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静电纺丝聚乙烯醇纳米纤维作为咖啡因和核黄素的口服速溶给药系统。

Electrospun polyvinyl-alcohol nanofibers as oral fast-dissolving delivery system of caffeine and riboflavin.

机构信息

Technical University of Denmark, DTU Food, Søltofts Plads, B227, 2800 Kgs. Lyngby, Denmark.

出版信息

Colloids Surf B Biointerfaces. 2013 Mar 1;103:182-8. doi: 10.1016/j.colsurfb.2012.10.016. Epub 2012 Oct 17.

Abstract

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.

摘要

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%)。

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