Department of Prosthodontics, Faculty of Odontology, Malmö University, 205 06, Malmö, Sweden.
Department of Chemistry and Chemical Engineering, Applied Chemistry, Chalmers University of Technology, 412 96, Gothenburg, Sweden.
J Biomed Mater Res B Appl Biomater. 2017 Oct;105(7):2118-2125. doi: 10.1002/jbm.b.33752. Epub 2016 Jul 13.
The release of magnesium ions (Mg ) from titanium surfaces has been shown to boost the initial biological response of peri-implant bone and to increase the biomechanical strength of osseointegration. The objective of the present paper was to investigate if the initial improvement in osseointegration would influence the bone remodeling also during the maturation stage of bone healing.
Titanium implants were coated with mesoporous titania layers and either loaded with Mg (test group) or left untreated (control group). The implants were inserted in the tibiae of 10 New Zealand White rabbits. Osseointegration was assessed after 6 weeks by means of biomechanical testing (RTQ), non-decalcified histology and histomorphometry (BIC%, BA%, NBA%). The expression of genes involved in the bone formation and remodeling was quantified using qPCR.
Mg releasing mesoporous titania coatings showed, on average, higher removal torques and histomorphometrical outcomes (RTQ: 17.2 Ncm vs. 15 Ncm; BIC: 38.8% vs. 32.1%; BA%: 71.6% vs. 64%; NBA% 62.5% vs. 54% for the tests vs the controls); however, the differences were not statistically significant. Three osteogenic markers, osteocalcin (OC), collagen 1 alpha 1 (COL1A1), and alkalin phosphatase (ALPL), were respectively 2-fold, 1.53-fold, and 1.13-fold up-regulated in the control group compared to the test. The expression of COL1A1 was particularly high in both groups, while the biomarkers for remodeling and inflammation showed a low expression in both groups.
The results suggested that the initial enhancement in osseointegration induced by magnesium release from mesoporous titania coatings has no detrimental effects during bone maturation. © 2016 Wiley Periodicals, Inc. J Biomed Mater Res Part B: Appl Biomater, 105B: 2118-2125, 2017.
从钛表面释放镁离子(Mg)已被证明可以增强植入骨的初始生物学反应,并提高骨整合的生物力学强度。本研究的目的是探讨初始骨整合的改善是否会影响骨愈合成熟阶段的骨重塑。
用介孔二氧化钛层涂覆钛植入物,并对其进行镁(实验组)或不处理(对照组)加载。将植入物插入 10 只新西兰白兔的胫骨中。通过生物力学测试(RTQ)、非脱钙组织学和组织形态计量学(BIC%、BA%、NBA%)在 6 周后评估骨整合。使用 qPCR 定量分析参与骨形成和重塑的基因表达。
释放镁的介孔二氧化钛涂层的平均去除扭矩和组织形态计量学结果较高(RTQ:17.2 Ncm 与 15 Ncm;BIC:38.8%与 32.1%;BA%:71.6%与 64%;NBA%:62.5%与 54%,实验组与对照组);然而,差异无统计学意义。与实验组相比,对照组的成骨标志物骨钙素(OC)、胶原 1 阿尔法 1(COL1A1)和碱性磷酸酶(ALPL)分别上调 2 倍、1.53 倍和 1.13 倍。COL1A1 在两组中的表达均较高,而重塑和炎症的生物标志物在两组中的表达均较低。
结果表明,介孔二氧化钛涂层中镁释放引起的初始骨整合增强在骨成熟过程中没有不良影响。©2016 Wiley 期刊,Inc. J 生物医学材料研究部分 B:应用生物材料,105B:2118-2125,2017。