盐酸米诺环素作为一种潜在的佐剂,在骨外骨增强模型中改善骨代用品的骨传导和骨诱导性能:在大鼠中的初步观察

Bob Biewer, Dorien van Hede, E. Rompen, M. Mittelbronn, P. Quatresooz, F. K. Borgmann
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摘要

摘要目的本研究旨在确定盐酸米诺环素在引导骨增强模型中作为新骨生成填充材料时,是否会影响脱蛋白牛骨矿物质(DBBM)和生物活性玻璃(BG)颗粒的行为。材料与方法在大鼠颅骨上放置2个封闭的钛帽。一个充满BG颗粒,第二个充满DBBM颗粒,两者之前都与血液混合(对照组)。在二甲胺四环素HCl负载组(实验),移植物另外放置在二甲胺四环素溶液中。4周、8周和16周后采集样本。一半样品包埋在甲基丙烯酸甲酯中进行未钙化组织学分析,另一半样品固定,脱钙,包埋在石蜡中进行经典组织学分析。结果对照组在DBBM切片中突出了与BG颗粒相关的骨传导和骨诱导反应,以及骨传导反应。在BG颗粒中加入盐酸米诺环素对结果没有可测量的影响。在米诺环素HCl负载的DBBM切片;然而,在8周和16周后,可以观察到自发骨化的区域。结论:我们的观察结果表明,在本研究设计的限制下,米诺环素HCl可能会增加DBBM的一些骨诱导特性。需要进一步的调查来完善目前的结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Minocycline Hydrochloride as a Potential Adjuvant to Improve Osteoconductive and Osteoinductive Properties of Bone Substitutes in an Extra-Skeletal Bone Augmentation Model: Preliminary Observations in Rats
Abstract Objectives The present study was performed to determine if minocycline HCl could influence the behavior of deproteinized bovine bone mineral (DBBM) and bioactive glass (BG) particles when used as filler material for new bone generation in a guided bone augmentation model. Materials and Methods Two occlusive titanium caps were placed on the rat calvaria. One filled with BG particles, the second with DBBM particles, both previously mixed with blood (control). In minocycline HCl loaded groups (experimental), grafts were additionally placed into a minocycline solution. Samples were harvested after 4, 8, and 16 weeks. Half of the samples were embedded in methylmethacrylate for undecalcified histology and the other half was fixed, decalcified, and embedded in paraffin for classical histologic analysis. Results The control groups highlighted osteoconductive and osteoinductive responses associated to BG particles, as well as an osteoconductive reaction, in DBBM sections. The addition of minocycline HCl to BG particles had no measurable influence on the result. In minocycline HCl loaded DBBM sections; however, areas of spontaneous ossification could be observed after 8 and 16 weeks. Conclusion Our observations suggest that minocycline HCl may add some osteoinductive properties to DBBM within the limitations of this study design. Further investigations are needed to refine the present results.
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