Effect of edge activators on the formation and transfection efficiency of ultradeformable liposomes

被引:111
作者
Lee, EH
Kim, A
Oh, YK
Kim, CK
机构
[1] Seoul Natl Univ, Coll Pharm, Natl Res Lab Drug & Gene Delivery, Kwanak Gu, Seoul 151742, South Korea
[2] Pochon CHA Univ, Coll Med, Dept Microbiol, Kyonggi Do 487800, South Korea
[3] Pochon CHA Univ, Coll Med, Inst Med Res, Kyonggi Do 487800, South Korea
关键词
transdermal gene delivery; ultradeformable liposomes; edge activators; plasmid DNA;
D O I
10.1016/j.biomaterials.2004.02.020
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Highly deformable hydrophilic lipid vesicles have been studied for transdermal delivery of therapeutically active small molecules and proteins. Here, we report the effects of edge activators on the formation of ultradeformable liposomes (UL) and transdermal gene delivery. Sodium cholate, sodium deoxycholate, and Tween 80 were tested as edge activators. Of the edge activators, sodium cholate and sodium deoxycholate resulted in the smaller sizes of UL and more positive zeta potentials than did Tween 80. Moreover, sodium deoxycholate-based UL showed the highest positive zeta potentials, which might lead to the firmer binding with negatively charged DNA. Following topical application onto mice, DNA complexed with UL containing either sodium cholate or sodium deoxycholate showed substantial transdermal absorption. In contrast, DNA complexed with Tween 80-based UL did not show in vivo transdermal absorption. These data suggest that UL might be of use as a transdermal delivery system of plasmid DNA, and that the choice of edge activators may play an important, role in the transdermal delivery of plasmid DNA via UL. (C) 2004 Elsevier Ltd. All rights reserved.
引用
收藏
页码:205 / 210
页数:6
相关论文
共 23 条
[1]   Novel mechanisms and devices to enable successful transdermal drug delivery [J].
Barry, BW .
EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES, 2001, 14 (02) :101-114
[2]   Skin structure and mode of action of vesicles [J].
Bouwstra, JA ;
Honeywell-Nguyen, PL .
ADVANCED DRUG DELIVERY REVIEWS, 2002, 54 :S41-S55
[3]   LIPID VESICLES PENETRATE INTO INTACT SKIN OWING TO THE TRANSDERMAL OSMOTIC GRADIENTS AND HYDRATION FORCE [J].
CEVC, G ;
BLUME, G .
BIOCHIMICA ET BIOPHYSICA ACTA, 1992, 1104 (01) :226-232
[4]   Ultraflexible vesicles, transfersomes, have an extremely low pore penetration resistance and transport therapeutic amounts of insulin across the intact mammalian skin [J].
Cevc, G ;
Gebauer, D ;
Stieber, J ;
Schätzlein, A ;
Blume, G .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES, 1998, 1368 (02) :201-215
[5]   Biological activity and characteristics of triamcinolone-acetonide fon-nulated with the self-regulating drug carriers, Transfersomes® [J].
Cevc, G ;
Blume, G .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES, 2003, 1614 (02) :156-164
[6]   TRANSDERMAL DRUG CARRIERS - BASIC PROPERTIES, OPTIMIZATION AND TRANSFER EFFICIENCY IN THE CASE OF EPICUTANEOUSLY APPLIED PEPTIDES [J].
CEVC, G ;
SCHATZLEIN, A ;
BLUME, G .
JOURNAL OF CONTROLLED RELEASE, 1995, 36 (1-2) :3-16
[7]   Transfersomes-mediated transepidermal delivery improves the regio-specificity and biological activity of corticosteroids in vivo [J].
Cevc, G ;
Blume, G ;
Schatzlein, A .
JOURNAL OF CONTROLLED RELEASE, 1997, 45 (03) :211-226
[8]   Oestradiol skin delivery from ultradeformable liposomes: refinement of surfactant concentration [J].
El Maghraby, GMM ;
Williams, AC ;
Barry, BW .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2000, 196 (01) :63-74
[9]   Iontophoretic estradiol skin delivery and tritium exchange in ultradeformable liposomes [J].
Essa, EA ;
Bonner, MC ;
Barry, BW .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2002, 240 (1-2) :55-66
[10]   Characterization of silica-coated hematite and application to the formation of composite particles including egg yolk PC liposomes [J].
Furusawa, K ;
Matsumura, H ;
Majima, T .
JOURNAL OF COLLOID AND INTERFACE SCIENCE, 2003, 264 (01) :95-100