Polydioxanone Enhances Bone Regeneration After Resection and Reconstruction of Rat Femur with rhBMP2.

IF 2.7 4区 医学 Q3 CELL & TISSUE ENGINEERING Tissue engineering. Part C, Methods Pub Date : 2024-03-01 Epub Date: 2024-01-25 DOI:10.1089/ten.tec.2023.0304
Barbara Ribeiro Rios, Stéfany Barbosa, William Phillip Pereira da Silva, Mario Jefferson Quirino Louzada, Edilson Ervolino, Eduardo C Kalil, Jamil Awad Shibli, Leonardo P Faverani
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Abstract

The aim of this study was to assess the bone regeneration potential of a polydioxanone (PDO) scaffold together with recombinant human bone morphogenetic protein-2 (rhBMP-2) for the reconstruction of large bone defect. In total, 24 male rats (6 months old) were subjected to bilateral femoral stabilization using titanium plates to create a 2 mm gap, and reconstruction using rhBMP-2 (Infuse®; 3.25 μg). The bone defects were covered with PDO (PDO group), or with titanium mesh (Ti group). Animals were euthanized on days 14 and 60. Simultaneously, 16 rats received PDO and Ti in their dorsum for the purpose of biocompatibility analysis at 3, 5, 7, and 10 days postoperatively. X-ray densitometry showed a higher density in the PDO group on day 14. On day 60, coverage of the bone defect with PDO showed a larger quantity of newly formed bone than that found for the Ti group, a lower inflammatory infiltrate value, and a more significant number of blood vessels on day 14. By immunohistochemical assessment, runt-related transcription factor 2 (RUNX2) and osteocalcin (OCN) showed higher labeling on day 14 in the PDO group. On day 60, bone morphogenetic protein-2 (BMP-2) showed higher labeling in the PDO group, whereas Ti showed higher labeling for osteoprotegerin, nuclear factor kappa B ligand-activating receptor, RUNX2, and OCN. Furthermore, biocompatibility analysis showed a higher inflammatory response in the Ti group. The PDO scaffold enhanced bone regeneration when associated with rhBMP-2 in rat femur reconstruction. Impact statement Regeneration of segmental bone defects is a difficult task, and several techniques and materials have been used. Recent advances in the production of synthetic polymers, such as polydioxanone (PDO), produced by three-dimensional printing, have shown distinct characteristics that could improve tissue regeneration even in an important bone defect. The present preclinical study showed that PDO membranes used as scaffolds to carry recombinant human bone morphogenetic protein-2 (rhBMP-2) improved bone tissue regeneration by more than 8-fold when compared with titanium mesh, suggesting that PDO membranes could be a feasible and useful material for use in guided bone regeneration. (In English, viable is only used for living creatures capable of sustaining life.

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聚二氧杂蒽酮能增强大鼠股骨切除和使用 rhBMP2 重建后的骨再生。
本研究旨在评估聚二氧杂蒽酮(PDO)支架与重组人骨形态发生蛋白-2(rhBMP-2)在重建大面积骨缺损中的骨再生潜力。共对 24 只雄性大鼠(6 个月大)进行了双侧股骨稳定手术,使用钛板造成 2 毫米的间隙,并使用 rhBMP-2 (Infuse®;3.25 μg)进行重建。骨缺损用 PDO(PDO 组)或钛网(Ti 组)覆盖。动物在第 14 天和第 60 天安乐死。同时,16 只大鼠的背部接受了 PDO 和钛网,以便在术后 3、5、7 和 10 天进行生物相容性分析。X 射线密度测量显示,第 14 天时,PDO 组的密度更高。第 60 天,PDO 覆盖骨缺损的情况显示,与钛组相比,新形成的骨量更多,炎症浸润值更低,第 14 天的血管数量更多。通过免疫组化评估,PDO 组在第 14 天显示出更高的润相关转录因子 2(RUNX2)和骨钙素(OCN)标记。在第 60 天,PDO 组的骨形态发生蛋白-2(BMP-2)标记较高,而 Ti 组的骨保护素、核因子卡巴 B 配体激活受体、RUNX2 和 OCN 标记较高。此外,生物相容性分析表明,Ti 组的炎症反应更高。在大鼠股骨重建中,当与 rhBMP-2 结合使用时,PDO 支架可促进骨再生。
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来源期刊
Tissue engineering. Part C, Methods
Tissue engineering. Part C, Methods Medicine-Medicine (miscellaneous)
CiteScore
5.10
自引率
3.30%
发文量
136
期刊介绍: Tissue Engineering is the preeminent, biomedical journal advancing the field with cutting-edge research and applications that repair or regenerate portions or whole tissues. This multidisciplinary journal brings together the principles of engineering and life sciences in the creation of artificial tissues and regenerative medicine. Tissue Engineering is divided into three parts, providing a central forum for groundbreaking scientific research and developments of clinical applications from leading experts in the field that will enable the functional replacement of tissues. Tissue Engineering Methods (Part C) presents innovative tools and assays in scaffold development, stem cells and biologically active molecules to advance the field and to support clinical translation. Part C publishes monthly.
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