Canepa Paolo, Gregurec Danijela, Liessi Nara, Rotondi Silvia Maria Cristina, Moya Sergio Enrique, Millo Enrico, Canepa Maurizio, Cavalleri Ornella
Dipartimento di Fisica and OPTMATLAB, Università di Genova, Via Dodecaneso 33, 16146 Genova, Italy.
Department of Chemistry and Pharmacy, Chair of Aroma and Smell Research, Friedrich-Alexander-Universität Erlangen-Nürnberg, Schlossplatz 4, 91054 Erlangen, Germany.
Materials (Basel). 2023 Jan 13;16(2):784. doi: 10.3390/ma16020784.
Porous transition metal oxides are widely studied as biocompatible materials for the development of prosthetic implants. Resurfacing the oxide to improve the antibacterial properties of the material is still an open issue, as infections remain a major cause of implant failure. We investigated the functionalization of porous titanium oxide obtained by anodic oxidation with amino acids (Leucine) as a first step to couple antimicrobial peptides to the oxide surface. We adopted a two-step molecular deposition process as follows: self-assembly of aminophosphonates to titanium oxide followed by covalent coupling of Fmoc-Leucine to aminophosphonates. Molecular deposition was investigated step-by-step by Atomic Force Microscopy (AFM) and X-ray Photoemission Spectroscopy (XPS). Since the inherent high roughness of porous titanium hampers the analysis of molecular orientation on the surface, we resorted to parallel experiments on flat titanium oxide thin films. AFM nanoshaving experiments on aminophosphonates deposited on flat TiO indicate the formation of an aminophosphonate monolayer while angle-resolved XPS analysis gives evidence of the formation of an oriented monolayer exposing the amine groups. The availability of the amine groups at the outer interface of the monolayer was confirmed on both flat and porous substrates by the following successful coupling with Fmoc-Leucine, as indicated by high-resolution XPS analysis.
多孔过渡金属氧化物作为用于假体植入物开发的生物相容性材料受到广泛研究。由于感染仍然是植入物失败的主要原因,对氧化物进行表面改性以改善材料的抗菌性能仍是一个未解决的问题。我们研究了通过阳极氧化获得的多孔二氧化钛与氨基酸(亮氨酸)的功能化,这是将抗菌肽偶联到氧化物表面的第一步。我们采用了如下两步分子沉积过程:氨基膦酸盐自组装到二氧化钛上,然后将芴甲氧羰基 - 亮氨酸共价偶联到氨基膦酸盐上。通过原子力显微镜(AFM)和X射线光电子能谱(XPS)逐步研究分子沉积。由于多孔钛固有的高粗糙度阻碍了对表面分子取向的分析,我们在平整的二氧化钛薄膜上进行了平行实验。对沉积在平整TiO上的氨基膦酸盐进行的AFM纳米刮削实验表明形成了氨基膦酸盐单层,而角分辨XPS分析证明形成了暴露胺基的取向单层。如高分辨率XPS分析所示,通过与芴甲氧羰基 - 亮氨酸的后续成功偶联,在平整和多孔基底上均证实了单层外界面处胺基的可用性。