Pennone Vincenzo, Meogrossi Giada, Carenzi Giacomo, Sarlah David, Biagiotti Marco, Lovati Arianna B
Cell and Tissue Engineering Laboratory, IRCCS Istituto Ortopedico Galeazzi, via Cristina Belgioioso 173, 20157 Milan, Italy.
Fondazione Istituto Insubrico Ricerca per la Vita, via Lepetit 34, 21040 Gerenzano, Italy.
Int J Mol Sci. 2025 Aug 12;26(16):7775. doi: 10.3390/ijms26167775.
species are often the cause of implant-related infections, posing a significant clinical challenge in orthopedics. Antimicrobial peptides (AMPs) like LL-37-derived FK-16 and GF-17 offer promising alternatives to conventional antibiotics; however, they require suitable delivery systems to overcome rapid degradation. The aim of this study was to develop and evaluate silk fibroin (SF) and osteoinductive peptide-enriched silk fibroin (PSF) sponges that can be used locally for FK-16 and GF-17 delivery. Two concentrations of FK-16 or GF-17 were loaded into SF and PSF sponges. Swelling behavior and AMP release profiles were analyzed for 72 h. Time-kill assays were conducted on MRSE and MRSA clinical strains to assess antimicrobial activity. FK-16 released quickly (>90% within 24 h) and then maintained a stable plateau from both SF and PSF matrices, which was associated with bactericidal activity against MRSE strains. In contrast, the release efficiency of GF-17 was lower and did not achieve significant antimicrobial effects. Neither peptide exhibited effective activity against MRSA under the tested conditions. PSF sponges showed higher swelling and enhanced FK-16-mediated antibacterial performance compared to SF counterparts. FK-16-loaded PSF sponges are a promising biomaterial for treating local orthopedic infections related to MRSE. The findings underscore the significance of peptide-matrix interactions in determining therapeutic outcomes and suggest the need for more in vivo evaluation of AMP-functionalized PSF scaffolds.
物种通常是植入物相关感染的原因,在骨科领域构成了重大的临床挑战。像源自LL-37的FK-16和GF-17这样的抗菌肽为传统抗生素提供了有前景的替代方案;然而,它们需要合适的递送系统来克服快速降解的问题。本研究的目的是开发并评估可用于局部递送FK-16和GF-17的丝素蛋白(SF)海绵以及富含骨诱导肽的丝素蛋白(PSF)海绵。将两种浓度的FK-16或GF-17加载到SF和PSF海绵中。分析了72小时内的溶胀行为和抗菌肽释放曲线。对耐甲氧西林表皮葡萄球菌(MRSE)和耐甲氧西林金黄色葡萄球菌(MRSA)临床菌株进行了时间杀菌试验,以评估抗菌活性。FK-16从SF和PSF基质中快速释放(24小时内>90%),然后保持稳定的平台期,这与对MRSE菌株的杀菌活性相关。相比之下,GF-17的释放效率较低,未达到显著的抗菌效果。在测试条件下,两种肽对MRSA均未表现出有效活性。与SF海绵相比,PSF海绵表现出更高的溶胀度和增强的FK-16介导的抗菌性能。负载FK-16的PSF海绵是治疗与MRSE相关的局部骨科感染的一种有前景的生物材料。这些发现强调了肽-基质相互作用在决定治疗结果中的重要性,并表明需要对AMP功能化的PSF支架进行更多的体内评估。