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载克林霉素磷酸酯和骨形态发生蛋白 7 的联合纳米粒-接枝和纳米粒-膜制剂用于牙槽骨再生的体外和体内评价。

Clindamycin phosphate and bone morphogenetic protein-7 loaded combined nanoparticle-graft and nanoparticle-film formulations for alveolar bone regeneration - An in vitro and in vivo evaluation.

机构信息

Ankara University, Faculty of Pharmacy, Department of Pharmaceutical Technology, 06560 Ankara, Türkiye; Duzce University, Faculty of Pharmacy, Department of Pharmaceutical Technology, 81620 Duzce, Türkiye.

Ankara University, Faculty of Pharmacy, Department of Pharmaceutical Technology, 06560 Ankara, Türkiye.

出版信息

Int J Pharm. 2023 Apr 5;636:122826. doi: 10.1016/j.ijpharm.2023.122826. Epub 2023 Mar 12.

DOI:10.1016/j.ijpharm.2023.122826
PMID:36918117
Abstract

Commonly utilized techniques for healing alveolar bone destruction such as the use of growth factors, suffering from short half-life, application difficulties, and the ability to achieve bioactivity only in the presence of high doses of growth factor. The sustained release of growth factors through a scaffold-based delivery system offers a promising and innovative tool in dentistry. Furthermore, it is suggested to guide the host response by using antimicrobials together with growth factors to prevent recovery and achieve ideal regeneration. Herein, the aim was to prepare and an in vitro - in vivo evaluation of bone morphogenetic protein 7 (BMP-7) and clindamycin phosphate (CDP) loaded polymeric nanoparticles, and their loading into the alginate-chitosan polyelectrolyte complex film or alloplastic graft to accelerate hard tissue regeneration. PLGA nanoparticles containing CDP and BMP-7, separately or together, were prepared using the double emulsion solvent evaporation technique. Through in vitro assays, it was revealed that spherical particles were homogeneously distributed in the combination formulations, and sustained release could be achieved for >12 weeks with all formulations. Also, results from the micro-CT and histopathological analyses indicated that CDP and BMP-7 loaded nanoparticle-film formulations were more effective in treatment than the nanoparticle loaded grafts.

摘要

常用于修复牙槽骨破坏的方法,如生长因子的应用,存在半衰期短、应用困难以及只有在高剂量生长因子存在的情况下才能实现生物活性等问题。通过支架递送系统持续释放生长因子为牙科提供了一种有前途和创新的工具。此外,有人建议使用抗生素与生长因子一起引导宿主反应,以防止恢复并实现理想的再生。本文旨在制备并进行骨形态发生蛋白 7(BMP-7)和克林霉素磷酸(CDP)负载的聚合物纳米粒子的体外-体内评价,并将其载入藻酸盐-壳聚糖聚电解质复合膜或同种异体移植物中以加速硬组织再生。分别或联合使用 PLGA 纳米粒子,通过双乳液溶剂蒸发技术制备 CDP 和 BMP-7。通过体外实验表明,在组合配方中均匀分布着球形颗粒,所有配方都可以实现 >12 周的持续释放。此外,微 CT 和组织病理学分析的结果表明,载有 CDP 和 BMP-7 的纳米粒子-薄膜配方在治疗方面比载有纳米粒子的移植物更有效。

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