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替加环素——一种新型甘氨酰环素类抗菌药物的药代动力学/药效学概况。

Pharmacokinetic/pharmacodynamic profile for tigecycline-a new glycylcycline antimicrobial agent.

作者信息

Meagher Alison K, Ambrose Paul G, Grasela Thaddeus H, Ellis-Grosse Evelyn J

机构信息

Department of Clinical Pharmacology, Cognigen Corporation, Buffalo, NY 14221, USA.

出版信息

Diagn Microbiol Infect Dis. 2005 Jul;52(3):165-71. doi: 10.1016/j.diagmicrobio.2005.05.006.

Abstract

Tigecycline is a new first-in-class glycylcycline antimicrobial agent with expanded broad-spectrum activity against both Gram-negative and Gram-positive aerobes and anaerobes, as well as atypical bacterial species. The spectrum of activity extends to clinically relevant susceptible and multidrug-resistant strains of Staphylococcus aureus, Streptococcus pneumoniae, vancomycin-resistant enterococci, and Enterobacteriaceae, including extended-spectrum beta-lactamase-producing strains. Tigecycline is administered as an intravenous formulation and has been studied in the treatment of serious polymicrobial infections, including complicated skin and skin-structure infections and intra-abdominal infections. Pharmacokinetic analysis of data from phase 1 trials of healthy subjects indicate that tigecycline has a large volume of distribution, signifying extensive tissue penetration, and a long terminal elimination half-life (approximately 40 h), easily allowing for twice-daily dose administration. Tigecycline penetrates well into blister fluid, which supports the positive findings of phase 2 and 3 studies of the efficacy of tigecycline in the treatment of serious skin and skin-structure infections. Metabolic studies in humans have revealed that tigecycline undergoes very limited metabolism and the primary route of elimination of unchanged drug is through the feces, with glucuronidation and renal elimination as secondary routes. A preliminary pharmacokinetic (PK)/pharmacodynamic analysis in experimental animal models of infection indicates that the efficacy of tigecycline is probably best predicted by the ratio of the area under the concentration-time curve to the minimum inhibitory concentration. The expanded in vitro activity against a broad range of bacteria, including resistant pathogens, and favorable PK profile of tigecycline suggest that this novel antimicrobial agent should offer clinicians an option for the treatment of patients with serious bacterial infections.

摘要

替加环素是一种新型的甘氨酰环素类抗菌药物,属于该类药物中的首个品种,对革兰氏阴性菌和革兰氏阳性需氧菌及厌氧菌以及非典型细菌均具有广泛的抗菌活性。其抗菌谱涵盖了临床上相关的金黄色葡萄球菌、肺炎链球菌、耐万古霉素肠球菌和肠杆菌科细菌的敏感及多重耐药菌株,包括产超广谱β-内酰胺酶的菌株。替加环素通过静脉制剂给药,已被用于治疗严重的多微生物感染,包括复杂皮肤及皮肤软组织感染和腹腔内感染。对健康受试者1期试验数据的药代动力学分析表明,替加环素分布容积大,意味着其组织穿透力强,且终末消除半衰期长(约40小时),便于每日给药两次。替加环素能很好地渗透到水疱液中,这支持了替加环素治疗严重皮肤及皮肤软组织感染的2期和3期研究的阳性结果。人体代谢研究显示,替加环素的代谢非常有限,药物原形的主要消除途径是通过粪便,次要途径是葡萄糖醛酸化和经肾消除。在感染实验动物模型中进行的初步药代动力学(PK)/药效学分析表明,替加环素的疗效可能最好通过浓度-时间曲线下面积与最低抑菌浓度之比来预测。替加环素对包括耐药病原体在内的多种细菌具有广泛的体外活性,且药代动力学特征良好,这表明这种新型抗菌药物应为临床医生治疗严重细菌感染患者提供一种选择。

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