Sultan Nessma, Camilleri Josette, Scheven Ben A
Department of Oral Biology, Faculty of Dentistry, Mansoura University, Mansoura, Egypt.
Oral Biology and Dental Morphology, Faculty of Dentistry, Mansoura National University, Gamasa, 7731168, Egypt.
Odontology. 2025 Apr;113(2):585-597. doi: 10.1007/s10266-024-00994-2. Epub 2024 Sep 14.
Regeneration of dentin and preserving pulp vitality are essential targets for vital pulp therapy. Our study aimed to evaluate a novel biomimetic pulp capping agent with increased dentin regenerative activities. To produce demineralised dentin matrix (DDM) particles, human extracted teeth were ground and treated with ethylene diamine tetra-acetic acid solution. DDM particles were added to sodium alginate and this combination was dripped into a 5% calcium chloride to obtain DDM hydrogel (DDMH). The eluants of both DDMH and mineral trioxide aggregate (MTA) were tested using an MTT assay to detect their cytotoxic effect on dental pulp stem cells (DPSC). Collagen-I (COL-I) gene expression was analysed on DPSC exposed to different dilutions of pulp capping material eluants by real-time quantitative polymerase chain reaction. Acridine orange staining was used to monitor the cell growth over the tested materials. Agar diffusion assay was utilised to test the antibacterial effect of DDMH and MTA compared to controls. MTT assay revealed that neat eluates of DDMH promoted DPSC viability. However, neat eluates of MTA were cytotoxic on DPSC after 72 h of culture. Moreover, DPSC were capable of growth and attached to the surface of DDMH, while they showed a marked reduction in their number when cultured on the MTA surface for one week, as shown by the acridine orange stain. In DPSC cultured with DDMH eluates, the COL-I gene was overexpressed compared to those cultured with MTA eluants. DDMH had significant antimicrobial activity in comparison to MTA after 24 h incubation. This in vitro study showed that DDMH could be an alternative pulp capping agent for regenerative endodontics.
牙本质再生和保持牙髓活力是牙髓治疗的重要目标。我们的研究旨在评估一种具有增强牙本质再生活性的新型仿生牙髓盖髓剂。为制备脱矿牙本质基质(DDM)颗粒,将人拔除的牙齿研磨并用乙二胺四乙酸溶液处理。将DDM颗粒添加到海藻酸钠中,然后将此混合物滴入5%的氯化钙溶液中以获得DDM水凝胶(DDMH)。使用MTT法检测DDMH和三氧化矿物凝聚体(MTA)的洗脱液对牙髓干细胞(DPSC)的细胞毒性作用。通过实时定量聚合酶链反应分析暴露于不同稀释度牙髓盖髓材料洗脱液的DPSC上的I型胶原(COL-I)基因表达。使用吖啶橙染色监测受试材料上的细胞生长情况。利用琼脂扩散试验检测DDMH和MTA与对照相比的抗菌效果。MTT试验显示,DDMH的纯洗脱液可促进DPSC的活力。然而,培养72小时后,MTA的纯洗脱液对DPSC具有细胞毒性。此外,DPSC能够生长并附着于DDMH表面,而如吖啶橙染色所示,当在MTA表面培养一周时,其数量显著减少。与用MTA洗脱液培养的DPSC相比,用DDMH洗脱液培养的DPSC中COL-I基因过度表达。孵育24小时后,与MTA相比,DDMH具有显著的抗菌活性。这项体外研究表明,DDMH可能是再生牙髓治疗的一种替代牙髓盖髓剂。