Increased skin permeation efficiency of imperatorin via charged ultradeformable lipid vesicles for transdermal delivery

被引:62
作者
Lin, Hongwei [1 ,2 ]
Xie, Qingchun [1 ,2 ]
Huang, Xin [1 ,2 ]
Ban, Junfeng [1 ,2 ]
Wang, Bo [1 ,2 ]
Wei, Xing [3 ]
Chen, Yanzhong [1 ,2 ]
Lu, Zhufen [1 ,2 ]
机构
[1] Guangdong Pharmaceut Univ, Guangdong Prov Key Lab Adv Drug Delivery Syst, Guangzhou, Guangdong, Peoples R China
[2] Guangdong Pharmaceut Univ, Guangdong Prov Engn Ctr Top Precise Drug Delivery, Guangzhou, Guangdong, Peoples R China
[3] Guangdong Shennong Chinese Med Res Inst, Guangzhou, Guangdong, Peoples R China
来源
INTERNATIONAL JOURNAL OF NANOMEDICINE | 2018年 / 13卷
关键词
ultradeformable liposomes; cationic; imperatorin; skin permeation; transdermal drug delivery; TOPICAL DELIVERY; DEFORMABLE LIPOSOMES; SURFACE-CHARGE; DRUG-DELIVERY; IN-VITRO; PENETRATION; CARRIERS; COUMARINS; ACID; FORMULATIONS;
D O I
10.2147/IJN.S150086
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Aim: The aim of this work was to develop a novel vesicular carrier, ultradeformable liposomes (UDLs), to expand the applications of the Chinese herbal medicine, imperatorin (IMP), and increase its transdermal delivery. Methods: In this study, we prepared IMP-loaded UDLs using the thin-film hydration method and evaluated their encapsulation efficiency, vesicle deformability, skin permeation, and the amounts accumulated in different depths of the skin in vitro. The influence of different charged surfactants on the properties of the UDLs was also investigated. Results: The results showed that the UDLs containing cationic surfactants had high entrapment efficiency (60.32%+/- 2.82%), an acceptable particle size (82.4 +/- 0.65 nm), high elasticity, and prolonged drug release. The penetration rate of IMP in cationic-UDLs was 3.45-fold greater than that of IMP suspension, which was the highest value among the vesicular carriers. UDLs modified with cationic surfactant also showed higher fluorescence intensity in deeper regions of the epidermis. Conclusion: The results of our study suggest that cationic surfactant-modified UDLs could increase the transdermal flux, prolong the release of the drug, and serve as an effective dermal delivery system for IMP.
引用
收藏
页码:831 / 842
页数:12
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