Universidade Estadual Paulista - UNESP, Faculdade de Odontologia de Araraquara, Departamento de Diagnóstico e Cirurgia, Araraquara, São Paulo, Brasil.
Extremus Smart Surface, São Carlos, São Paulo, Brasil.
J Appl Oral Sci. 2024 Sep 16;32:e20240144. doi: 10.1590/1678-7757-2024-0144. eCollection 2024.
This study aimed to investigate the osseointegration of titanium (Ti) implants with micro-nano textured surfaces functionalized with strontium additions (Sr) in a pre-clinical rat tibia model.
Ti commercially pure (cp-Ti) implants were installed bilaterally in the tibia of 64 Holtzman rats, divided into four experimental groups (n=16/group): (1) Machined surface - control (C); (2) Micro-nano textured surface treatment (MN); (3) Micro-nano textured surface with Sr2+ addition (MNSr); and (4) Micro-nano textured surface with a higher complementary addition of Sr2+ (MNSr+). In total, two experimental euthanasia periods were assessed at 15 and 45 days (n=8/period). The tibia was subjected to micro-computed tomography (μ-CT), histomorphometry with the EXAKT system, removal torque (TR) testing, and gene expression analysis by PCR-Array of 84 osteogenic markers. Gene expression and protein production of bone markers were performed in an in vitro model with MC3T3-E1 cells. The surface characteristics of the implants were evaluated by scanning electron microscopy (SEM), energy-dispersive spectroscopy (EDS), and laser scanning confocal microscopy.
SEM, confocal, and EDS analyses demonstrated the formation of uniform micro-nano textured surfaces in the MN group and Sr addition in the MNSr and MNSr+ groups. TR test indicated greater osseointegration in the 45-day period for treated surfaces. Histological analysis highlighted the benefits of the treatments, especially in cortical bone, in which an increase in bone-implant contact was found in groups MN (15 days) and MNSr (45 days) compared to the control group. Gene expression analysis of osteogenic activity markers showed modulation of various osteogenesis-related genes. According to the in vitro model, RT-qPCR and ELISA demonstrated that the treatments favored gene expression and production of osteoblastic differentiation markers.
Micro-nano textured surface and Sr addition can effectively improve and accelerate implant osseointegration and is, therefore, an attractive approach to modifying titanium implant surfaces with significant potential in clinical practice.
本研究旨在通过临床前大鼠胫骨模型,研究具有锶添加的微纳纹理表面功能化的钛(Ti)植入物的骨整合情况。
将商用纯钛(cp-Ti)植入物双侧植入 64 只霍尔茨曼大鼠的胫骨中,分为四个实验组(n=16/组):(1)机械加工表面-对照(C);(2)微纳纹理表面处理(MN);(3)具有 Sr2+添加的微纳纹理表面(MNSr);和(4)具有更高互补添加 Sr2+的微纳纹理表面(MNSr+)。总共评估了两个实验性安乐死期,分别为 15 天和 45 天(n=8/期)。对胫骨进行微计算机断层扫描(μ-CT)、EXAKT 系统的组织形态计量学、去除扭矩(TR)测试以及 84 种成骨标志物的 PCR-Array 基因表达分析。在 MC3T3-E1 细胞的体外模型中进行了骨标记物的基因表达和蛋白质产生。通过扫描电子显微镜(SEM)、能谱分析(EDS)和激光共聚焦显微镜评估了植入物的表面特性。
SEM、共聚焦和 EDS 分析表明,在 MN 组和 MNSr 和 MNSr+组中形成了均匀的微纳纹理表面和 Sr 添加。TR 测试表明,在处理后的表面上,45 天期间的骨整合更好。组织学分析突出了处理的好处,特别是在皮质骨中,与对照组相比,MN 组(15 天)和 MNSr 组(45 天)的骨-植入物接触增加。成骨活性标志物的基因表达分析表明,各种成骨相关基因的表达发生了变化。根据体外模型,RT-qPCR 和 ELISA 表明,这些处理有利于成骨细胞分化标志物的基因表达和产生。
微纳纹理表面和 Sr 添加可以有效改善和加速植入物的骨整合,因此是一种有吸引力的方法,可以修饰具有临床应用重要潜力的钛植入物表面。