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使用纳米颗粒载体的药物递送系统对多孔磷酸钙颗粒的成骨评估

Osteogenic Evaluation of Porous Calcium Phosphate Granules with Drug Delivery System Using Nanoparticle Carriers.

作者信息

Son Jun Sik, Kwon Tae-yub, Kim Kyo-han

出版信息

J Nanosci Nanotechnol. 2015 Jan;15(1):130-3. doi: 10.1166/jnn.2015.8392.

Abstract

Novel porous biphasic calcium phosphate (BCP) granules incorporated with drug-releasing poly(lactic-co-glycolic acid) (PLGA) nanoparticles were developed as a drug delivery platform for bone regeneration. The charge interaction between the BCP and PLGA nanoparticle surfaces was manipulated to create this combination system. Spherical BCP granules with open micro-channels and PLGA nanoparticles loaded with dexamethasone (DEX) as a model drug were fabricated using a liquid nitrogen method and standard emulsion method, respectively. Polyethyleneimine was coated on the DEX-loaded PLGA nanoparticle surfaces, resulting in a net positively charged surface. Such modified nanoparticles were immobilized physically on the negatively charged BCP granule surfaces. An in vitro evaluation of MG 63 cells cultured for 1 and 2 weeks on the BCP granules containing DEX-loaded PLGA nanoparticles showed greater cell proliferation, differentiation, and a more extensively connected-tissue network than those cultured on the BCP granules alone. This innovative platform for bioactive molecule delivery more potently induced osteogenesis in vitro, which might be exploited in implantable bioceramic bone graft materials for stem cell therapy or improved in vivo performance.

摘要

新型多孔双相磷酸钙(BCP)颗粒与载药聚乳酸-羟基乙酸共聚物(PLGA)纳米颗粒相结合,被开发为一种用于骨再生的药物递送平台。通过控制BCP与PLGA纳米颗粒表面之间的电荷相互作用来构建这种组合系统。分别采用液氮法和标准乳液法制备了具有开放微通道的球形BCP颗粒和负载地塞米松(DEX)作为模型药物的PLGA纳米颗粒。在负载DEX的PLGA纳米颗粒表面包覆聚乙烯亚胺,使其表面带正电荷。这种改性纳米颗粒通过物理方式固定在带负电荷的BCP颗粒表面。对在含有负载DEX的PLGA纳米颗粒的BCP颗粒上培养1周和2周的MG 63细胞进行的体外评估显示,与仅在BCP颗粒上培养的细胞相比,其细胞增殖、分化能力更强,组织网络连接更广泛。这种用于生物活性分子递送的创新平台在体外能更有效地诱导成骨,可用于干细胞治疗的可植入生物陶瓷骨移植材料或改善体内性能。

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