Transdermal delivery of capsaicin derivative-sodium nonivamide acetate using microemulsions as vehicles

被引:84
作者
Bin Huang, Yaw [2 ]
Lin, Yong Hao [1 ]
Lu, Tzy Ming [3 ]
Wang, Ren Jiunn [1 ]
Tsai, Yi Hung [1 ]
Wu, Pao Chu [1 ]
机构
[1] Kaohsiung Med Univ, Fac Pharm, Kaohsiung 80708, Taiwan
[2] Kaohsiung Med Univ, Grad Inst Clin Pharm, Kaohsiung 80708, Taiwan
[3] Tajen Univ Technol, Dept Pharm, Yanpushiang 907, Pingtung, Taiwan
关键词
sodium nonivamide acetate; microemulsion; transdermal delivery; isopropyl myristate; viscosity;
D O I
10.1016/j.ijpharm.2007.07.022
中图分类号
R9 [药学];
学科分类号
1007 [药学];
摘要
The objective of this study was to prepare sodium nonivamide acetate (SNA) microemulsion for topical administration. Microemulsions consisted of a mixed surfactant of Tween 80 and Span 20 as surfactant, ethanol as cosurfactant, isopropyl myristate (IPM) as an oil phase and water as an external phase. The effect of composition of microemulsion including the ratio of oil phase/surfactant/aqueous phase, various cosurfactant and polymer on the character and permeability of microemulsion were evaluated. The mean droplet size of SNA microemulsions ranged from 64 to 208 nm. Microemulsions showed potent enhancement effect for SNA transdermal delivery by a 3.7-7.1-fold increase when compared with the control group. Microemulsion containing ethanol as cosurfactant had the highest enhancement effect. With incorporated polymer, the viscosity of microemulsions increased resulting in the decrease in penetration rate of SNA. However, the permeability of SNA delivered from microemulsion was higher than SNA from volatile vehicles (pH 4.2 buffer containing 25% ethanol) reported in an earlier study, therefore microemulsions could be an effective vehicle for topical delivery of SNA. (c) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:206 / 211
页数:6
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