Evaluation of Collagen Membranes Coated with Testosterone and Alendronate to Improve Guided Bone Regeneration in Mandibular Bone Defects in Minipigs.

IF 1 Q3 DENTISTRY, ORAL SURGERY & MEDICINE
eJournal of Oral Maxillofacial Research Pub Date : 2020-11-30 eCollection Date: 2020-07-01 DOI:10.5037/jomr.2020.11304
Bart A J A van Oirschot, John A Jansen, Cindy J J M van de Ven, Edwin J W Geven, Jan A Gossen
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引用次数: 4

Abstract

Objectives: The purpose of the present in vivo study was to evaluate whether pericard collagen membranes coated with ancillary amounts of testosterone and alendronate in a poly-lactic glycolic acid (PLGA) carrier as compared to uncoated membranes will improve early bone regeneration.

Material and methods: In each of 16 minipigs, four standardized mandibular intraosseous defects were made bilaterally. The defects were filled with Bio-Oss® granules and covered with a non-coated or coated membrane. Membranes were spray-coated with 4 layers of PLGA containing testosterone and alendronate resulting in 20, 50 or 125 μg/cm2 of testosterone and 20 µg/cm2 alendronate (F20, F50, F125). Non-coated membranes served as controls (F0). Animals were sacrificed at 6 and 12 weeks after treatment. Qualitative and quantitative histological evaluations of bone regeneration were performed. Differences between groups were assessed by paired Student's t-test.

Results: Light microscopical analysis showed new bone formation that was in close contact with the Bio-Oss® surface without an intervening non-mineralized tissue layer. Histomorphometric analysis of newly formed bone showed a significant 20% increase in area in the F125 coated membrane treated defects (40 [SD 10]%) compared to the F0 treated defects after 6 weeks (33 [SD 10]%, P = 0.013). At week 12, the total percentage of new bone was increased compared to week 6, but no increase in newly formed bone compared to F0 was observed.

Conclusions: The data from this in vivo study indicate that F125 collagen membranes coated with testosterone and alendronate resulted in superior bone formation (+24%) when normalized to control sites using uncoated membranes.

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睾酮和阿仑膦酸包被胶原膜促进小型猪下颌骨缺损引导骨再生的研究。
目的:目前体内研究的目的是评估在聚乳酸乙醇酸(PLGA)载体中包被辅助量的睾酮和阿仑膦酸钠的包皮胶原膜与未包被的膜相比,是否能改善早期骨再生。材料和方法:16头小型猪,每头制造4个标准化的双侧下颌骨骨内缺损。用Bio-Oss®颗粒填充缺陷,并用未涂覆或涂覆的膜覆盖。膜上喷涂4层含睾酮和阿仑膦酸的聚乳酸,睾酮浓度为20、50或125 μg/cm2,阿仑膦酸浓度为20 μg/cm2 (F20、F50、F125)。未涂覆膜作为对照(F0)。动物于治疗后6周和12周处死。进行骨再生的定性和定量组织学评价。组间差异采用配对学生t检验。结果:光镜分析显示新骨形成与Bio-Oss®表面紧密接触,没有中间的非矿化组织层。新形成骨的组织形态学分析显示,6周后,F125涂层膜处理的缺损面积比F0处理的缺损面积增加了20% (40 [SD 10]%) (33 [SD 10]%, P = 0.013)。第12周时,新骨总百分比较第6周有所增加,但新骨未见明显增加。结论:这项体内研究的数据表明,当使用未涂覆的膜将F125胶原膜归一化到对照部位时,睾酮和阿仑膦酸盐包被的F125胶原膜可导致更好的骨形成(+24%)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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