School of Chemical Engineering and Technology, Tianjin University, Tianjin, 300072, China.
J Mater Sci Mater Med. 2013 Feb;24(2):333-41. doi: 10.1007/s10856-012-4805-1. Epub 2012 Nov 9.
To improve the poor compatibility among different components of Drug-in-adhesive type patch, two novel plasters (Drug-in-fiber and Drug-in-adhesive/fiber) were developed based on ibuprofen (IBU)-loaded fiber mats. These fibrous mats were fabricated via electrospinning of cellulose acetate/poly(vinylpyrrolidone) composites in a binary solvent of N,N-dimethyl acetamide/acetone. Physical status studies suggested that Drug-in-fiber could inhibit IBU re-crystallization, but the active ingredients were released at a relatively slow rate due to the dual-resistance of fiber mat and adhesive matrix. To overcome this shortcoming, Drug-in-adhesive/fiber was designed by coupling medicated hydrophilic pressure sensitive adhesive and IBU-loaded fiber mat. This method endowed Drug-in-adhesive/fiber a fast IBU release rate and high permeated drug amount though simulative skins. This design separated enhancer from adhesive matrix, which guaranteed Drug-in-adhesive/fiber excellent adhesion forces. Hence, the plasters based on medicated fiber mats improved the compatibility among patch components.
为了改善药物贴剂中不同成分之间的相容性差的问题,我们基于布洛芬(IBU)负载纤维垫开发了两种新型膏药(纤维内药物和纤维内药物/胶内药物)。这些纤维垫是通过醋酸纤维素/聚乙烯吡咯烷酮复合材料在 N,N-二甲基乙酰胺/丙酮的二元溶剂中静电纺丝制备的。物理状态研究表明,纤维内药物可以抑制 IBU 再结晶,但由于纤维垫和胶内基质的双重阻力,活性成分的释放速度相对较慢。为了克服这一缺点,我们通过将含药亲水性压敏胶和 IBU 负载纤维垫偶联设计了纤维内药物/胶内药物。该方法使纤维内药物/胶内药物具有较快的 IBU 释放速度和较高的透皮药物量,尽管是模拟皮肤。这种设计将增强剂与胶内基质分离,保证了纤维内药物/胶内药物具有优异的黏附力。因此,基于含药纤维垫的膏药提高了贴剂各成分之间的相容性。