Coppola Guglielmo Attilio, Onsea Jolien, Moriarty T Fintan, Nehrbass Dirk, Constant Caroline, Zeiter Stephan, Aktan Merve Kübra, Braem Annabel, Van der Eycken Erik V, Steenackers Hans P, Metsemakers Willem-Jan
KU Leuven - Department of Chemistry, Laboratory for Organic & Microwave-Assisted Chemistry (LOMAC), Leuven, Belgium.
KU Leuven - Department of Microbial and Molecular Systems, Centre of Microbial and Plant Genetics (CMPG), Leuven, Belgium.
Front Microbiol. 2021 Apr 21;12:658521. doi: 10.3389/fmicb.2021.658521. eCollection 2021.
Orthopedic device-related infections remain a serious challenge to treat. Central to these infections are bacterial biofilms that form on the orthopedic implant itself. These biofilms shield the bacteria from the host immune system and most common antibiotic drugs, which renders them essentially antibiotic-tolerant. There is an urgent clinical need for novel strategies to prevent these serious infections that do not involve conventional antibiotics. Recently, a novel antibiofilm coating for titanium surfaces was developed based on 5-(4-bromophenyl)--cyclopentyl-1-octyl-1-imidazol-2-amine as an active biofilm inhibitor. In the current study we present an optimized coating protocol that allowed for a 5-fold higher load of this active compound, whilst shortening the manufacturing process. When applied to titanium disks, the newly optimized coating was resilient to the most common sterilization procedures and it induced a 1 log reduction in biofilm cells of a clinical isolate (JAR060131) , without affecting the planktonic phase. Moreover, the antibiofilm effect of the coating in combination with the antibiotic cefuroxime was higher than cefuroxime treatment alone. Furthermore, the coating was successfully applied to a human-scale fracture fixation device resulting in a loading that was comparable to the titanium disk model. Finally, an biocompatibility and healing study in a rabbit osteotomy model indicated that these coated implants did not negatively affect fracture healing or osteointegration. These findings put our technology one step closer to clinical trials, confirming its potential in fighting orthopedic infections without compromising healing.
骨科器械相关感染的治疗仍然是一项严峻挑战。这些感染的核心是在骨科植入物本身形成的细菌生物膜。这些生物膜保护细菌免受宿主免疫系统和大多数常见抗生素药物的影响,使其基本上具有抗生素耐受性。迫切需要新的策略来预防这些不涉及传统抗生素的严重感染。最近,基于5-(4-溴苯基)-1-环戊基-1-辛基-1-咪唑-2-胺作为一种活性生物膜抑制剂,开发了一种用于钛表面的新型抗生物膜涂层。在本研究中,我们提出了一种优化的涂层方案,该方案可使这种活性化合物的负载量提高5倍,同时缩短制造过程。当应用于钛盘时,新优化的涂层对最常见的灭菌程序具有耐受性,并且它能使临床分离株(JAR060131)的生物膜细胞减少1个对数,而不影响浮游菌阶段。此外,该涂层与抗生素头孢呋辛联合使用的抗生物膜效果高于单独使用头孢呋辛治疗。此外,该涂层已成功应用于人体规模的骨折固定装置,其负载量与钛盘模型相当。最后,在兔截骨模型中的生物相容性和愈合研究表明,这些涂层植入物不会对骨折愈合或骨整合产生负面影响。这些发现使我们的技术向临床试验又迈进了一步,证实了其在不影响愈合的情况下对抗骨科感染的潜力。