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通过海绵状单分散 PLGA/纳米-MgO-海藻酸钠核壳微球装置精确控制镁离子的释放,以实现原位骨再生。

Precisely controlled delivery of magnesium ions thru sponge-like monodisperse PLGA/nano-MgO-alginate core-shell microsphere device to enable in-situ bone regeneration.

机构信息

Department of Orthopaedics and Traumatology, The University of Hong Kong, Hong Kong, China; Shenzhen Key Laboratory for Innovative Technology in Orthopaedic Trauma, The University of Hong Kong Shenzhen Hospital, 1 Haiyuan 1st Road, Futian District, Shenzhen, China.

Shenzhen Key Laboratory for Innovative Technology in Orthopaedic Trauma, The University of Hong Kong Shenzhen Hospital, 1 Haiyuan 1st Road, Futian District, Shenzhen, China.

出版信息

Biomaterials. 2018 Aug;174:1-16. doi: 10.1016/j.biomaterials.2018.05.011. Epub 2018 May 8.

Abstract

A range of magnesium ions (Mg) used has demonstrated osteogenic tendency in vitro. Hence, we propose to actualize this concept by designing a new system to precisely control the Mg delivery at a particular concentration in vivo in order to effectively stimulate in-situ bone regeneration. To achieve this objective, a monodisperse core-shell microsphere delivery system comprising of poly (lactic-co-glycolic acid) (PLGA) biopolymer, alginate hydrogel, and magnesium oxide nano-particles has been designed by using customized microfluidic capillary device. The PLGA-MgO sponge-like spherical core works as a reservoir of Mg while the alginate shell serves as physical barrier to control the outflow of Mg at ∼50 ppm accurately for 2 weeks via its adjustable surface micro-porous network. With the aid of controlled release of Mg, the new core-shell microsphere system can effectively enhance osteoblastic activity in vitro and stimulate in-situ bone regeneration in vivo in terms of total bone volume, bone mineral density (BMD), and trabecular thickness after operation. Interestingly, the Young's moduli of formed bone on the core-shell microsphere group have been restored to ∼96% of that of the surrounding matured bone. These findings indicate that the concept of precisely controlled release of Mg may potentially apply for in-situ bone regeneration clinically.

摘要

一系列的镁离子(Mg)已被证明具有体外成骨倾向。因此,我们拟通过设计一个新的系统来实现这一概念,该系统能够在体内以特定浓度精确控制镁的释放,从而有效地刺激原位骨再生。为了实现这一目标,我们使用定制的微流控毛细管装置设计了一种由聚(乳酸-共-乙醇酸)(PLGA)生物聚合物、藻酸盐水凝胶和氧化镁纳米粒子组成的单分散核壳微球递送系统。PLGA-MgO 海绵状球形核作为镁的储库,而藻酸盐壳作为物理屏障,通过其可调节的表面微孔网络,可将镁的释放精确控制在约 50ppm,持续 2 周。通过镁的控制释放,新的核壳微球系统能够有效增强体外成骨细胞的活性,并在术后从总骨量、骨密度(BMD)和小梁厚度等方面刺激体内原位骨再生。有趣的是,核壳微球组形成的骨的杨氏模量已恢复到周围成熟骨的约 96%。这些发现表明,精确控制镁释放的概念可能有潜力应用于临床原位骨再生。

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