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Ultradeformable cationic liposomes for delivery of small interfering RNA (siRNA) into human primary melanocytes
被引:66
|作者:
Geusens, B.
[1
]
Lambert, J.
[1
]
De Smedt, S. C.
[2
]
Buyens, K.
[2
]
Sanders, N. N.
[2
,3
]
Van Gele, M.
[1
]
机构:
[1] Ghent Univ Hosp, Dept Dermatol, B-9000 Ghent, Belgium
[2] Univ Ghent, Lab Gen Biochem & Phys Pharm, B-9000 Ghent, Belgium
[3] Univ Ghent, Lab Gene Therapy, Dept Nutr Genet & Ethol, Fac Vet Med, B-9820 Merelbeke, Belgium
关键词:
Ultradeformable liposomes;
Delivery vehicle;
Skin;
Melanocytes;
siRNA;
DRUG CARRIERS;
TRANSDERMAL DELIVERY;
TRIAMCINOLONE-ACETONIDE;
TRANSFECTION EFFICIENCY;
TOPICAL APPLICATION;
INTACT SKIN;
DNA;
VESICLES;
EXPRESSION;
IMMUNIZATION;
D O I:
10.1016/j.jconrel.2008.10.003
中图分类号:
O6 [化学];
学科分类号:
0703 ;
摘要:
The aim of this work was to develop a system that can deliver siRNA into cells present in the human epidermis. More specifically, we wanted to block the expression of a specific Myosin Va exon F containing isoform that is physiologically involved in melanosome transport in human melanocytes. Therefore, we prepared and investigated the capacity of ultradeformable cationic liposomes (UCLs) to deliver siRNA in hard-to-transfect human primary melanocytes. UCLs were formulated from different w:w ratios (6:1, 8:1 and 10:1) of the cationic lipid 1,2-dioleoyl-3-trimethylammonium propane (DOTAP) and the edge activator sodium cholate. Subsequently, UCL/siRNA complexes were prepared and their particle size, surface charge, deformability, cytotoxicity, transfection efficiency and long-term stability were tested. The best results were obtained with UCLs composed of a DOTAP/NaChol ratio of 6:1 (w:w) which are promising for future in vivo experiments. (C) 2008 Elsevier B.V. All rights reserved.
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页码:214 / 220
页数:7
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