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首页> 外文期刊>Journal of biomedical materials research, Part A >Porous Scaffolds of Gelatin-Hydroxyapatite Nanocomposites Obtained by Biomimetic Approach: Characterization and Antibiotic Drug Release
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Porous Scaffolds of Gelatin-Hydroxyapatite Nanocomposites Obtained by Biomimetic Approach: Characterization and Antibiotic Drug Release

机译:通过仿生方法获得的明胶-羟基磷灰石纳米复合材料的多孔支架:表征和抗生素药物释放。

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Gelatin-hydroxyapatite (HA) nanocomposite porous scaffolds were fabricated biomimetically, and their feasibility as a drug-delivery carrier for tissue-regeneration and wound-healing treatments was addressed. The composite sols were prepared by the precipitation of HA up to 30 wt percent within a gelatin solution with the use of calcium and phosphate precursors, and the porous scaffold was obtained by casting the sols and further freeze drying. The obtained bodies were crosslinked with carbodiimide derivatives to retain chemical and thermal integrity. The apatite precipitates were observed to be a poorly crystallized carbonate-substituted HA. The nanocomposite scaffolds had porosities of approx 89-92 percent and exhibited a bimodal pore distribution, that is, the macropores (approx 300-500 mum) of the framework structure, and micropores (approx 0.5-1 mum) formed on the framework surface. Transmission electron microscopy (TEM) observation revealed the precipitation of highly elongated HA nanocrystals on the gelatin network. The well-developed porous structure and organized nanocomposite configurations were in marked contrast to the directly mixed gelatin-HA powder conventional composites. For drug-release tests, tetracycline, an antibiotic drug, was entrapped within the scaffold, and the drug-release profile was examined with processing parameters, such as HA amount in gelatin, crosslinking degree, and initial drug addition. The drug entrapment decreased with increasing HA amount, but increased with increasing crosslinking degree and initial drug addition. The crosslinking of the gelatin was the prerequisite to sustaining and controlling the drug releases. Compared to pure gelatin, the gelat-in-HA nanocomposites had lower drug releases, because of their lower water uptake and degradation. All the nanocomposite scaffolds released drugs in proportion to the initial drug addition, suggesting their capacity to deliver drugs in a controlled manner. Based on the findings of the well-developed morphological feature and controlled drug-release profile, the gelatin-HA nanocomposite porous scaffolds are suggested to be potentially useful for hard-tissue regeneration.
机译:仿生制备明胶-羟基磷灰石(HA)纳米复合多孔支架,并探讨了其作为组织再生和伤口愈合治疗的药物递送载体的可行性。通过使用钙和磷酸盐前体在明胶溶液中沉淀高达30 wt%的HA来制备复合溶胶,并通过浇铸溶胶并进一步冷冻干燥获得多孔支架。将获得的物体与碳二亚胺衍生物交联以保持化学和热完整性。观察到磷灰石沉淀物是结晶性差的碳酸盐取代的HA。纳米复合支架的孔隙率约为89-92%,并显示出双峰孔分布,即骨架结构的大孔(约300-500μm)和在骨架表面形成的微孔(约0.5-1μm)。透射电子显微镜(TEM)的观察显示明胶网络上高度伸长的HA纳米晶体的沉淀。发达的多孔结构和有组织的纳米复合材料构型与直接混合的明胶-HA粉末常规复合材料形成鲜明对比。对于药物释放测试,将四环素(一种抗生素药物)截留在支架中,并通过加工参数(例如明胶中的HA量,交联度和初始药物添加)检查药物释放曲线。随着HA量的增加,药物截留量减少,但是随着交联度和初始药物添加量的增加,药物截留量增加。明胶的交联是维持和控制药物释放的前提。与纯明胶相比,HA中明胶纳米复合物的吸水率和降解率较低,因此具有较低的药物释放。所有的纳米复合材料支架都与最初添加的药物成比例地释放药物,表明它们以受控方式递送药物的能力。基于良好发展的形态学特征和受控药物释放曲线的发现,明胶-HA纳米复合多孔支架被认为对硬组织再生具有潜在的用途。

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