Chen Fa-ming, Ma Zhi-wei, Dong Guang-ying, Wu Zhi-fen
Department of Periodontology and Oral Medicine, School of Stomatology, Fourth Military Medical University, Xi'an, China.
Acta Pharmacol Sin. 2009 Apr;30(4):485-93. doi: 10.1038/aps.2009.15. Epub 2009 Mar 23.
Localized delivery of growth factors has significant potential as a future therapeutic strategy in tissue engineering and regenerative medicine. A nanoparticle vehicle was created and evaluated in this study with the intent to deliver growth factors for periodontal regeneration.
Novel composite nanoparticles based on glycidyl methacrylate derivatized dextrans (Dex-GMA) and gelatin were fabricated by a facile method without using any organic solvents. The configurations of the resultant nanoparticles were evaluated by transmission electron microscopy, scanning electron microscopy, and atomic force microscope. Their surfaces were characterized by zeta-potential measurements, after which their properties including swelling, degradation, drug release, and cytotoxicity were also investigated using in vitro models.
The particle size of Dex-GMA/gelatin nanoparticles (DG-NPs) ranged from 20 to 100 nm and showed a mono-disperse size distribution (mean diameter 53.7 nm) and a strongly negative surface zeta potential (-20 mV). The DG-NPs were characterized by good swelling and degradation properties in media including dextranase. The in vitro drug release studies showed that the efficient bone morphogenetic protein (BMP) release from DG-NPs was maintained for more than 12 d under degradation conditions, where more than 90% of the loaded BMP was released. No any relevant cell damage caused by DG-NPs was found in the cytotoxicity tests for a period of 24 h.
These combined results demonstrate that DG-NPs fulfill the basic prerequisites for growth factor delivery. With further in vivo studies, those nanoparticles may offer a promising vehicle for the delivery of active drugs to the periodontium.
生长因子的局部递送作为组织工程和再生医学未来的治疗策略具有巨大潜力。本研究制备并评估了一种纳米颗粒载体,旨在递送生长因子用于牙周组织再生。
基于甲基丙烯酸缩水甘油酯衍生化葡聚糖(Dex-GMA)和明胶制备新型复合纳米颗粒,采用简便方法,无需使用任何有机溶剂。通过透射电子显微镜、扫描电子显微镜和原子力显微镜评估所得纳米颗粒的形态。通过zeta电位测量对其表面进行表征,之后还使用体外模型研究了它们的性质,包括溶胀、降解、药物释放和细胞毒性。
Dex-GMA/明胶纳米颗粒(DG-NPs)的粒径范围为20至100 nm,呈现单分散粒径分布(平均直径53.7 nm)以及强烈的负表面zeta电位(-20 mV)。DG-NPs在包括葡聚糖酶的培养基中具有良好的溶胀和降解性能。体外药物释放研究表明,在降解条件下,DG-NPs能有效释放骨形态发生蛋白(BMP)超过12天,其中超过90%的负载BMP被释放。在24小时的细胞毒性试验中未发现DG-NPs引起任何相关细胞损伤。
这些综合结果表明DG-NPs满足生长因子递送的基本前提条件。随着进一步的体内研究,这些纳米颗粒可能为向牙周组织递送活性药物提供一种有前景的载体。