Filipov Emil, Angelova Liliya, Vig Sanjana, Fernandes Maria Helena, Moreau Gerard, Lasgorceix Marie, Buchvarov Ivan, Daskalova Albena
Institute of Electronics, Bulgarian Academy of Sciences, 72 Tzarigradsko Shousse Blvd., 1784 Sofia, Bulgaria.
Faculdade de Medicina Dentaria, Universidade do Porto, Rua Dr. Manuel Pereira da Silva, 4200-393 Porto, Portugal.
Polymers (Basel). 2022 Jun 12;14(12):2382. doi: 10.3390/polym14122382.
Developing antimicrobial surfaces that combat implant-associated infections while promoting host cell response is a key strategy for improving current therapies for orthopaedic injuries. In this paper, we present the application of ultra-short laser irradiation for patterning the surface of a 3D biodegradable synthetic polymer in order to affect the adhesion and proliferation of bone cells and reject bacterial cells. The surfaces of 3D-printed polycaprolactone (PCL) scaffolds were processed with a femtosecond laser (λ = 800 nm; τ = 130 fs) for the production of patterns resembling microchannels or microprotrusions. MG63 osteoblastic cells, as well as and , were cultured on fs-laser-treated samples. Their attachment, proliferation, and metabolic activity were monitored via colorimetric assays and scanning electron microscopy. The microchannels improved the wettability, stimulating the attachment, spreading, and proliferation of osteoblastic cells. The same topography induced cell-pattern orientation and promoted the expression of alkaline phosphatase in cells growing in an osteogenic medium. The microchannels exerted an inhibitory effect on as after 48 h cells appeared shrunk and disrupted. In comparison, formed an abundant biofilm over both the laser-treated and control samples; however, the film was dense and adhesive on the control PCL but unattached over the microchannels.
开发既能对抗植入相关感染又能促进宿主细胞反应的抗菌表面,是改善当前骨科损伤治疗方法的关键策略。在本文中,我们展示了超短激光辐照在3D可生物降解合成聚合物表面进行图案化处理的应用,以影响骨细胞的粘附和增殖并排斥细菌细胞。用飞秒激光(λ = 800 nm;τ = 130 fs)对3D打印的聚己内酯(PCL)支架表面进行处理,以制作类似微通道或微突起的图案。将MG63成骨细胞以及其他细胞接种在飞秒激光处理过的样品上。通过比色测定法和扫描电子显微镜监测它们的附着、增殖和代谢活性。微通道改善了润湿性,刺激了成骨细胞的附着、铺展和增殖。相同的形貌诱导细胞图案定向,并促进在成骨培养基中生长的细胞中碱性磷酸酶的表达。微通道对细菌产生抑制作用,因为48小时后细胞出现收缩和破裂。相比之下,细菌在激光处理过的样品和对照样品上都形成了丰富的生物膜;然而,该膜在对照PCL上致密且有粘性,而在微通道上则未附着。