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2
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本文引用的文献

1
Comparison of piperacillin exposure in the lungs of critically ill patients and healthy volunteers.比较危重症患者和健康志愿者肺部哌拉西林的暴露情况。
J Antimicrob Chemother. 2018 May 1;73(5):1340-1347. doi: 10.1093/jac/dkx541.
2
Intrapulmonary Pharmacokinetics of Relebactam, a Novel β-Lactamase Inhibitor, Dosed in Combination with Imipenem-Cilastatin in Healthy Subjects.健康受试者中新型β-内酰胺酶抑制剂雷巴他定与亚胺培南-西司他丁联合给药的肺内药代动力学。
Antimicrob Agents Chemother. 2018 Feb 23;62(3). doi: 10.1128/AAC.01411-17. Print 2018 Mar.
3
Considerations for effect site pharmacokinetics to estimate drug exposure: concentrations of antibiotics in the lung.考虑药代动力学效应部位以估计药物暴露:肺中的抗生素浓度。
Curr Opin Pharmacol. 2017 Oct;36:114-123. doi: 10.1016/j.coph.2017.09.019. Epub 2017 Oct 31.
4
Potent β-Lactam Enhancer Activity of Zidebactam and WCK 5153 against Acinetobacter baumannii, Including Carbapenemase-Producing Clinical Isolates.Zidebactam 和 WCK 5153 对鲍曼不动杆菌的强效β-内酰胺增强活性,包括产碳青霉烯酶的临床分离株。
Antimicrob Agents Chemother. 2017 Oct 24;61(11). doi: 10.1128/AAC.01238-17. Print 2017 Nov.
5
Antibacterial drug development program successes and failures: a pharmacometric explanation.抗菌药物研发项目的成败:药物计量学解释。
Curr Opin Pharmacol. 2017 Oct;36:1-7. doi: 10.1016/j.coph.2017.06.002. Epub 2017 Jul 5.
6
WCK 5222 (cefepime/zidebactam) antimicrobial activity tested against Gram-negative organisms producing clinically relevant β-lactamases.WCK 5222(头孢吡肟/齐地卡南)针对产生具有临床相关性β-内酰胺酶的革兰氏阴性菌的抗菌活性测试。
J Antimicrob Chemother. 2017 Jun 1;72(6):1696-1703. doi: 10.1093/jac/dkx050.
7
WCK 5107 (Zidebactam) and WCK 5153 Are Novel Inhibitors of PBP2 Showing Potent "β-Lactam Enhancer" Activity against Pseudomonas aeruginosa, Including Multidrug-Resistant Metallo-β-Lactamase-Producing High-Risk Clones.WCK 5107(齐德巴坦)和WCK 5153是新型PBP2抑制剂,对铜绿假单胞菌表现出强大的“β-内酰胺增强剂”活性,包括产多重耐药金属β-内酰胺酶的高风险克隆株。
Antimicrob Agents Chemother. 2017 May 24;61(6). doi: 10.1128/AAC.02529-16. Print 2017 Jun.
8
WCK 5222 (Cefepime-Zidebactam) Antimicrobial Activity against Clinical Isolates of Gram-Negative Bacteria Collected Worldwide in 2015.WCK 5222(头孢吡肟-齐地巴坦)对2015年全球收集的革兰氏阴性菌临床分离株的抗菌活性。
Antimicrob Agents Chemother. 2017 Apr 24;61(5). doi: 10.1128/AAC.00072-17. Print 2017 May.
9
What we may expect from novel antibacterial agents in the pipeline with respect to resistance and pharmacodynamic principles.就耐药性和药效学原理而言,我们对正在研发的新型抗菌药物有何期待。
J Pharmacokinet Pharmacodyn. 2017 Apr;44(2):113-132. doi: 10.1007/s10928-017-9506-4. Epub 2017 Feb 4.
10
In vitro activity of cefepime/zidebactam (WCK 5222) against Gram-negative bacteria.头孢吡肟/齐他西酮(WCK 5222)对革兰氏阴性菌的体外活性
J Antimicrob Chemother. 2017 May 1;72(5):1373-1385. doi: 10.1093/jac/dkw593.

健康成年受试者静脉给予 WCK 5222 后头孢吡肟和齐多夫定的血浆和肺内浓度。

Plasma and Intrapulmonary Concentrations of Cefepime and Zidebactam following Intravenous Administration of WCK 5222 to Healthy Adult Subjects.

机构信息

University of Illinois at Chicago, Chicago, Illinois, USA

University of Illinois at Chicago, Chicago, Illinois, USA.

出版信息

Antimicrob Agents Chemother. 2018 Jul 27;62(8). doi: 10.1128/AAC.00682-18. Print 2018 Aug.

DOI:10.1128/AAC.00682-18
PMID:29784852
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6105785/
Abstract

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.

摘要

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。