Lee Hoik, Xu Gang, Kharaghani Davood, Nishino Masayoshi, Song Kyung Hun, Lee Jung Soon, Kim Ick Soo
Nano Fusion Technology Research Group, Division of Frontier Fibers, Institute for Fiber Engineering (IFES), Interdisciplinary Cluster for Cutting Edge Research (ICCER), Shinshu University, Tokida 3-15-1, Ueda, Nagano, 386-8567, Japan.
Department of Clothing & Textiles, Pai Chai University, Daejeon, 35345, South Korea.
Int J Pharm. 2017 Oct 5;531(1):101-107. doi: 10.1016/j.ijpharm.2017.08.081. Epub 2017 Aug 19.
Simple sequential electrospinning was utilized to create a functional tri-layered nanofiber mesh that achieves time-regulated biphasic drug release behavior. A tri-layered nanofiber mesh -composed of zein and poly(vinylpyrrolidone) (PVP) as the top/bottom and middle layers, respectively - was constructed through sequential electrospinning with ketoprofen (KET) as the model drug. PVP was blended with graphene oxide (GO) to improve the drug release functionality of PVP nanofiber as well as its mechanical properties. Scanning electron microscopy confirmed that the resultant nanofibers had a linear morphology, smooth surface, and tri-layered structure. In addition, X-ray diffraction patterns, differential scanning calorimetric analyses, and Fourier transform infrared spectra verified that the drugs were uniformly dispersed throughout the nanofiber due to good compatibility between the polymer and KET induced by hydrogen interaction. In vitro release test of the tri-layered structure, each component of which had distinct release features, successfully demonstrated time-regulated biphasic drug release. Also, it was confirmed that the drug release rate and duration can be controlled by designing a morphological feature - namely, mesh thickness - which was achieved by simply regulating the spinning time of the first and third layer. This multilayered electrospun nanofiber mesh fabricated by sequential electrospinning could provide a useful method of controlling drug release behavior over time, which will open new routes for practical applications and stimulate further research in the development of effective drug release carriers.
采用简单的连续静电纺丝法制备了一种功能性三层纳米纤维网,该纳米纤维网具有时间调控的双相药物释放行为。以玉米醇溶蛋白和聚乙烯吡咯烷酮(PVP)分别作为顶层/底层和中间层,通过连续静电纺丝制备了一种三层纳米纤维网,并以酮洛芬(KET)作为模型药物。将PVP与氧化石墨烯(GO)混合,以改善PVP纳米纤维的药物释放功能及其机械性能。扫描电子显微镜证实,所得纳米纤维具有线性形态、光滑表面和三层结构。此外,X射线衍射图谱、差示扫描量热分析和傅里叶变换红外光谱证实,由于聚合物与KET之间通过氢键相互作用具有良好的相容性,药物均匀地分散在整个纳米纤维中。对三层结构进行体外释放测试,其各组分具有不同的释放特性,成功地证明了时间调控的双相药物释放。此外,还证实了药物释放速率和持续时间可以通过设计形态特征(即网厚度)来控制,这可以通过简单地调节第一层和第三层的纺丝时间来实现。通过连续静电纺丝制备的这种多层电纺纳米纤维网可以提供一种控制药物随时间释放行为的有用方法,这将为实际应用开辟新的途径,并刺激在有效药物释放载体开发方面的进一步研究。