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载铜多功能羧甲基壳聚糖/海藻酸钠支架用于消除临床细菌感染和促进骨形成。

Multifunctional Copper-Containing Carboxymethyl Chitosan/Alginate Scaffolds for Eradicating Clinical Bacterial Infection and Promoting Bone Formation.

机构信息

Southern Medical University , No. 1023 Shatai Road, Guangzhou, Guangdong 510515, China.

Guangdong Key Lab of Orthopedic Technology and Implant Materials, Key Laboratory of Trauma & Tissue Repair of Tropical Area of PLA, Department of Orthopedics, Guangzhou General Hospital of Guangzhou Military Command , No. 111 Liuhua Road, Guangzhou, Guangdong 510010, China.

出版信息

ACS Appl Mater Interfaces. 2018 Jan 10;10(1):127-138. doi: 10.1021/acsami.7b13750. Epub 2017 Dec 19.

Abstract

Repairing infected bone defects relies on a scaffold that can not only fill the defects to promote bone formation but also kill clinically present bacterial pathogens such as Staphylococcus aureus (S. aureus). To meet this demand, here, we develop a new copper (Cu) containing natural polymeric scaffold with a full potential for repairing infected bone defects. Instead of directly adding antibacterial Cu ions to the polymer mixtures, which caused uncontrolled polymer cross-linking, we added Cu nanoparticles to the mixture of anionic carboxymethyl chitosan (CMC) and alginate (Alg). Then, the Cu ions released from the Cu nanoparticles gradually cross-linked the polymer mixtures, which was further turned into a scaffold (CMC/Alg/Cu) with an interconnected porous structure by freeze-drying. We found that the CMC/Alg/Cu scaffolds showed significantly improved capabilities of osteogenesis and killing clinical bacteria compared to CMC/Alg scaffolds fabricated by the same procedure but without adding Cu nanoparticles. Specifically, in vitro studies showed that the CMC/Alg/Cu scaffolds with excellent biocompatibility could enhance preosteoblastic cell adhesion by upregulating the expression level of adhesion-related genes (focal adhesion kinase (FAK), paxillin (PXN), and vinculin (VCL)), promoting osteogenic differentiation and mineralization by upregulating the osteogenesis-related gene expression and extracellular calcium deposition. In vivo studies further demonstrated that CMC/Alg/Cu scaffolds could induce the formation of vascularized new bone tissue in 4 weeks while avoiding clinical bacterial infection even when the implantation sites were challenged with the clinically collected S. aureus bacteria. This work represents a facile and innovative approach to the fabrication of Cu containing polymer scaffolds that can potentially be used to repair infected bone defects.

摘要

修复感染性骨缺损依赖于一种支架,它不仅能填充缺损以促进骨形成,还能杀死金黄色葡萄球菌(S. aureus)等临床存在的细菌病原体。为了满足这一需求,我们开发了一种新的含铜(Cu)天然聚合物支架,具有修复感染性骨缺损的巨大潜力。我们没有像直接将抗菌 Cu 离子添加到聚合物混合物中那样,导致不可控的聚合物交联,而是将 Cu 纳米粒子添加到阴离子羧甲基壳聚糖(CMC)和藻酸盐(Alg)的混合物中。然后,Cu 纳米粒子释放的 Cu 离子逐渐交联聚合物混合物,通过冷冻干燥进一步将其转化为具有互连通孔结构的支架(CMC/Alg/Cu)。我们发现,与通过相同程序但不添加 Cu 纳米粒子制造的 CMC/Alg 支架相比,CMC/Alg/Cu 支架在成骨和杀死临床细菌方面的能力有显著提高。具体而言,体外研究表明,具有良好生物相容性的 CMC/Alg/Cu 支架可以通过上调粘附相关基因(粘着斑激酶(FAK)、桩蛋白(PXN)和 vinculin(VCL))的表达水平来增强前成骨细胞的粘附,通过上调成骨相关基因的表达和细胞外钙沉积来促进成骨分化和矿化。体内研究进一步证明,CMC/Alg/Cu 支架可以在 4 周内诱导血管化新骨组织的形成,同时避免临床细菌感染,即使植入部位受到临床收集的金黄色葡萄球菌细菌的挑战。这项工作代表了一种制造含 Cu 聚合物支架的简便而创新的方法,该方法可能用于修复感染性骨缺损。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b67f/5764773/22f6280a8b18/nihms931392f1.jpg

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