Topical combined application of dexamethasone, vitamin C, and β-sodium glycerophosphate for healing the extraction socket in rabbits

被引:17
作者
Chen, J. [1 ]
He, Y. [1 ]
Shan, C. [2 ]
Pan, Q. [1 ]
Li, M. [1 ]
Xia, D. [1 ]
机构
[1] Hosp Stomatol, Luzhou Med Coll, Dept Oral & Maxillofacial Surg, Orofacial Reconstruct & Regenerat Lab, Luzhou 646000, Peoples R China
[2] Chongqing Med Univ, Yongchuan Hosp, Dept Stomatol, Chongqing, Peoples R China
关键词
tooth extraction socket; osteogenic inducer; gelatin sponge; cone beam computed tomography; BEAM COMPUTED-TOMOGRAPHY; MESENCHYMAL STEM-CELLS; PLATELET-RICH PLASMA; RIDGE PRESERVATION; TOOTH EXTRACTION; ASCORBIC-ACID; ALVEOLAR BONE; IN-VITRO; DIFFERENTIATION; COLLAGEN;
D O I
10.1016/j.ijom.2015.06.011
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
An osteogenic inducer (OI) consisting of dexamethasone, vitamin C, and beta-sodium glycerophosphate has the capacity to induce bone formation in vitro. The aim of this study was to assess the efficacy of the application of this OI on extraction socket healing. The bilateral first mandibular premolars were extracted from 75 New Zealand rabbits. Gelatin sponges carrying OI were implanted into the sockets. Sockets undergoing implantation of gelatin sponges alone were also evaluated, as well as non-implantation sockets. Specimens from each group were evaluated radiographically, histologically, and histomorphometrically using haematoxylin eosin staining. Results showed earlier new bone formation and higher bone quality and quantity in the OI group compared to the other groups, and the differences were significant at 2, 4, 8, and 12 weeks postoperative. The OI significantly reduced the absorption of alveolar bone in terms of height; however, changes in the width were not significantly different between the three groups (P > 0.05). The OI was shown to have a positive effect on healing of the tooth extraction sockets, was inexpensive, and was convenient to use during the operational procedure; therefore this could represent a promising implant material for human clinical application.
引用
收藏
页码:1317 / 1323
页数:7
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