将含有纳米二氧化硅颗粒的环丙沙星壳聚糖基纳米复合水凝胶作为骨组织工程应用支架

IF 6.2 Q1 CHEMISTRY, APPLIED
Soheila Zare , Morteza Eskandani , Somayeh Vandghanooni , Hadi Hossainpour , Mehdi Jaymand
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引用次数: 0

摘要

考虑到天然骨的纳米复合结构,基于骨传导(纳米)材料和高分子生物材料的三维(3D)纳米复合水凝胶是骨组织工程(TE)中前景广阔的支架。因此,一种由壳聚糖(CS)、聚(2-羟乙基甲基丙烯酸酯)(PHEMA)和二氧化硅纳米颗粒(NPs)组成的新型支架被制作出来,用于骨组织工程(TE)。首先合成 SiO2 NPs,然后对其进行修饰。在有交联剂存在的情况下,通过自由基聚合法将修饰过的 NPs、CS 和 HEMA 单体共聚成纳米复合水凝胶(CS-cl-PHEMA/SiO2),然后加入抗生素药物环丙沙星(Cip)。该支架的药物封装效率约为 20%,体外药物释放研究表明,该支架的药物释放曲线与 pH 值有关。研究人员从许多物理化学和生物学特征方面考察了该支架在骨 TE 中的适用性。5 小时后,支架的最大膨胀率达到 312%,随后达到平衡。该支架在体外生物降解方面表现良好,尤其是在酸性 pH 条件下。溶血试验表明,该支架的血液相容性高达 400 µgmL-1,溶血率为 4.9%。MTT 分析结果表明,该支架对细胞没有任何毒性作用,并能促进成骨细胞的增殖。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Ciprofloxacin-loaded chitosan-based nanocomposite hydrogel containing silica nanoparticles as a scaffold for bone tissue engineering application

Ciprofloxacin-loaded chitosan-based nanocomposite hydrogel containing silica nanoparticles as a scaffold for bone tissue engineering application

Considering the nanocomposite structure of natural bone, three-dimensional (3D) nanocomposite hydrogels based on osteoconductive (nano-)materials and polymeric biomaterials are promising scaffolds in bone tissue engineering (TE). Therefore, a novel scaffold composed of chitosan (CS), poly(2-hydroxyethyl methacrylate) (PHEMA), and SiO2 nanoparticles (NPs) was fabricated for bone TE application. Firstly, SiO2 NPs were synthesized, and then modified. The modified NPs, CS, and HEMA monomer was copolymerized via free radical polymerization method in the presence of a crosslinker to afford a nanocomposite hydrogel (CS-cl-PHEMA/SiO2) followed by loading of ciprofloxacin (Cip) as an antibiotic drug. Drug encapsulation efficiency was obtained approximately 20% for the scaffold, and in vitro drug release study revealed that the scaffold had a pH-dependent drug release profile. Applicability of the scaffold in bone TE was examined in terms of numerous physicochemical and biological features. Maximum swelling of scaffold was obtained as 312% after 5 h, and then reached equilibrium. The scaffold exhibited proper in vitro biodegradation, especially in acidic pH. Hemolysis assay revealed that the scaffold was hemocompatible up to 400 µgmL−1 with hemolytic rate of 4.9%. MTT-assay results revealed that the scaffold do not had any toxic effects on the cells and can improve the proliferation of osteoblast cells.

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