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负载LL-37衍生肽的丝素蛋白基海绵用于控制骨科感染的研究进展

Development of Silk Fibroin-Based Sponges Loaded with LL-37-Derived Peptides for the Control of Orthopedic Infections.

作者信息

Pennone Vincenzo, Meogrossi Giada, Carenzi Giacomo, Sarlah David, Biagiotti Marco, Lovati Arianna B

机构信息

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.

出版信息

Int J Mol Sci. 2025 Aug 12;26(16):7775. doi: 10.3390/ijms26167775.

Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/43c4/12386548/fb6f263fde68/ijms-26-07775-g001.jpg

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