Agwuh Kenneth N, MacGowan Alasdair
Department of Medical Microbiology, Old Medical School, Leeds General Infirmary Great George Street, Leeds LS1 2EX, UK.
J Antimicrob Chemother. 2006 Aug;58(2):256-65. doi: 10.1093/jac/dkl224. Epub 2006 Jul 1.
The pharmacokinetics of tetracyclines and glycylcyclines are described in three groups. Group 1, the oldest group, represented by tetracycline, oxytetracycline, chlortetracycline, demeclocycline, lymecycline, methacycline and rolitetracycline is characterized by poor absorption after food. Group 2, represented by doxycycline and minocycline, is more reliably absorbed orally, while group 3, represented by the glycylcycline tigecycline, is injectable only, with an improved antibacterial spectrum compared with the tetracyclines. Though incompletely understood, the pharmacodynamic properties of the tetracyclines and glycylcyclines are summarized.
四环素类和甘氨酰环素类的药代动力学分为三组进行描述。第一组是最古老的一组,以四环素、土霉素、金霉素、地美环素、赖甲环素、美他环素和罗利环素为代表,其特点是进食后吸收较差。第二组以多西环素和米诺环素为代表,口服吸收更可靠,而第三组以甘氨酰环素替加环素为代表,仅可注射使用,与四环素类相比抗菌谱有所改善。尽管尚未完全了解,但对四环素类和甘氨酰环素类的药效学特性进行了总结。