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头孢洛扎他唑巴坦在下肢感染的糖尿病患者和健康成年志愿者中的药代动力学和组织穿透性。

Pharmacokinetics and Tissue Penetration of Ceftolozane-Tazobactam in Diabetic Patients with Lower Limb Infections and Healthy Adult Volunteers.

机构信息

Center for Anti-Infective Research and Development, Hartford Hospital, Hartford, Connecticut, USA.

Hartford Healthcare Medical Group, Podiatric Surgery, Hartford, Connecticut, USA.

出版信息

Antimicrob Agents Chemother. 2017 Nov 22;61(12). doi: 10.1128/AAC.01449-17. Print 2017 Dec.

DOI:10.1128/AAC.01449-17
PMID:28893779
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5700352/
Abstract

Ceftolozane-tazobactam displays potent activity against Gram-negative bacteria that can cause diabetic foot infections (DFI), making it an attractive treatment option when few alternatives exist. The pharmacokinetics and tissue penetration of ceftolozane-tazobactam at 1.5 g every 8 h (q8h) in patients ( = 10) with DFI were compared with those in healthy volunteers ( = 6) using microdialysis. In the patient participants, the median values of the pharmacokinetic parameters for ceftolozane in total plasma were as follows: maximum concentration (), 55.2 μg/ml (range, 40.9 to 169.3 μg/ml); half-life (), 3.5 h (range, 2.3 to 4.7 h); and area under the concentration-time curve (AUC) from time zero to 8 h (AUC), 191.6 μg · h/ml (range, 147.1 to 286.6 μg · h/ml). The median AUC for tissue (AUC; where AUC was the AUC for tissue for ceftolozane)/AUC for plasma for each antibiotic corrected by the fraction of free drug (AUC) was 0.75 (range, 0.35 to 1.00), resulting in a mean free time above 4 μg/ml (the susceptibility breakpoint) in tissue of 99.8% (range, 87.5 to 100%). In the patient participants, the median values of the pharmacokinetic parameters for tazobactam in total plasma were as follows: , 14.2 μg/ml (range, 7.6 to 64.2 μg/ml); , 2.0 h (range, 0.7 to 2.4 h); and AUC, 27.1 μg · h/ml (range, 15.0 to 70.0 μg · h/ml). The AUC (where AUC was the AUC from time zero to the time of the last measureable concentration in tissue for tazobactam)/AUC for tazobactam was 1.18 (range, 0.54 to 1.44). In the healthy volunteers, the median values of the pharmacokinetic parameters for ceftolozane in total plasma were as follows: , 91.5 μg/ml (range, 65.7 to 110.7 μg/ml); , 1.9 h (range, 1.6 to 2.1 h); and AUC, 191.3 μg · h/ml (range, 118.1 to 274.3 μg · h/ml). The median AUC/AUC was 0.87 (range, 0.54 to 2.20), resulting in a mean free time above 4 μg/ml in tissue of 93.8% (range, 87.5 to 100%). In the healthy volunteers, the median values of the pharmacokinetic parameters for tazobactam in total plasma were as follows: , 17.5 μg/ml (range, 15.4 to 27.3 μg/ml); , 0.7 h (range, 0.6 to 0.8 h); and AUC, 22.2 μg · h/ml (range, 19.2 to 36.4 μg · h/ml). The AUC/AUC for tazobactam was 0.85 (range, 0.63 to 2.10). Both ceftolozane and tazobactam penetrated into subcutaneous tissue with exposures similar to those of free drug in plasma in both patients with DFI and healthy volunteers. These data suggest that ceftolozane-tazobactam at 1.5 g q8h can achieve the optimal exposure with activity against susceptible Gram-negative pathogens in the tissue of patients with DFI. (This study has been registered at ClinicalTrials.gov under identifier NCT02620774.).

摘要

头孢洛扎他唑巴坦对引起糖尿病足感染(DFI)的革兰氏阴性菌具有强大的活性,当治疗选择有限时,它是一种有吸引力的治疗选择。使用微透析法比较了 1.5 g 每 8 小时(q8h)在 DFI 患者(n = 10)和健康志愿者(n = 6)中的头孢洛扎他唑巴坦的药代动力学和组织穿透性。在患者参与者中,头孢洛扎他唑巴坦在总血浆中的药代动力学参数的中位数值如下:最大浓度(),55.2 μg/ml(范围,40.9 至 169.3 μg/ml);半衰期(),3.5 h(范围,2.3 至 4.7 h);和从时间 0 到 8 h 的浓度-时间曲线下面积(AUC)(AUC),191.6 μg·h/ml(范围,147.1 至 286.6 μg·h/ml)。抗生素的游离药物分数(AUC)校正后的组织(AUC;其中 AUC 为头孢洛扎他唑巴坦的组织 AUC)/血浆 AUC 的中位数值为 0.75(范围,0.35 至 1.00),导致组织中 4 μg/ml 以上的游离时间平均为 99.8%(范围,87.5% 至 100%)。在患者参与者中,头孢洛扎他唑巴坦在总血浆中的药代动力学参数的中位数值如下:,14.2 μg/ml(范围,7.6 至 64.2 μg/ml);,2.0 h(范围,0.7 至 2.4 h);和 AUC,27.1 μg·h/ml(范围,15.0 至 70.0 μg·h/ml)。AUC(其中 AUC 是从时间 0 到组织中可测量浓度的最后时间的头孢洛扎他唑巴坦的 AUC)/头孢洛扎他唑巴坦的 AUC 的中位数值为 1.18(范围,0.54 至 1.44)。在健康志愿者中,头孢洛扎他唑巴坦在总血浆中的药代动力学参数的中位数值如下:,91.5 μg/ml(范围,65.7 至 110.7 μg/ml);,1.9 h(范围,1.6 至 2.1 h);和 AUC,191.3 μg·h/ml(范围,118.1 至 274.3 μg·h/ml)。AUC/AUC 的中位数值为 0.87(范围,0.54 至 2.20),导致组织中 4 μg/ml 以上的游离时间平均为 93.8%(范围,87.5% 至 100%)。在健康志愿者中,头孢洛扎他唑巴坦在总血浆中的药代动力学参数的中位数值如下:,17.5 μg/ml(范围,15.4 至 27.3 μg/ml);,0.7 h(范围,0.6 至 0.8 h);和 AUC,22.2 μg·h/ml(范围,19.2 至 36.4 μg·h/ml)。头孢洛扎他唑巴坦的 AUC/AUC 为 0.85(范围,0.63 至 2.10)。头孢洛扎他唑巴坦和他唑巴坦均渗透到皮下组织,在 DFI 患者和健康志愿者中,游离药物在血浆中的暴露与组织中的暴露相似。这些数据表明,1.5 g 每 8 小时的头孢洛扎他唑巴坦可以在 DFI 患者的组织中实现对敏感革兰氏阴性病原体的最佳暴露和活性。(本研究已在 ClinicalTrials.gov 上注册,标识符为 NCT02620774。)

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