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[镁掺杂纳米多孔钛涂层的生物学特性及成骨分化]

[Biological characteristics and osteogenic differentiation of magnesium-doped nanoporous titanium coating].

作者信息

Zhao Shan, Zhang Lin, Li Sheng-Nan, Kang Nan, Meng Jian, Li Xiao-Dong

机构信息

Department of Stomatology, Central Hospital of Xuzhou. Xuzhou 221000, Jiangsu Province, China. E-mail:

出版信息

Shanghai Kou Qiang Yi Xue. 2024 Feb;33(1):6-12.

Abstract

PURPOSE

Bioactive magnesium ions were successfully incorporated into the nanoporous titanium base coating by micro-arc oxidation(MAO), and its physical properties and osteogenic effects were explored.

METHODS

Non-magnesium-containing and magnesium-containing titanium porous titanium coatings(MAO, MAO-mg) were prepared by changing the composition of MAO electrolyte and controlling the doping of magnesium in porous titanium coatings. The samples were characterized by scanning electron microscope (SEM), roughness, contact angle and energy dispersive X-ray spectrometer (EDS). Mg release ability of magnesium-doped nanoporous titanium coatings was determined by inductively coupled plasma/optical emission spectrometer(ICP-OES). The structure of the cytoskeleton was determined by live/dead double staining, CCK-8 detection of material proliferation-toxicity, and staining of β-actin using FITC-phalloidin. The effects of the coating on osteogenic differentiation in vitro were determined by alizarin red (ARS), alkaline phosphatase (ALP) staining and real-time polymerase chain reaction (qRT-PCR). SPSS 25.0 software package was used for statistical analysis.

RESULTS

The MAO electrolyte with magnesium ions did not change the surface characteristics of the porous titanium coating. Each group prepared by MAO had similar microporous structure(P>0.05). There was no significant difference in surface roughness and contact angle between MAO treatment group (MAO, MAO-mg)(P>0.05), but significantly higher than that of Ti group (P<0.05). With the passage of cell culture time, MAO-mg group promoted cell proliferation (P<0.05). MAO-mg group was significantly higher than other groups in ALP and ARS staining. The expression of Runx2 mRNA (P<0.05), ALP(P<0.05) and osteocalcin OCN(P<0.05) in MAO-mg group was significantly higher than that in Ti and MAO groups.

CONCLUSIONS

MAO successfully prepared magnesium-containing nanoporous titanium coating, and showed a significant role in promoting osteogenic differentiation.

摘要

目的

通过微弧氧化(MAO)将生物活性镁离子成功引入纳米多孔钛基涂层,并探究其物理性能和成骨效果。

方法

通过改变MAO电解液的成分并控制镁在多孔钛涂层中的掺杂量,制备不含镁和含镁的钛多孔钛涂层(MAO、MAO-mg)。采用扫描电子显微镜(SEM)、粗糙度、接触角和能量色散X射线光谱仪(EDS)对样品进行表征。用感应耦合等离子体/光发射光谱仪(ICP-OES)测定掺镁纳米多孔钛涂层的镁释放能力。通过活/死双染色、CCK-8检测材料增殖毒性以及使用FITC-鬼笔环肽对β-肌动蛋白进行染色来确定细胞骨架的结构。通过茜素红(ARS)、碱性磷酸酶(ALP)染色和实时聚合酶链反应(qRT-PCR)来确定涂层对体外成骨分化的影响。使用SPSS 25.0软件包进行统计分析。

结果

含镁离子的MAO电解液未改变多孔钛涂层的表面特性。MAO制备的各组具有相似的微孔结构(P>0.05)。MAO处理组(MAO、MAO-mg)之间的表面粗糙度和接触角无显著差异(P>0.05),但显著高于钛组(P<0.05)。随着细胞培养时间的推移,MAO-mg组促进细胞增殖(P<0.05)。MAO-mg组在ALP和ARS染色方面显著高于其他组。MAO-mg组中Runx2 mRNA(P<0.05)、ALP(P<0.05)和骨钙素OCN(P<0.05)的表达显著高于钛组和MAO组。

结论

MAO成功制备了含镁纳米多孔钛涂层,并在促进成骨分化方面发挥了显著作用。

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