Pig skin structure and transdermal delivery of liposomes: A two photon microscopy study

被引:97
作者
Carrer, Dolores C. [1 ]
Vermehren, Charlotte [2 ]
Bagatolli, Luis A. [1 ]
机构
[1] Univ So Denmark, Dept Biochem & Mol Biol, Memphys Ctr Biomembrane Phys, Membrane Biophys & Biophoton Grp, DK-5230 Odense, Denmark
[2] Leo Pharma AS, Ballerup, Denmark
基金
新加坡国家研究基金会;
关键词
Pig skin; Two photon microscopy; Flexible liposomes; LAURDAN; Transdermal drug delivery;
D O I
10.1016/j.jconrel.2008.08.006
中图分类号
O6 [化学];
学科分类号
0703 [化学];
摘要
In this work we have characterized the architecture and physical properties of pig skin epidermis including its permeability to different liposome formulations. Autofluorescence images show that cells in the epidermis, from the basal layer to the stratum corneum, are organized in clusters that are in turn separated by particular structures we named "canyons". These canyons start in the surface as a wrinkle, eventually closing and going all the way inside the epidermis as a distinct structure that reaches the stratum basale. This structure, described previously in the epidermis of mouse skin as "intercluster pathway", was suggested to be filled with an unknown material and offer low resistance to vesicle penetration. Analysis of LAURDAN Generalized Polarization images of pig skin show that the canyons are filled with a non-polar poorly hydrated material, similar to that observed in pig skin stratum corneum. These results together with the data obtained from skin autofluorescence images suggest that these canyons are invaginations/extension of SC material. Fluorescently labeled lipids incorporated into very flexible liposomes are able to penetrate into the skin, eventually reaching the basal layer and the dermis plane. The presence of charged lipids in the liposomes enhances size stability and thus the efficiency of penetration. (C) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:12 / 20
页数:9
相关论文
共 45 条
[1]
Two photon fluorescence microscopy of coexisting lipid domains in giant unilamellar vesicles of binary phospholipid mixtures [J].
Bagatolli, LA ;
Gratton, E .
BIOPHYSICAL JOURNAL, 2000, 78 (01) :290-305
[2]
To see or not to see: Lateral organization of biological membranes and fluorescence microscopy [J].
Bagatolli, Luis A. .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES, 2006, 1758 (10) :1541-1556
[3]
Interaction of liposome formulations with human skin in vitro [J].
Betz, G ;
Imboden, R ;
Imanidis, G .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2001, 229 (1-2) :117-129
[4]
Structure of the skin barrier and its modulation by vesicular formulations [J].
Bouwstra, JA ;
Honeywell-Nguyen, PL ;
Gooris, GS ;
Ponec, M .
PROGRESS IN LIPID RESEARCH, 2003, 42 (01) :1-36
[5]
Skin structure and mode of action of vesicles [J].
Bouwstra, JA ;
Honeywell-Nguyen, PL .
ADVANCED DRUG DELIVERY REVIEWS, 2002, 54 :S41-S55
[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]
Ultradeformable lipid vesicles can penetrate the skin and other semi-permeable barriers unfragmented.: Evidence from double label CLSM experiments and direct size measurements [J].
Cevc, G ;
Schätzlein, A ;
Richardsen, H .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES, 2002, 1564 (01) :21-30
[8]
2-PHOTON LASER SCANNING FLUORESCENCE MICROSCOPY [J].
DENK, W ;
STRICKLER, JH ;
WEBB, WW .
SCIENCE, 1990, 248 (4951) :73-76
[9]
DIASPRO A, 2002, CONFOCAL 2 PHOTON MI, P39
[10]
Lipid vesicles for skin delivery of drugs: Reviewing three decades of research [J].
Elsayed, Mustafa M. A. ;
Abdallah, Ossama Y. ;
Naggar, Viviane F. ;
Khalafallah, Nawal M. .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2007, 332 (1-2) :1-16