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新型聚(L-乳酸)/纳米羟基磷灰石/阿仑膦酸钠载壳聚糖微球杂化支架修复大段骨缺损:体外与体内研究。

Reconstruction of Large-scale Defects with a Novel Hybrid Scaffold Made from Poly(L-lactic acid)/Nanohydroxyapatite/Alendronate-loaded Chitosan Microsphere: in vitro and in vivo Studies.

机构信息

Department of Orthopedics, Hunan Cancer Hospital and The Affiliated Cancer Hospital of Xiangya School of Medicine, Central South University, Changsha, 410013, Hunan, China.

Department of Orthopedics, Xiangya Hospital, Central South University, Changsha, 410011, China.

出版信息

Sci Rep. 2017 Mar 23;7(1):359. doi: 10.1038/s41598-017-00506-z.

Abstract

A chitosan-based microsphere delivery system has been fabricated for controlled release of alendronate (AL). The present study aimed to incorporate the chitosan/hydroxyapatite microspheres-loaded with AL (CH/nHA-AL) into poly(L-lactic acid)/nanohydroxyapatite (PLLA/nHA) matrix to prepare a novel microspheres-scaffold hybrid system (CM-ALs) for drug delivery and bone tissue engineering application. The characteristics of CM-ALs scaffolds containing 10% and 20% CH/nHA-AL were evaluated in vitro, including surface morphology and porosity, mechanical properties, drug release, degradation, and osteogenic differentiation. The in vivo bone repair for large segmental radius defects (1.5 cm) in a rabbit model was evaluated by radiography and histology. In vitro study showed more sustained drug release of CM-AL-containing scaffolds than these of CM/nHA-AL and PLLA/nHA/AL scaffolds, and the mechanical and degradation properties of CM-ALs (10%) scaffolds were comparable to that of PLLA/nHA control. The osteogenic differentiation of adipose-derived stem cells (ASCs) was significantly enhanced as indicated by increased alkaline phosphates (ALP) activity and calcium deposition. In vivo study further showed better performance of CM-ALs (10%) scaffolds with complete repair of large-sized bone defects within 8 weeks. A microspheres-scaffold-based release system containing AL-encapsulated chitosan microspheres was successfully fabricated in this study. Our results suggested the promising application of CM-ALs (10%) scaffolds for drug delivery and bone tissue engineering.

摘要

一种基于壳聚糖的微球递送系统已被制备用于控制阿仑膦酸钠(AL)的释放。本研究旨在将载有 AL 的壳聚糖/羟基磷灰石微球(CH/nHA-AL)掺入聚(L-乳酸)/纳米羟基磷灰石(PLLA/nHA)基质中,以制备用于药物输送和骨组织工程应用的新型微球-支架杂化系统(CM-ALs)。体外评估了含有 10%和 20% CH/nHA-AL 的 CM-ALs 支架的特性,包括表面形貌和孔隙率、机械性能、药物释放、降解和成骨分化。通过 X 射线和组织学评估了兔模型中 1.5cm 大段半径缺损的体内骨修复情况。体外研究表明,含有 CM-AL 的支架的药物释放更持久,而 CM/nHA-AL 和 PLLA/nHA/AL 支架的药物释放则更快,且 CM-ALs(10%)支架的机械和降解性能与 PLLA/nHA 对照支架相当。脂肪来源干细胞(ASCs)的成骨分化明显增强,碱性磷酸酶(ALP)活性和钙沉积增加。体内研究进一步表明,CM-ALs(10%)支架具有更好的性能,在 8 周内完全修复了大尺寸的骨缺损。本研究成功制备了含有包封 AL 的壳聚糖微球的基于微球-支架的释放系统。我们的结果表明,CM-ALs(10%)支架在药物输送和骨组织工程方面具有广阔的应用前景。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e295/5428684/0bc2118cdbd2/41598_2017_506_Fig1_HTML.jpg

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