Cubist Pharmaceuticals, Inc., 65 Hayden Avenue, Lexington, MA 02421, USA.
J Antimicrob Chemother. 2012 Oct;67(10):2463-9. doi: 10.1093/jac/dks246. Epub 2012 Jul 6.
Appropriate antibiotic exposure at the site of infection is important for clinically effective therapy. This study compared the epithelial lining fluid (ELF) penetration of ceftolozane/tazobactam, which has potent in vitro activity against many Gram-negative pathogens causing nosocomial pneumonia, with that of piperacillin/tazobactam in healthy adult volunteers.
In this Phase 1, open-label trial, 51 healthy adult subjects were randomized to receive three doses of either ceftolozane/tazobactam 1.5 g administered every 8 h via a 60 min infusion or piperacillin/tazobactam 4.5 g administered every 6 h via a 30 min infusion. Serial blood samples were obtained for determination of plasma drug concentrations. Bronchoscopy and bronchoalveolar lavage were performed at pre-specified timepoints in five subjects per timepoint in each treatment group to determine the ELF drug concentration. The penetration of individual analytes into the ELF was determined from the ratio of the area under the plasma concentration-time curve in ELF to that in plasma (AUC(ELF)/AUC(plasma)).
Plasma and ELF concentrations of ceftolozane, piperacillin and tazobactam increased rapidly, reaching maximal concentrations at the end of the infusion. Mean maximum concentration and AUC from time 0 to the end of the dosing interval (AUC(0-τ)) for ceftolozane in ELF were 21.8 mg/L and 75.1 mg·h/L, respectively. Corresponding values for piperacillin were 58.8 mg/L and 94.5 mg·h/L. The ELF/plasma AUC ratio for ceftolozane was 0.48 compared with 0.26 for piperacillin.
This study demonstrated that ceftolozane penetrated well into the ELF following parenteral administration of ceftolozane/tazobactam.
感染部位适当的抗生素暴露对于临床有效治疗很重要。本研究比较了头孢洛扎/他唑巴坦(ceftolozane/tazobactam)的上皮衬液(ELF)穿透率,该药物对引起医院获得性肺炎的许多革兰氏阴性病原体具有强大的体外活性,与健康成年志愿者中哌拉西林/他唑巴坦的穿透率进行比较。
在这项 1 期、开放标签试验中,51 名健康成年受试者随机分为两组,分别接受 3 次剂量的头孢洛扎/他唑巴坦 1.5 g,每 8 小时给药 1 次,输注时间为 60 分钟;或哌拉西林/他唑巴坦 4.5 g,每 6 小时给药 1 次,输注时间为 30 分钟。在每个治疗组的每个时间点,每个时间点均有 5 名受试者进行连续采血以测定血浆药物浓度。支气管镜检查和支气管肺泡灌洗在每个治疗组的每个时间点的 5 名受试者中进行,以确定 ELF 药物浓度。通过 ELF 中的药物浓度与血浆中的药物浓度(AUC(ELF)/AUC(血浆))的比值确定单个分析物进入 ELF 的穿透率。
头孢洛扎、哌拉西林和他唑巴坦的血浆和 ELF 浓度迅速增加,在输注结束时达到最大浓度。头孢洛扎在 ELF 中的平均最大浓度和 AUC 从 0 时间到给药间隔结束时间(AUC(0-τ))分别为 21.8 mg/L 和 75.1 mg·h/L,相应的哌拉西林浓度分别为 58.8 mg/L 和 94.5 mg·h/L。头孢洛扎的 ELF/血浆 AUC 比值为 0.48,而哌拉西林为 0.26。
本研究表明,头孢洛扎在给予头孢洛扎/他唑巴坦后很好地渗透到 ELF 中。