Bai. Van Den Bergh et al., Interactions of elastic and rigid vesicles with human skin in vitro: electron microscopy and two-photon excitation microscopy, BBA-BIOMEMB, 1461(1), 1999, pp. 155-173
Interactions between vesicle formulations and human skin were studied, in v
itro, in relation to their composition and elasticity. The skin ultrastruct
ure was investigated using transmission electron microscopy (TEM), freeze-f
racture electron microscopy (FFEM) and two-photon fluorescence microscopy (
TPE). The main difference between the vesicle formulations was their elasti
city. Elastic vesicle formulations contained bilayer forming surfactants/li
pids and single-chain surfactant octaoxyethylenelaurate-ester (PEG-8-L), wh
ereas rigid vesicles contained bilayer surfactants in combination with chol
esterol. TEM results showed three types of interactions after non-occlusive
application of elastic PEG-8-L containing vesicle formulations on human sk
in: (1) the presence of spherical lipid structures containing or surrounded
by electron dense spots; (2) oligolamellar vesicles were observed between
the corneocytes in the upper part of the stratum corneum; and (3) large are
as containing lipids, surfactants and electron dense spots were observed de
eper down into the stratum corneum. Furthermore, after treatment with vesic
les containing PEG-8-L and a saturated C12-chain surfactant, small stacks o
f bilayers were found in intercellular spaces of the stratum corneum. Rigid
vesicles affected only the most apical corneocytes to some extent. FFEM ob
servations supported the TEM findings. Major morphological changes in the i
ntercellular lipid bilayer structure were only observed after treatment wit
h PEG-8-L containing elastic vesicles. TPE showed a distinct difference in
penetration pathways after non-occlusive application of elastic or rigid ve
sicles. After treatment with elastic vesicles, threadlike channels were for
med within the entire stratum corneum and the polygonal cell shape of corne
ocytes could not be distinguished. Fluorescent label incorporated in rigid
vesicles was confined to the intercellular spaces of the upper 2-5 mu m of
the stratum corneum and the cell contours could still be distinguished. (C)
1999 Elsevier Science B.V. All rights reserved.