Reconstructed human skin was prepared from human keratinoblasts. After
1 week of cultivation at the air-liquid interface a stratified layer
developed, similar to native human epidermis. Liposomes with an averag
e diameter of 50 nm, made of phosphatidylcholine (PC), phosphatidylser
ine (PS) and human stratum corneum lipids (hSCL) were applied on top o
f this culture system. The rate of penetration through the reconstruct
ed human epidermis was 1.38, 0.55 and 0.013 ng lipid h(-1) cm(-2) for
PC, hSCL and PS liposomes, respectively. Electron microscopy and confo
cal laser scanning microscopy showed that PS and hSCL liposomes aggreg
ated at the skin surface, while PC liposomes remained homogeneously di
spersed. Fluorescence measurements demonstrated that vesicles, made of
native human stratum corneum lipids rapidly mixed with PS liposomes,
weakly with hSCL liposomes and did not mix with PC liposomes. (C) 1998
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