Suppr超能文献

锌掺杂介孔生物活性玻璃纳米颗粒对酸蚀冲洗粘结剂微拉伸粘结强度的影响

Effects of Zn-Doped Mesoporous Bioactive Glass Nanoparticles in Etch-and-Rinse Adhesive on the Microtensile Bond Strength.

作者信息

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

机构信息

Department of Orthodontics, Dental Research Institute, Pusan National University, Yangsan 50612, Korea.

School of Materials Science and Engineering, Pusan National University, Busan 46241, Korea.

出版信息

Nanomaterials (Basel). 2020 Sep 29;10(10):1943. doi: 10.3390/nano10101943.

Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/62f2/7601785/db9b8c37f07d/nanomaterials-10-01943-g001.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验