Yao Yicun, Lin Peifen, Ye Dongping, Miao Haixiong, Cao Lin, Zhang Peng, Xu Jiake, Dai Libing
Department of Orthopedics, Guangzhou Red Cross Hospital, Guangzhou Red Cross Hospital of Jinan University, Guangzhou, Guangdong, 510220, People's Republic of China.
Guangzhou Institute of Traumatic Surgery, Guangzhou Red Cross Hospital, Guangzhou Red Cross Hospital of Jinan University, Guangzhou, Guangdong, 510220, People's Republic of China.
Int J Nanomedicine. 2025 Mar 24;20:3749-3764. doi: 10.2147/IJN.S493754. eCollection 2025.
This study explored constructing silver-loaded titanium dioxide nanotube (TiO NT) arrays on titanium surfaces using anodic oxidation combined with ion implantation. We assessed the cytocompatibility, antibacterial properties, and osteogenic potential of these silver-loaded TiO NT arrays, along with the underlying mechanisms.
We utilized anodization to create TiO NT arrays and employed ion implantation to load silver ions, categorizing samples into groups NT-Ag-II-L, NT-Ag-II-M, and NT-Ag-II-H based on different Ag ion dosages. Characterization was performed via scanning electron microscopy (SEM). We evaluated cell compatibility and assessed the antimicrobial performance and Ag ion release profiles. The osteogenic ability of the samples was measured, and the effects on ERK5 and osteogenesis-related factors were analyzed. To clarify the role of ERK5 in osteogenesis, we inhibited the ERK5 pathway using BIX02188 and subsequently re-evaluated osteogenic capacity in co-cultured cells.
SEM analysis showed that in the NT-Ag-II-M group, Ag ions exhibited a flake-like distribution atop the TiO NTs, while NT-Ag-II-L and NT-Ag-II-H groups presented clustered grid structures. Energy-filtered transmission electron microscopy (EFTEM) confirmed orderly Ag ion arrangements within the lumens of the nanotubes. Notably, the silver-loaded TiO NT arrays did not inhibit MC3T3-E1 cell proliferation and enhanced early cellular adhesion. All samples displayed significant antimicrobial activity initially, which decreased after seven days; however, Ag ion release decreased gradually over the first 14 days before stabilizing. Additionally, the samples increased alkaline phosphatase activity, collagen secretion, and extracellular matrix mineralization, up-regulating ERK5 and other osteogenic factors. Inhibition of the ERK5 pathway suppressed the osteogenic capabilities of the samples.
Anodization and ion implantation successfully produced silver-loaded TiO NT arrays on titanium surfaces, demonstrating no cytotoxicity, sustained antimicrobial properties, and enhanced osteogenic potential. The antimicrobial effect relates to silver ion release, whereas osteogenesis is promoted by ERK5 signaling triggered by silver ions.
本研究探索通过阳极氧化结合离子注入在钛表面构建载银二氧化钛纳米管(TiO NT)阵列。我们评估了这些载银TiO NT阵列的细胞相容性、抗菌性能和成骨潜力,以及潜在机制。
我们利用阳极氧化创建TiO NT阵列,并采用离子注入加载银离子,根据不同的银离子剂量将样品分为NT-Ag-II-L、NT-Ag-II-M和NT-Ag-II-H组。通过扫描电子显微镜(SEM)进行表征。我们评估了细胞相容性,评估了抗菌性能和银离子释放曲线。测量了样品的成骨能力,并分析了对ERK5和成骨相关因子的影响。为了阐明ERK5在成骨中的作用,我们使用BIX02188抑制ERK5通路,随后重新评估共培养细胞中的成骨能力。
SEM分析表明,在NT-Ag-II-M组中,银离子在TiO NTs顶部呈片状分布,而NT-Ag-II-L和NT-Ag-II-H组呈现聚集的网格结构。能量过滤透射电子显微镜(EFTEM)证实了纳米管腔内银离子的有序排列。值得注意的是,载银TiO NT阵列没有抑制MC3T3-E1细胞增殖,并增强了早期细胞粘附。所有样品最初均显示出显著的抗菌活性,七天后活性下降;然而,银离子释放在最初的14天内逐渐减少,然后趋于稳定。此外,样品增加了碱性磷酸酶活性、胶原蛋白分泌和细胞外基质矿化,上调了ERK5和其他成骨因子。抑制ERK5通路抑制了样品的成骨能力。
阳极氧化和离子注入成功地在钛表面制备了载银TiO NT阵列,显示出无细胞毒性、持续的抗菌性能和增强的成骨潜力。抗菌作用与银离子释放有关,而成骨是由银离子触发的ERK5信号传导促进的。