jac/13.1.5.
Miokamycin is a diacetyl derivative of the macrolide antibiotic, midecamycin. In vitro, it has an unusual spectrum, inhibiting the growth of Gram-positive cocci and anaerobes, but few Haemophilus spp; enterobacteria are highly resistant. Most erythromycin-resistant Staphylococcus aureus were sensitive (MIC approximately 0.8 mg/l). Resistance to miokamycin in Staph. aureus and streptococci was difficult to select, unless the staphylococci were already resistant to erythromycin. Both miokamycin and erythromycin were bactericidal towards groups A,B,C and G streptococci. Clinical trials of the drug in pelvic, upper respiratory, skin and soft tissue and other staphylococcal infections may be worthwhile.
米欧卡霉素是大环内酯类抗生素麦迪霉素的二乙酰衍生物。在体外,它具有不寻常的抗菌谱,能抑制革兰氏阳性球菌和厌氧菌的生长,但对嗜血杆菌属作用甚微;肠杆菌对其高度耐药。大多数对红霉素耐药的金黄色葡萄球菌对米欧卡霉素敏感(最低抑菌浓度约为0.8毫克/升)。在金黄色葡萄球菌和链球菌中很难筛选出对米欧卡霉素的耐药菌,除非这些葡萄球菌已对红霉素耐药。米欧卡霉素和红霉素对A、B、C和G组链球菌均有杀菌作用。该药物在盆腔、上呼吸道、皮肤和软组织以及其他葡萄球菌感染方面的临床试验可能是值得的。