Fontelo R, Soares da Costa D, Reis R L, Novoa-Carballal R, Pashkuleva I
3B's Research Group, I3Bs - Research Institute on Biomaterials, Biodegradables and Biomimetics, University of Minho, Headquarters of the European Institute of Excellence on Tissue Engineering and Regenerative Medicine, AvePark, Parque de Ciência e Tecnologia, Zona Industrial da Gandra, 4805-017 Barco, Guimarães, Portugal; ICVS/3B's-PT Government Associate Laboratory, Braga Guimarães, Portugal.
3B's Research Group, I3Bs - Research Institute on Biomaterials, Biodegradables and Biomimetics, University of Minho, Headquarters of the European Institute of Excellence on Tissue Engineering and Regenerative Medicine, AvePark, Parque de Ciência e Tecnologia, Zona Industrial da Gandra, 4805-017 Barco, Guimarães, Portugal; ICVS/3B's-PT Government Associate Laboratory, Braga Guimarães, Portugal; The Discoveries Centre for Regenerative and Precision Medicine, Headquarters at University of Minho, Avepark, 4805-017 Barco, Guimarães, Portugal.
Acta Biomater. 2020 Aug;112:174-181. doi: 10.1016/j.actbio.2020.06.003. Epub 2020 Jun 7.
We describe the bactericidal capacity of nanopatterned surfaces created by self-assembly of block copolymers. Distinct nanotopographies were generated by spin-coating with polystyrene-block-poly(2-vinylpyridine) (PS-b-P2VP) followed by solvent vapor annealing. We demonstrate that the bactericidal efficiency of the developed coatings depends on the morphology and the chemistry of the surface: cylindrical nanotopographies presenting both blocks at the surface have stronger bactericidal effect on Escherichia coli than micellar patterns with only PS exposed at the surface. The identified mechanism of bacterial death is a mechanical stress exerted by the nanostructures on the cell-wall. Moreover, the developed nanopatterns are not cytotoxic, which makes them an excellent option for coating of implantable materials and devices. The proposed approach represents an efficient tool in the fight against bacteria, which acts via compromising the bacterial wall integrity. STATEMENT OF SIGNIFICANCE: Bacterial infections represent an important risk during biomaterial implantation in surgeries due to the increase of antibiotic resistance. Bactericidal surfaces are a promising solution to avoid the use of antibiotics, but most of those systems do not allow mammalian cell survival. Nanopatterned silicon surfaces have demonstrated to be simultaneously bactericidal and allow mammalian cell culture but are made by physical methods (e.g. plasma etching) applicable to few materials and small surfaces. In this article we show that block copolymer self-assembly can be used to develop surfaces that kill bacteria (E. coli) but do not harm mammalian cells. Block copolymer self-assembly has the advantage of being applicable to many different types of substrates and large surface areas.
我们描述了通过嵌段共聚物自组装形成的纳米图案化表面的杀菌能力。通过旋涂聚苯乙烯-嵌段-聚(2-乙烯基吡啶)(PS-b-P2VP)并随后进行溶剂蒸汽退火来产生不同的纳米拓扑结构。我们证明,所开发涂层的杀菌效率取决于表面的形态和化学性质:表面呈现两种嵌段的圆柱形纳米拓扑结构对大肠杆菌的杀菌作用比仅表面暴露有PS的胶束图案更强。确定的细菌死亡机制是纳米结构对细胞壁施加的机械应力。此外,所开发的纳米图案没有细胞毒性,这使其成为用于涂覆可植入材料和装置的极佳选择。所提出的方法是对抗细菌的一种有效工具,其通过破坏细菌壁完整性来发挥作用。重要性声明:由于抗生素耐药性的增加,细菌感染在手术中生物材料植入期间是一个重要风险。杀菌表面是避免使用抗生素的一种有前途的解决方案,但大多数此类系统不允许哺乳动物细胞存活。纳米图案化硅表面已证明具有同时杀菌和允许哺乳动物细胞培养的能力,但它是通过物理方法(例如等离子体蚀刻)制成的,适用于少数材料和小表面。在本文中,我们表明嵌段共聚物自组装可用于开发能够杀死细菌(大肠杆菌)但不伤害哺乳动物细胞的表面。嵌段共聚物自组装的优点是适用于许多不同类型的基材和大面积表面。