Naseri-Nosar Mahdi, Salehi Majid, Hojjati-Emami Shahriar
Department of Biomedical Engineering, Amirkabir University of Technology, Tehran 158754413, Iran.
Department of Tissue Engineering, School of Medicine, Shahroud University of Medical Sciences, Shahroud 3613773955, Iran.
Int J Biol Macromol. 2017 Oct;103:701-708. doi: 10.1016/j.ijbiomac.2017.05.054. Epub 2017 May 15.
The current study aimed to develop a biodegradable three-dimensional drug-loaded scaffold with the core-shell structured fibrils using coaxial wet-electrospinning for neural tissue engineering application. Poly lactic acid was wet-electrospun as the core, whereas cellulose acetate was fabricated into the fibril's shell. The scaffold then was coated with the citalopram-loaded gelatin nanocarriers (CGNs) produced by nanoprecipitation method. Scanning electron microscope observation revealed that the fibrils formed a nonwoven structure with the average diameter of ∼950nm. The particle size measurement by a dynamic light scattering device showed an average diameter of ∼200nm. The porosity measurement via the liquid displacement method showed that the scaffold could not meet the accepted ideal porosity percentage of above 80%, and the measured porosity percentage was ∼60%. The contact angle measurement displayed that the CGN coating made the scaffold highly hydrophilic with a zero degree contact angle. In vitro degradation study in the phosphate buffered saline revealed that the weight of the uncoated scaffold remained relatively constant. However, the CGNs-coated scaffold showed ∼45% weight-loss percentage after 40days. Cytocompatibility evaluation using rat Schwann cells demonstrated that the CGNs-coated scaffold possessed higher cell viability than the uncoated scaffold. Finally, the scaffold was developed into a nerve guidance conduit and surgically implanted in the sciatic nerve defect in Wistar rats. The results of the sciatic functional index, hot plate latency and weight-loss percentage of the wet gastrocnemius muscle, demonstrated that the citalopram-containing scaffold could ameliorate the functional recovery of the sciatic nerve-injured animals which makes it a potential candidate for the neural tissue engineering applications.
当前的研究旨在利用同轴湿法静电纺丝技术开发一种具有核壳结构原纤维的可生物降解三维载药支架,用于神经组织工程应用。聚乳酸被湿法静电纺丝作为核心,而醋酸纤维素则被制成原纤维的外壳。然后,该支架用通过纳米沉淀法制备的载有西酞普兰的明胶纳米载体(CGNs)进行包被。扫描电子显微镜观察显示,原纤维形成了一种平均直径约为950nm的非织造结构。通过动态光散射装置进行的粒径测量显示平均直径约为200nm。通过液体置换法进行的孔隙率测量表明,该支架不符合公认的理想孔隙率百分比(高于80%),测得的孔隙率百分比约为60%。接触角测量显示,CGN包被使支架具有高度亲水性,接触角为零度。在磷酸盐缓冲盐水中进行的体外降解研究表明,未包被的支架重量保持相对恒定。然而,CGNs包被的支架在40天后显示出约45%的失重百分比。使用大鼠雪旺细胞进行的细胞相容性评估表明,CGNs包被的支架比未包被的支架具有更高的细胞活力。最后,该支架被开发成神经导管并手术植入Wistar大鼠的坐骨神经缺损处。坐骨神经功能指数、热板潜伏期和湿腓肠肌失重百分比的结果表明,含西酞普兰的支架可以改善坐骨神经损伤动物的功能恢复,这使其成为神经组织工程应用的潜在候选者。