Kathuria Himanshu, Lim Dennis, Cai Junyu, Chung Bong Geun, Kang Lifeng
Department of Pharmacy, National University of Singapore, Singapore 117543, Singapore.
School of Pharmacy, Faculty of Medicine and Health, University of Sydney, Sydney, New South Wales 2006, Australia.
ACS Biomater Sci Eng. 2020 Sep 14;6(9):5061-5068. doi: 10.1021/acsbiomaterials.0c00759. Epub 2020 Aug 19.
Dissolvable microneedle (MN) patches have been widely investigated for transdermal drug delivery. The dissolution rate of MN controls the status of drug release from the MN, which in turn determines drug absorption through skin. However, no systematic approaches have been reported to tune the dissolution profile of dissolvable MN matrices. This is the first study to show polyvinylpyrrolidone (PVP)-based dissolvable MN patches with varying dissolution profiles when PVP is copolymerized with cellulose materials. The MN patches were fabricated through thermal curing and photolithography in tandem. The various grades of pharmaceutical cellulose, such as hydroxypropyl methylcellulose and methyl cellulose, have been investigated as dissolution modifier incorporated in the MN patches. The resultant MN patches had dissolution profiles ranging from 45 min to 48 h. The dissolution rates varied with the grades of cellulose materials. Besides dissolution examination, the MN patches were characterized for their mechanical strength, moisture absorption, and skin penetration efficiency. All of the MN patches were able to penetrate the human skin in vitro. Overall, the PVP MN patches have great potential for skin applications as drug carriers with tunable dissolution profiles.
可溶微针(MN)贴片已被广泛研究用于透皮给药。微针的溶解速率控制着药物从微针中的释放状态,进而决定药物经皮肤的吸收。然而,尚未有系统的方法来调节可溶微针基质的溶解特性。这是第一项展示当聚乙烯吡咯烷酮(PVP)与纤维素材料共聚时,具有不同溶解特性的基于PVP的可溶微针贴片的研究。微针贴片是通过热固化和光刻串联制备的。已研究了各种等级的药用纤维素,如羟丙基甲基纤维素和甲基纤维素,作为掺入微针贴片中的溶解调节剂。所得微针贴片的溶解特性范围为45分钟至48小时。溶解速率随纤维素材料的等级而变化。除了溶解检测外,还对微针贴片的机械强度、吸湿性能和皮肤渗透效率进行了表征。所有微针贴片在体外均能穿透人体皮肤。总体而言,PVP微针贴片作为具有可调溶解特性的药物载体在皮肤应用方面具有巨大潜力。