Technical University of Denmark, DTU Food, Søltofts Plads, B227, 2800 Kgs. Lyngby, Denmark.
Colloids Surf B Biointerfaces. 2013 Mar 1;103:182-8. doi: 10.1016/j.colsurfb.2012.10.016. Epub 2012 Oct 17.
Fast-dissolving drug delivery systems were prepared by electrospinning using polyvinyl alcohol (PVA) as the filament-forming polymer and drug carrier. Caffeine and riboflavin were used as the model drugs. Scanning electron microscopy (SEM), Fourier-transform infrared (FTIR) and X-ray diffraction were applied to investigate the physicochemical properties of electrospun nanofibers. The SEM images showed that nanofibers prepared from electrospinning PVA/drug aqueous solutions possessed an ultrafine morphology with an average diameter in the range of 260-370 nm. Pharmacotechnical tests showed that PVA/caffeine and PVA/riboflavin nanofibrous mats had almost the same dissolution time (about 1.5 s) and wetting time (about 4.5 s). The release measurements indicated that drugs can be released in a burst manner (caffeine to an extent of 100% and riboflavin to an extent of 40% within 60 s) from the PVA nanofibrous matrices.
采用静电纺丝法制备了以聚乙烯醇(PVA)为成丝聚合物和药物载体的速溶药物传递系统。咖啡因和核黄素被用作模型药物。扫描电子显微镜(SEM)、傅里叶变换红外(FTIR)和 X 射线衍射用于研究电纺纳米纤维的物理化学性质。SEM 图像表明,由电纺 PVA/药物水溶液制备的纳米纤维具有超细形态,平均直径在 260-370nm 范围内。药剂学测试表明,PVA/咖啡因和 PVA/核黄素纳米纤维垫具有几乎相同的溶解时间(约 1.5s)和润湿时间(约 4.5s)。释放测量表明,药物可以从 PVA 纳米纤维基质中以爆发的方式释放(咖啡因在 60s 内释放 100%,核黄素释放 40%)。