Choi Yeonju, Sun Woogyeong, Kim Yeon, Kim In-Ryoung, Gong Mi-Kyung, Yoon Seog-Young, Bae Moon-Kyoung, Park Bong-Soo, Park Soo-Byung, Kim Yong-Il
Department of Orthodontics, Dental Research Institute, Pusan National University, Yangsan 50612, Korea.
School of Materials Science and Engineering, Pusan National University, Busan 46241, Korea.
Nanomaterials (Basel). 2020 Sep 29;10(10):1943. doi: 10.3390/nano10101943.
The purpose of this study was to assess the effects in the dentin bond strength of dental adhesives (DAs) and biological effects using zinc (Zn)-doped mesoporous bioactive glass nanoparticles (MBN-Zn). Synthesized MBN and MBN-Zn were characterized by scanning electron microscopy (SEM), X-ray diffraction and the Brunauer, Emmett and Teller (BET) method. The matrix metalloproteinases (MMP) inhibition effects of DA-MBN and DA-MBN-Zn were analyzed. The microtensile bond strength (MTBS) test was conducted before and after thermocycling to investigate the effects of MBN and MBN-Zn on the MTBS of DAs. The biological properties of DA-MBN and DA-MBN-Zn were analyzed with human dental pulp stem cells (hDPSCs). Compared with the DA, only the DA-1.0% MBN and DA-1.0% MBN-Zn exhibited a statistically significant decrease in MMP activity. The MTBS values after thermocycling were significantly increased in DA-1.0% MBN and DA-1.0% MBN-Zn compared with the DA ( < 0.05). It was confirmed via the MTT assay that there was no cytotoxicity for hDPSCs at 50% extract. In addition, significant increases in the alkaline phosphatase activity and Alizarin Red S staining were observed only in DA-1.0%MBN-Zn. These data suggest the 1.0% MBN and 1.0% MBN-Zn enhance the remineralization capability of DAs and stabilize the long-term MTBS of DAs by inhibiting MMPs.
本研究的目的是评估使用锌(Zn)掺杂的介孔生物活性玻璃纳米颗粒(MBN-Zn)对牙科粘合剂(DAs)牙本质粘结强度的影响以及生物学效应。通过扫描电子显微镜(SEM)、X射线衍射和布鲁诺尔-埃米特-泰勒(BET)方法对合成的MBN和MBN-Zn进行了表征。分析了DA-MBN和DA-MBN-Zn对基质金属蛋白酶(MMP)的抑制作用。在热循环前后进行微拉伸粘结强度(MTBS)测试,以研究MBN和MBN-Zn对DAs的MTBS的影响。用人牙髓干细胞(hDPSCs)分析了DA-MBN和DA-MBN-Zn的生物学特性。与DA相比,只有DA-1.0% MBN和DA-1.0% MBN-Zn的MMP活性有统计学意义的降低。与DA相比,DA-1.0% MBN和DA-1.0% MBN-Zn热循环后的MTBS值显著增加(<0.05)。通过MTT试验证实,50%提取物对hDPSCs没有细胞毒性。此外,仅在DA-1.0%MBN-Zn中观察到碱性磷酸酶活性和茜素红S染色显著增加。这些数据表明,1.0% MBN和1.0% MBN-Zn通过抑制MMPs增强了DAs的再矿化能力,并稳定了DAs的长期MTBS。