Preparation and Characterization of a Lecithin Nanoemulsion as a Topical Delivery System

被引:89
作者
Zhou, Huafeng [1 ,2 ]
Yue, Yang [1 ]
Liu, Guanlan [1 ]
Li, Yan [1 ]
Zhang, Jing [1 ]
Gong, Qiu [1 ]
Yan, Zemin [2 ]
Duan, Mingxing [1 ]
机构
[1] Tsinghua Univ, Sch Life Sci, State Key Lab Biomembrane & Membrane Biotechnol, Beijing 100084, Peoples R China
[2] Jiangsu Longliqi Biosci Co Ltd, Suzhou 215555, Peoples R China
来源
NANOSCALE RESEARCH LETTERS | 2010年 / 5卷 / 01期
关键词
Lecithin; Nanoemulsion; Fluorescence; Topical delivery system; Skin hydration; SUBMICRON EMULSIONS; CARRIERS; MICROEMULSIONS; HYDRATION;
D O I
10.1007/s11671-009-9469-5
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Purpose of this study was to establish a lecithin nanoemulsion (LNE) without any synthetic surfactant as a topical delivery vehicle and to evaluate its topical delivery potential by the following factors: particle size, morphology, viscosity, stability, skin hydration and skin penetration. Experimental results demonstrated that an increasing concentration of soybean lecithin and glycerol resulted in a smaller size LNE droplet and increasing viscosity, respectively. The droplet size of optimized LNE, with the glycerol concentration above 75% (w/w), changed from 92 (F10) to 58 nm (F14). Additionally, LNE, incorporated into o/w cream, improved the skin hydration capacity of the cream significantly with about 2.5-fold increase when the concentration of LNE reached 10%. LNE was also demonstrated to improve the penetrability of Nile red (NR) dye into the dermis layer, when an o/w cream, incorporated with NR-loaded LNE, applied on the abdominal skin of rat in vivo. Specifically, the arbitrary unit (ABU) of fluorescence in the dermis layer that had received the cream with a NR-loaded LNE was about 9.9-fold higher than the cream with a NR-loaded general emulsion (GE). These observations suggest that LNE could be used as a promising topical delivery vehicle for lipophilic compounds.
引用
收藏
页码:224 / 230
页数:7
相关论文
共 37 条
[1]  
Bajoria R, 1998, PLACENTA, V19, P265
[2]   Novel mechanisms and devices to enable successful transdermal drug delivery [J].
Barry, BW .
EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES, 2001, 14 (02) :101-114
[3]   Breaching the skin's barrier to drugs [J].
Barry, BW .
NATURE BIOTECHNOLOGY, 2004, 22 (02) :165-167
[4]   Cationic submicron emulsions for pulmonary DNA immunization [J].
Bivas-Benita, M ;
Oudshoorn, M ;
Romeijn, S ;
van Meijgaarden, K ;
Koerten, H ;
van der Meulen, H ;
Lambert, G ;
Ottenhoff, T ;
Benita, S ;
Junginger, H ;
Borchard, G .
JOURNAL OF CONTROLLED RELEASE, 2004, 100 (01) :145-155
[5]   Morphology of semisolid aqueous phosphatidylcholine dispersions, a freeze fracture electron microscopy study [J].
Brandl, M ;
Drechsler, M ;
Bachmann, D ;
Bauer, KH .
CHEMISTRY AND PHYSICS OF LIPIDS, 1997, 87 (01) :65-72
[6]   Lipid vesicles and other colloids as drug carriers on the skin [J].
Cevc, G .
ADVANCED DRUG DELIVERY REVIEWS, 2004, 56 (05) :675-711
[7]   Hydration-driven transport of deformable lipid vesicles through fine pores and the skin barrier [J].
Cevc, G ;
Gebauer, D .
BIOPHYSICAL JOURNAL, 2003, 84 (02) :1010-1024
[8]   Influence of glycerol and sorbitol on thermally induced droplet aggregation in oil-in-water emulsions stabilized by β-lactoglobulin [J].
Chanasattru, Wanlop ;
Decker, Eric A. ;
McClements, D. Julian .
FOOD HYDROCOLLOIDS, 2009, 23 (02) :253-261
[9]   Aerosol-OT microemulsions as transdermal carriers of tetracaine hydrochloride [J].
Changez, M ;
Varshney, M .
DRUG DEVELOPMENT AND INDUSTRIAL PHARMACY, 2000, 26 (05) :507-512
[10]  
DIANE S, 1984, INT J PHARMACEUT, V22, P291, DOI DOI 10.1016/0378-5173(84)90029-2