Göransson A, Arvidsson A, Currie F, Franke-Stenport V, Kjellin P, Mustafa K, Sul Y T, Wennerberg A
Department of Biomaterials, Institute of Surgical Science, Sahlgrenska Academy at Göteborg University, Göteborg, Sweden.
J Biomed Mater Res A. 2009 Mar 15;88(4):1037-47. doi: 10.1002/jbm.a.31911.
The aim of the study was to compare Ca and P formation (CaP) and subsequent bone cell response of a blasted and four different possibly bioactive commercially pure (cp) titanium surfaces; 1. Fluoride etched (Fluoride), 2. Alkali-heat treated (AH), 3. Magnesium ion incorporated anodized (TiMgO), and 4. Nano HA coated and heat treated (nano HA) in vitro. Furthermore, to evaluate the significance of the SBF formed CaP coat on bone cell response. The surfaces were characterized by Optical Interferometry, Scanning Electron Microscopy (SEM) and X-ray Photoelectron Spectroscopy (XPS). CaP formation was evaluated after 12, 24 and 72 h in simulated body fluid (SBF). Primary human mandibular osteoblast-like cells were cultured on the various surfaces subjected to SBF for 72 h. Cellular attachment, differentiation (osteocalcin) and protein production (TGF-beta(1)) was evaluated after 3 h and 10 days respectively. Despite different morphological appearances, the roughness of the differently modified surfaces was similar. The possibly bioactive surfaces gave rise to an earlier CaP formation than the blasted surface, however, after 72 h the blasted surface demonstrated increased CaP formation compared to the possibly bioactive surfaces. Subsequent bone cell attachment was correlated to neither surface roughness nor the amount of formed CaP after SBF treatment. In contrast, osteocalcin and TGF-beta(1) production were largely correlated to the amount of CaP formed on the surfaces. However, bone response (cell attachment, osteocalcin and TGF-F production) on the blasted controls were similar or increased compared to the SBF treated fluoridated, AH and TiMgO surface.
本研究的目的是比较喷砂处理的和四种不同的可能具有生物活性的商业纯钛表面的钙磷形成(CaP)及随后的骨细胞反应;1. 氟化蚀刻(氟化物),2. 碱热处理(AH),3. 掺入镁离子的阳极氧化(TiMgO),以及4. 纳米羟基磷灰石涂层并热处理(纳米HA),并在体外进行比较。此外,评估模拟体液(SBF)形成的CaP涂层对骨细胞反应的重要性。通过光学干涉测量法、扫描电子显微镜(SEM)和X射线光电子能谱(XPS)对这些表面进行表征。在模拟体液(SBF)中培养12、24和72小时后评估CaP的形成。将原代人下颌骨成骨样细胞培养在经过SBF处理72小时的各种表面上。分别在3小时和10天后评估细胞附着、分化(骨钙素)和蛋白质产生(转化生长因子-β1)。尽管形态外观不同,但不同改性表面的粗糙度相似。可能具有生物活性的表面比喷砂处理的表面更早形成CaP,然而,72小时后,喷砂处理的表面与可能具有生物活性的表面相比,CaP形成增加。随后的骨细胞附着与表面粗糙度和SBF处理后形成的CaP量均无相关性。相反,骨钙素和转化生长因子-β1的产生在很大程度上与表面上形成的CaP量相关。然而,与SBF处理的氟化、AH和TiMgO表面相比,喷砂处理对照组的骨反应(细胞附着、骨钙素和转化生长因子-F产生)相似或增加。