Debiopharm International SA, Lausanne, Switzerland
Debiopharm International SA, Lausanne, Switzerland.
Antimicrob Agents Chemother. 2019 Feb 26;63(3). doi: 10.1128/AAC.01669-18. Print 2019 Mar.
Afabicin (formerly Debio 1450, AFN-1720) is a prodrug of afabicin desphosphono (Debio 1452, AFN-1252), a novel antibiotic in development which targets the staphylococcal enoyl-acyl carrier protein reductase (FabI) and exhibits selective potent antibacterial activity against staphylococcal species, including methicillin-resistant As part of clinical development in bone and joint infections, a distribution study in bone was performed in 17 patients who underwent elective hip replacement surgery. Patients received 3 doses of 240 mg afabicin orally (every 12 h) at various time points before surgery. Afabicin desphosphono concentrations were measured by liquid chromatography-tandem mass spectrometry in plasma, cortical bone, cancellous bone, bone marrow, soft tissue, and synovial fluid collected during surgery at 2, 4, 6, or 12 h after the third afabicin dose. The study showed good penetration of afabicin desphosphono into bone tissues, with mean area under the curve ratios for cortical bone-, cancellous bone-, bone marrow-, soft tissue-, and synovial fluid-to-total plasma concentrations of 0.21, 0.40, 0.32, 0.35, and 0.61, respectively. When accounting for the free fraction in plasma (2%) and synovial fluid (9.4%), the mean ratio was 2.88, which is indicative of excellent penetration and which showed that the afabicin desphosphono concentration was beyond the MIC of over the complete dosing interval. These findings, along with preclinical efficacy data, clinical efficacy data for skin and soft tissue staphylococcal infection, the availability of both intravenous and oral formulations, and potential advantages over broad-spectrum antibiotics for the treatment of staphylococcal bone or joint infections, support the clinical development of afabicin for bone and joint infections. (This study has been registered at ClinicalTrials.gov under identifier NCT02726438.).
阿法非宾(前身为 Debio 1450,AFN-1720)是一种新型抗生素阿法非宾去膦酸酯(Debio 1452,AFN-1252)的前体药物,该抗生素的作用靶点是葡萄球菌烯酰基辅酶 A 还原酶(FabI),对葡萄球菌属具有选择性的强大抗菌活性,包括耐甲氧西林金黄色葡萄球菌。
作为骨和关节感染临床开发的一部分,在 17 名接受择期髋关节置换手术的患者中进行了骨分布研究。患者在手术前的不同时间点接受了 3 次 240mg 阿法非宾口服(每 12 小时 1 次)。在第三次阿法非宾给药后 2、4、6 或 12 小时,通过液相色谱-串联质谱法测量手术中收集的血浆、皮质骨、松质骨、骨髓、软组织和滑液中的阿法非宾去膦酸酯浓度。
该研究表明阿法非宾去膦酸酯很好地渗透到骨组织中,皮质骨、松质骨、骨髓、软组织和滑液与总血浆浓度的平均曲线下面积比分别为 0.21、0.40、0.32、0.35 和 0.61。当考虑到血浆(2%)和滑液(9.4%)中的游离分数时,平均比值为 2.88,这表明具有极好的穿透性,并且表明阿法非宾去膦酸酯的浓度超过了整个给药间隔的 MIC90。
这些发现,加上临床前疗效数据、皮肤和软组织金黄色葡萄球菌感染的临床疗效数据、静脉内和口服制剂的可用性以及在治疗金黄色葡萄球菌骨或关节感染方面相对于广谱抗生素的潜在优势,支持阿法非宾在骨和关节感染方面的临床开发。(这项研究已在 ClinicalTrials.gov 上注册,登记号为 NCT02726438。)