University of Illinois at Chicago, Chicago, Illinois, USA
University of Illinois at Chicago, Chicago, Illinois, USA.
Antimicrob Agents Chemother. 2018 Jul 27;62(8). doi: 10.1128/AAC.00682-18. Print 2018 Aug.
WCK 5222 is a combination of cefepime and the novel β-lactam enhancer zidebactam being developed for the treatment of serious Gram-negative bacterial infections. The objective of this study was to compare plasma (total), epithelial lining fluid (ELF), and alveolar macrophage (AM) concentrations of cefepime and zidebactam in healthy adult subjects. The WCK 5222 dosing regimen was 2 g cefepime/1 g zidebactam administered as a 1-h intravenous infusion every 8 h for a total of 7 doses. Subjects were assigned to one bronchoalveolar lavage (BAL) sampling time at 0.5, 1.25, 3, 6, 8, or 10 h after the seventh dose. Noncompartmental pharmacokinetic parameters were determined from serial plasma concentrations collected over 8-hour and 10-hour intervals following the first and seventh doses, respectively. Penetration ratios were calculated from the area under the plasma concentration-time curve from 0 to 8 h (AUC) for plasma, ELF, and AM using mean and median concentrations at each BAL sampling time. The plasma maximum concentration of drug () and AUC values of cefepime and zidebactam increased by 8% to 9% after the seventh versus the first dose of WCK 5222. The respective AUC values based on mean concentrations of cefepime and zidebactam in ELF were 127.9 and 52.0 mg · h/liter, and 87.9 and 13.2 mg · h/liter in AM. The ELF to total plasma penetration ratios of cefepime and zidebactam based on mean AUC values were 0.39 and 0.38, respectively. The AM to total plasma ratios were 0.27 and 0.10, respectively. The observed plasma, ELF, and AM concentrations of cefepime and zidebactam support studies of WCK 5222 for treatment of pneumonia caused by susceptible pathogens.
WCK 5222 是头孢吡肟和新型β-内酰胺增强剂齐他培南的组合药物,用于治疗严重的革兰氏阴性细菌感染。本研究的目的是比较健康成年受试者中头孢吡肟和齐他培南的血浆(总)、上皮衬液(ELF)和肺泡巨噬细胞(AM)浓度。WCK 5222 的给药方案为每 8 小时静脉输注 1 小时,每次 2 g 头孢吡肟/1 g 齐他培南,共 7 剂。在第 7 剂后 0.5、1.25、3、6、8 或 10 小时,受试者被分配进行一次支气管肺泡灌洗(BAL)采样。分别从第一次和第七次剂量后 8 小时和 10 小时的连续血浆浓度中确定非房室药代动力学参数。使用每个 BAL 采样时间的平均和中位数浓度,从 0 至 8 小时(AUC)的血浆、ELF 和 AM 的血浆浓度-时间曲线下面积(AUC)计算渗透比。WCK 5222 第 7 剂与第 1 剂相比,药物的血浆最大浓度()和头孢吡肟和齐他培南的 AUC 值分别增加了 8%至 9%。基于 ELF 中头孢吡肟和齐他培南的平均浓度的 AUC 值分别为 127.9 和 52.0 mg·h/L,以及 AM 中的 87.9 和 13.2 mg·h/L。基于平均 AUC 值的头孢吡肟和齐他培南的 ELF 与总血浆渗透比分别为 0.39 和 0.38。AM 与总血浆的比值分别为 0.27 和 0.10。观察到的头孢吡肟和齐他培南的血浆、ELF 和 AM 浓度支持 WCK 5222 治疗敏感病原体引起的肺炎的研究。