Wang Anyue, Yuan Wenhong, Song Yu, Zang Yanjun, Yu Yanling
Department of Stomatology, School of Stomatology of Qingdao University, Qingdao, China.
Qingdao Municipal Hospital, Qingdao, China.
Front Bioeng Biotechnol. 2022 Feb 23;10:842014. doi: 10.3389/fbioe.2022.842014. eCollection 2022.
To investigate the effect of osseointegration of kaempferol loaded on the surface of micro-nanomorphic implants in ovariectomized rats. Titanium flakes were polished to obtain the PT group, anodized and acid-etched to obtain the NT and WNT groups, loaded with kaempferol to obtain the KNT and KWNT groups, and spin-coated on chitosan-gelatin composite film to obtain the KNT-CG and KWNT-CG groups. experiments were performed to observe the physicochemical properties of the titanium tablets in each group through scanning electron microscopy and contact angle experiments. The cytotoxicity and drug release pattern were observed using CCK-8 and drug release assays. An osteoporosis rat model was established. Pure titanium implants were divided into PT, NT, WNT, KNT-CG, and KWNT-CG groups after the same treatment and used in the experiments and then implanted in the femur of mice in each group. After 4 weeks, all samples were collected for toluidine blue staining, micro-computed tomography scanning, and bone morphometry analysis to evaluate their osteogenic properties. According to scanning electron microscopy, the surface of the titanium flakes had a micro-nano morphology in the WNT group and the KNT and KWNT groups were functionally loaded with kaempferol. In CCK-8 and drug release experiments, the loaded kaempferol and gelatin composite membranes showed no significant toxic effects on cells. The drug release time in the KNT-CG and KWNT-CG groups was significantly longer than that in the KNT and KWNT groups, with the release time in the KWNT-CG group reaching 15 days. experiments micro-computed tomography and bone morphometry analysis showed that the osteoporosis model had been successfully constructed. The bone volume fraction around the implant increased. Toluidine blue staining showed new bone formation and a significantly increased number of bone trabeculae. Kaempferol micro-nanocomposite coating improved the osseointegration ability of implants in osteoporotic rats.
研究载有山奈酚的微纳形貌植入物在去卵巢大鼠体内的骨整合效果。将钛片抛光得到PT组,进行阳极氧化和酸蚀得到NT组和WNT组,负载山奈酚得到KNT组和KWNT组,旋涂于壳聚糖-明胶复合膜上得到KNT-CG组和KWNT-CG组。通过扫描电子显微镜和接触角实验观察每组钛片的理化性质。使用CCK-8和药物释放试验观察细胞毒性和药物释放模式。建立骨质疏松大鼠模型。经过相同处理后,将纯钛植入物分为PT、NT、WNT、KNT-CG和KWNT-CG组,用于实验,然后植入每组小鼠的股骨中。4周后,收集所有样本进行甲苯胺蓝染色、显微计算机断层扫描和骨形态计量分析,以评估其成骨性能。根据扫描电子显微镜观察,WNT组钛片表面具有微纳形貌,KNT组和KWNT组功能性负载山奈酚。在CCK-8和药物释放实验中,负载山奈酚的明胶复合膜对细胞无明显毒性作用。KNT-CG组和KWNT-CG组的药物释放时间明显长于KNT组和KWNT组,KWNT-CG组的释放时间达到15天。显微计算机断层扫描和骨形态计量分析实验表明骨质疏松模型已成功构建。植入物周围的骨体积分数增加。甲苯胺蓝染色显示有新骨形成,骨小梁数量显著增加。山奈酚微纳复合涂层提高了骨质疏松大鼠植入物的骨整合能力。