Long Yunzi, Huang Guibin, Liu Siyi, Xu Liju, Li Ailing, Qiu Dong, Dong Yanmei
Department of General Dentistry II, Peking University School and Hospital of Stomatology, Beijing 100081, PR China.
Department of Cariology and Endodontology, Peking University School and Hospital of Stomatology, Beijing 100081, PR China.
Regen Biomater. 2024 Sep 26;11:rbae114. doi: 10.1093/rb/rbae114. eCollection 2024.
A light-cured bioactive composite, TheraCal LC, is easy to handle and fast-setting. But poor water absorption restricted its bioactivity when applied in direct pulp capping (DPC). Enhancing the water absorption of resin-based bioactive materials may be key to optimizing biomineralization procedure of light-cured bioactive materials. We constructed a hygroscopic, light-cured bioactive composite made up of bioactive glass (BG), poly (ethylene glycol) (PEG) and resin in this study. BG was encapsulated into a porogen (i.e. PEG) and mixed into resin matrix. Inductively coupled plasma showed that light-cured BG (LC-BG) exhibited faster ion release and more ion exchange than TheraCal LC did. The formation of macropores and hydroxyapatite crystal coatings on the BG microparticles was observed using scanning electron microscopy. The shear bond strength between the resin and LC-BG group did not significantly differ from the TheraCal LC group. CCK-8 assay showed that the LC-BG extract was nontoxic. Real-time polymerase chain reaction revealed that LC-BG upregulated odontogenic gene expression in human dental pulp cells. DPC assay proved that the LC-BG group exhibited no significant difference in dentin tubule formation ( = 0.659) or odontoblast-like cell layer formation ( = 0.155) from the TheraCal LC group, but exhibited significantly better integrity of the calcified bridge than the TheraCal LC group (=0.039); more DSPP-positive and DMP-1-positive cells were detected in the LC-BG group than in the TheraCal LC group. Although no significant difference in pulpal inflammatory cell infiltration was observed between the LC-BG group and the TheraCal LC group ( = 0.476), fewer interleukin 1β-positive and tumor necrosis factor α-positive cells were detected in the LC-BG group than in the TheraCal LC group. In conclusion, the newly developed hygroscopic LC-BG composite showed better bioactivity and odontogenic differentiation than the TheraCal LC did and induced better integrity of the calcified bridge than the TheraCal LC did .
一种光固化生物活性复合材料TheraCal LC,易于操作且固化速度快。但吸水率低限制了其在直接盖髓术(DPC)中的生物活性。提高树脂基生物活性材料的吸水率可能是优化光固化生物活性材料生物矿化过程的关键。在本研究中,我们构建了一种由生物活性玻璃(BG)、聚乙二醇(PEG)和树脂组成的吸湿光固化生物活性复合材料。BG被包裹在致孔剂(即PEG)中并混入树脂基体。电感耦合等离子体显示,光固化BG(LC-BG)比TheraCal LC表现出更快的离子释放和更多的离子交换。使用扫描电子显微镜观察到BG微粒上大孔和羟基磷灰石晶体涂层的形成。树脂与LC-BG组之间的剪切粘结强度与TheraCal LC组无显著差异。CCK-8检测表明LC-BG提取物无毒。实时聚合酶链反应显示LC-BG上调了人牙髓细胞中牙源性基因的表达。DPC检测证明,LC-BG组与TheraCal LC组在牙本质小管形成(=0.659)或成牙本质细胞样细胞层形成(=0.155)方面无显著差异,但在钙化桥的完整性方面比TheraCal LC组显著更好(=0.039);LC-BG组中检测到的DSPP阳性和DMP-1阳性细胞比TheraCal LC组更多。尽管LC-BG组与TheraCal LC组之间在牙髓炎症细胞浸润方面未观察到显著差异(=0.476),但LC-BG组中检测到的白细胞介素1β阳性和肿瘤坏死因子α阳性细胞比TheraCal LC组更少。总之,新开发的吸湿LC-BG复合材料比TheraCal LC表现出更好的生物活性和牙源性分化,并且在钙化桥的完整性诱导方面比TheraCal LC更好。