Somvipart Siraporn, Kanokpanont Sorada, Rangkupan Rattapol, Ratanavaraporn Juthamas, Damrongsakkul Siriporn
Department of Chemical Engineering, Faculty of Engineering, Chulalongkorn University, PhayaThai Road, Phatumwan, Bangkok 10330, Thailand.
Int J Biol Macromol. 2013 Apr;55:176-84. doi: 10.1016/j.ijbiomac.2013.01.006. Epub 2013 Jan 16.
Thai silk fibroin and gelatin are attractive biomaterials for tissue engineering and controlled release applications due to their biocompatibility, biodegradability, and bioactive properties. The development of electrospun fiber mats from silk fibroin and gelatin were reported previously. However, burst drug release from such fiber mats remained the problem. In this study, the formation of beads on the fibers aiming to be used for the sustained release of drug was of our interest. The beaded fiber mats were fabricated using electrospinning technique by controlling the solution concentration, weight blending ratio of Thai silk fibroin/gelatin blend, and applied voltage. It was found that the optimal conditions including the solution concentration and the weight blending ratio of Thai silk fibroin/gelatin at 8-10% (w/v) and 70/30, respectively, with the applied voltage at 18 kV provided the fibers with homogeneous formation of beads. Then, the beaded fiber mats obtained were crosslinked by the reaction of carbodiimide hydrochloride (EDC)/N-hydroxysuccinimide (NHS). Methylene blue as a model active compound was loaded on the fiber mats. The release test of methylene blue from the beaded fiber mats was carried out in comparison to that of the smooth fiber mats without beads. It was found that the beaded fiber mats could prolong the release of methylene blue, comparing to the smooth fiber mats without beads. This was possibly due to the beaded fiber mats that would absorb and retain higher amount of methylene blue than the fiber mats without beads. Thai silk fibroin/gelatin beaded fiber mats were established as an effective carrier for the controlled release applications.
泰国丝素蛋白和明胶因其生物相容性、生物降解性和生物活性特性,是用于组织工程和控释应用的有吸引力的生物材料。此前已有关于由丝素蛋白和明胶制备电纺纤维垫的报道。然而,此类纤维垫的药物突发释放问题仍然存在。在本研究中,我们感兴趣的是在纤维上形成珠子以用于药物的持续释放。通过控制溶液浓度、泰国丝素蛋白/明胶共混物的重量混合比和施加电压,使用电纺技术制备了带珠纤维垫。结果发现,最佳条件包括溶液浓度和泰国丝素蛋白/明胶的重量混合比分别为8 - 10%(w/v)和70/30,施加电压为18 kV时,纤维上能均匀形成珠子。然后,通过盐酸碳二亚胺(EDC)/N - 羟基琥珀酰亚胺(NHS)反应对所得带珠纤维垫进行交联。将亚甲基蓝作为模型活性化合物负载在纤维垫上。与无珠的光滑纤维垫相比,对带珠纤维垫上的亚甲基蓝进行释放测试。结果发现,与无珠的光滑纤维垫相比,带珠纤维垫能够延长亚甲基蓝的释放时间。这可能是因为带珠纤维垫比无珠纤维垫能吸收和保留更多量的亚甲基蓝。泰国丝素蛋白/明胶带珠纤维垫被确立为用于控释应用的有效载体。