Rodvold Keith A, Gotfried Mark H, Sabato Philip, Henkel Tim, McGovern Paul C
University of Illinois Chicago, Chicago, Illinois, USA.
Pulmonary Associates, Phoenix, Arizona, USA.
Antimicrob Agents Chemother. 2025 Jul 2;69(7):e0049325. doi: 10.1128/aac.00493-25. Epub 2025 Jun 6.
Cefepime-taniborbactam is being developed for the treatment of serious multidrug-resistant (MDR) Gram-negative bacterial infections. This study determined and compared plasma and epithelial lining fluid (ELF) concentrations of cefepime and taniborbactam in 30 healthy adult participants. The dosing regimen was 2 g cefepime/0.5 g taniborbactam administered as a 4 h intravenous infusion every 8 h for a total of six doses. Mean plasma and ELF concentration values with the four aspirates at each bronchoalveolar lavage (BAL) sampling time (1, 3, 4.25, 5, 6, and 8 h) were used to estimate the area under the concentration-time curve (AUC). The mean AUC values of unbound plasma concentrations of cefepime and taniborbactam were 262.2 and 84.77 µg·h/mL, respectively. The drug penetration ratios of ELF to unbound plasma concentrations (DPR) were based on the AUC values of six different BAL aspirate calculations: single aspirates (for the first, second, third, and fourth BAL sample) and pooled aspirates (BAL samples 2+3+4 and 1+2+3+4). The AUC values for ELF for individual and pooled aspirates ranged from 51.62 to 97.86 µg·h/mL for cefepime and 13.14 to 21.69 µg·h/mL for taniborbactam. The DPR ranged from 0.197 to 0.373 for cefepime and 0.153 to 0.253 for taniborbactam and was dependent on which aspirate of recovered BAL fluid was used. The highest and lowest values of AUC values for ELF and DPR for cefepime and taniborbactam were observed with aspirate 1 and aspirate 4, respectively. These results support further consideration of cefepime-taniborbactam as a potential treatment for bacterial pneumonia caused by susceptible MDR Gram-negative pathogens.CLINICAL TRIALSThis study is registered with ClinicalTrials.gov as NCT04951505.
头孢吡肟-他尼硼巴坦正在研发用于治疗严重多重耐药(MDR)革兰氏阴性菌感染。本研究测定并比较了30名健康成年参与者中头孢吡肟和他尼硼巴坦的血浆浓度及上皮衬液(ELF)浓度。给药方案为每8小时静脉输注2克头孢吡肟/0.5克他尼硼巴坦,持续4小时,共六剂。在每个支气管肺泡灌洗(BAL)采样时间(1、3、4.25、5、6和8小时)采集的四次样本的平均血浆和ELF浓度值用于估计浓度-时间曲线下面积(AUC)。头孢吡肟和他尼硼巴坦未结合血浆浓度的平均AUC值分别为262.2和84.77µg·h/mL。ELF与未结合血浆浓度的药物渗透比(DPR)基于六种不同BAL吸出物计算的AUC值:单次吸出物(用于第一次、第二次、第三次和第四次BAL样本)和合并吸出物(BAL样本2+3+4和1+2+3+4)。头孢吡肟的ELF个体和合并吸出物的AUC值范围为51.62至97.86µg·h/mL,他尼硼巴坦为13.14至21.69µg·h/mL。头孢吡肟的DPR范围为0.197至0.373,他尼硼巴坦为0.153至0.253,且取决于使用的回收BAL液吸出物。头孢吡肟和他尼硼巴坦的ELF和DPR的AUC值最高和最低值分别在吸出物1和吸出物4中观察到。这些结果支持进一步考虑将头孢吡肟-他尼硼巴坦作为由敏感MDR革兰氏阴性病原体引起的细菌性肺炎的潜在治疗方法。临床试验本研究已在ClinicalTrials.gov注册,注册号为NCT04951505。