米诺地尔
脂质体
化学
透皮
药物输送
渗透
离体
体内
皮肤病科
剂型
药品
维甲酸
药理学
生物医学工程
医学
色谱法
维甲酸
膜
有机化学
体外
生物化学
生物技术
生物
基因
作者
Pratiksha Kochar,Kritika Nayak,Shreya Thakkar,Suryanarayana Polaka,Dignesh Khunt,Manju Misra
标识
DOI:10.1080/15569527.2019.1694032
摘要
Purpose: Androgenic alopecia (AGA) is a condition of progressive hair loss and involves follicular miniaturization triggered mainly due to varying levels of androgen besides environmental and genetic factors, which may also play some role. Minoxidil (MXD) has been considered as most effective therapeutic moiety to treat this disorder. Another drug Tretinoin (TRET) is known for its comedolytic activity and is reported to enhance percutaneous absorption of MXD. Presently both these drugs are being utilized for treatment of androgenic alopecia (AGA) in solution form which poses several problems in terms of poor solubility of drug, frequency of application and side effects. Materials and methods: Current work investigates liposomal hydrogel system for simultaneous delivery of MXD and TRET to overcome the limitations of existing formulation. Successful development of liposomes was commenced by thin film hydration method and various parameters affecting desired characteristics like size, morphology, entrapment efficiency; stability and ex vivo permeation were optimized. The formulated liposomes were further characterized for various physicochemical properties and evaluated for in vivo irritancy study in animals. Results and discussion: Results suggested prepared liposomes to be stable, homogenous and capable to hold both the drugs within. Association with hydrogel enhanced the permeation of MXD through skin ex vivo but TRET retained on the skin. Liposome loaded hydrogel was found to be non-irritant to skin. Conclusion: Overall developed system showed potential for effective and simultaneous delivery of both the drugs.
科研通智能强力驱动
Strongly Powered by AbleSci AI