Department of Medicine, Yong Loo Lin School of Medicine, National University of Singapore, Singapore.
Singapore Clinical Research Institute, Singapore.
J Antimicrob Chemother. 2017 Jul 1;72(7):2012-2019. doi: 10.1093/jac/dkx081.
Faropenem has in vitro activity against Mycobacterium tuberculosis (Mtb) and shows synergy with rifampicin. We tested this in a whole-blood bactericidal activity (WBA) trial.
We randomized healthy volunteers to receive a single oral dose of faropenem (600 mg) with amoxicillin/clavulanic acid (500/125 mg) ( n = 8), rifampicin (10 mg/kg) ( n = 14) or the combination rifampicin + faropenem + amoxicillin/clavulanic acid ( n = 14). Blood was drawn at intervals to 8 h post-dose. Drug levels were measured using LC-tandem MS. WBA was measured by inoculating blood samples with Mtb and estimating the change in bacterial cfu after 72 h. Trial registration: ClinicalTrials.gov (NCT02393586).
There was no activity in the faropenem + amoxicillin/clavulanic acid group (cumulative WBA 0.02 Δlog cfu; P = 0.99 versus zero change). There was a suggestion of a trend favouring the rifampicin + faropenem + amoxicillin/clavulanic acid group at 8 h (cumulative WBA -0.19 ± 0.03 and -0.26 ± 0.03 Δlog cfu in the rifampicin and rifampicin + faropenem + amoxicillin/clavulanic acid groups, respectively; P = 0.180), which was significant in the first hour post-dose ( P = 0.032). Faropenem C max and AUC were 5.4 mg/L and 16.2 mg·h/L, respectively, and MIC for Mtb H37Rv was 5-10 mg/L.
Faropenem is not active when used alone, possibly due to inadequate plasma levels relative to MIC. However, there was a suggestion of modest synergy with rifampicin that may merit further testing in clinical trials.
法罗培南在体外对结核分枝杆菌(Mtb)具有活性,并显示出与利福平的协同作用。我们在全血杀菌活性(WBA)试验中对此进行了测试。
我们将健康志愿者随机分为三组,分别接受单次口服剂量的法罗培南(600mg)联合阿莫西林/克拉维酸(500/125mg)(n=8)、利福平(10mg/kg)(n=14)或利福平+法罗培南+阿莫西林/克拉维酸联合用药(n=14)。在给药后 8 小时内每隔一段时间抽取血液。使用 LC-串联质谱法测量药物水平。通过将 Mtb 接种到血液样本中并估计 72 小时后细菌 cfu 的变化来测量 WBA。试验注册:ClinicalTrials.gov(NCT02393586)。
法罗培南+阿莫西林/克拉维酸组无活性(累积 WBA 0.02 Δlog cfu;P=0.99 与零变化相比)。利福平+法罗培南+阿莫西林/克拉维酸组在 8 小时时有一个趋势倾向于有利(累积 WBA-0.19 ± 0.03 和-0.26 ± 0.03 Δlog cfu 在利福平组和利福平+法罗培南+阿莫西林/克拉维酸组中,分别;P=0.180),这在给药后第一个小时是显著的(P=0.032)。法罗培南的 C max 和 AUC 分别为 5.4mg/L 和 16.2mg·h/L,Mtb H37Rv 的 MIC 为 5-10mg/L。
法罗培南单独使用时没有活性,可能是由于相对于 MIC 的血浆水平不足。然而,与利福平有适度的协同作用,这可能值得在临床试验中进一步测试。