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大鼠颅骨缺损模型中含载药聚合物微粒的胶原膜的成骨评估

Osteogenic evaluation of collagen membrane containing drug-loaded polymeric microparticles in a rat calvarial defect model.

作者信息

Piao Zheng-Gang, Kim Jae-Sung, Son Jun-Sik, Lee Sook-Young, Fang Xian-Hao, Oh Ji-Su, You Jae-Seek, Kim Su-Gwan

机构信息

1 Oral Biology Institute, School of Dentistry, Chosun University , Gwangju, Republic of Korea.

出版信息

Tissue Eng Part A. 2014 Dec;20(23-24):3322-31. doi: 10.1089/ten.TEA.2013.0717.

Abstract

The aim of this study was to develop a functional collagen membrane that is treated with poly (lactic-co-glycolic acid) (PLGA) nanoparticles loaded with dexamethasone (DEX) as a bioactive molecule for guided bone regeneration (GBR). The DEX-loaded PLGA microparticles prepared using water-in-oil standard emulsion method were precoated with positively charged polyethylenimine molecules and later immobilized onto the surface of the collagen membrane; the microparticles were physically immobilized using counter charges of positively charged PLGA microparticles and the negatively charged collagen membrane surface. The release profile of DEX over a 4-week immersion study indicated an initial burst release followed by a sustained release. The performance of this system was investigated using rats with calvarial bone defects. The in vivo evaluation of the defects filled with membrane containing DEX-loaded PLGA microparticles indicated enhanced volume and quality of new bone formation compared with defects that were either unfilled or filled with membrane alone. This innovative platform for bioactive molecule delivery more potently induced osteogenesis, which may be exploited in implantable membranes for stem cell therapy or improved in vivo performance. In conclusion, this newly developed collagen membrane treated with drug-loaded PLGA microparticles might be applicable as a promising bone graft substitute for GBR.

摘要

本研究的目的是开发一种功能性胶原膜,该膜用负载地塞米松(DEX)作为生物活性分子的聚(乳酸-乙醇酸)(PLGA)纳米颗粒处理,用于引导骨再生(GBR)。使用油包水标准乳液法制备的负载DEX的PLGA微粒预先用带正电荷的聚乙烯亚胺分子包被,随后固定在胶原膜表面;微粒通过带正电荷的PLGA微粒和带负电荷的胶原膜表面的相反电荷进行物理固定。在为期4周的浸泡研究中,DEX的释放曲线显示出初始的突释,随后是持续释放。使用具有颅骨缺损的大鼠对该系统的性能进行了研究。对填充有含负载DEX的PLGA微粒的膜的缺损进行的体内评估表明,与未填充或仅填充膜的缺损相比,新骨形成的体积和质量有所增加。这种用于生物活性分子递送的创新平台更有效地诱导了骨生成,这可用于干细胞治疗的可植入膜或改善体内性能。总之,这种新开发的用负载药物的PLGA微粒处理的胶原膜可能作为一种有前景的GBR骨移植替代物。

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