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多功能纳米纤维中空微球促进牙周骨再生。

Multifunctional Nanofibrous Hollow Microspheres for Enhanced Periodontal Bone Regeneration.

机构信息

Department of Biomedical Sciences, Texas A&M University School of Dentistry, Dallas, TX, 75246, USA.

Chemical and Biomedical Engineering Department, University of Missouri, Columbia, MO, 65211, USA.

出版信息

Adv Sci (Weinh). 2024 Jul;11(28):e2402335. doi: 10.1002/advs.202402335. Epub 2024 May 17.

DOI:10.1002/advs.202402335
PMID:38757666
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11267322/
Abstract

Destructive periodontitis destroys alveolar bone and eventually leads to tooth loss. While guided bone regeneration, which is based on creating a physical barrier to hinder the infiltration of epithelial and connective tissues into defect sites, has been widely used for alveolar bone regeneration, its outcomes remain variable. In this work, a multifunctional nanofibrous hollow microsphere (NFHMS) is developed for enhanced alveolar bone regeneration. The NFHMS is first prepared via combining a double emulsification and a thermally induced phase separation process. Next, E7, a short peptide with high specific affinity to bone marrow-derived stem cells (BMSCs), is conjugated onto the surface of NFHMS. After that, bone forming peptide (BFP), a short peptide derived from bone morphology protein 7 is loaded in calcium phosphate (CaP) nanoparticles, which are further encapsulated in the hollow space of the NFHMS-E7 to form NFHMS-E7-CaP/BFP. The NFHMS-E7-CaP/BFP selectively promoted the adhesion of BMSCs and expelled the adhesion of fibroblasts and epithelial cells. In addition, the BFP is sustainedly released from the NFHMS-E7-CaP/BFP to enhance the osteogenesis of BMSCs. A rat challenging fenestration defect model showed that the NFHMS-E7-CaP/BFP significantly enhanced alveolar bone tissue regeneration. This work provides a novel bioengineering approach for guided bone regeneration.

摘要

破坏性牙周炎会破坏牙槽骨,最终导致牙齿脱落。引导骨再生术基于创建物理屏障以阻止上皮和结缔组织渗透到缺损部位,已被广泛用于牙槽骨再生,但效果仍存在差异。在这项工作中,开发了一种多功能纳米纤维中空微球(NFHMS)以增强牙槽骨再生。NFHMS 首先通过双重乳化和热致相分离工艺制备。然后,将具有高骨髓源性干细胞(BMSCs)特异性亲和力的短肽 E7 接枝到 NFHMS 表面。接下来,将骨形成肽(BFP),一种源自骨形态发生蛋白 7 的短肽载入到磷酸钙(CaP)纳米颗粒中,然后将其进一步封装在 NFHMS-E7 的中空空间中,形成 NFHMS-E7-CaP/BFP。NFHMS-E7-CaP/BFP 选择性促进 BMSCs 的黏附,并排斥成纤维细胞和上皮细胞的黏附。此外,BFP 从 NFHMS-E7-CaP/BFP 中持续释放,以增强 BMSCs 的成骨作用。大鼠挑战开窗缺损模型表明,NFHMS-E7-CaP/BFP 可显著增强牙槽骨组织再生。这项工作为引导骨再生提供了一种新的生物工程方法。

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