Targeted gene delivery to skin cells in vivo: a comparative study of liposomes and polymers as delivery vehicles.
Targeted gene delivery to skin cells in vivo: a comparative study of liposomes and polymers as delivery vehicles.
复制标题
体内靶向基因递送至皮肤细胞:脂质体和聚合物作为递送载体的比较研究。
DOI:
10.1002/jps.10061
复制
发表时间:
2002
影响因子:
3.8
通讯作者:
Fahl,WilliamE
中科院分区:
文献类型:
--
作者:
Raghavachari,Nalini;Fahl,WilliamE
Liposomes are microscopic lipid membrane vesicles that provide a current strategy for topical, dermal delivery of biologically active molecules. They have been successfully used for the delivery of various low and high molecular weight molecules into the skin, and as an alternative to virus-mediated delivery systems, have opened the field of dermal gene therapy. The present study was undertaken on 6-day-old rat pups to determinein vivothe efficacy of several liposome and nonliposome formulations, including phospholipid liposomes and their cationic or pegylated variants, nonionic liposomes and their cationic variant, PINC polymer (Protective,Interactive,Noncondensing polymers), and a propylene glycol:alcohol:water mixture (delivery vehicle for minoxidil) in delivering β-galactosidase and luciferase reporter genes into skin cells. Based upon our observations of the expression of β-galactosidase and luciferase reporter genes in skin cells, we report here that nonionic liposomes are the most efficient vehicle for transdermal delivery followed by nonionic/cationic and phospholipid (pegylated) liposomes. The propylene glycol:ethanol:water mixture and the PINC polymer were relatively inefficient in the delivery of β-galactosidase or luciferase DNAs. This simple, noninvasive technique of using nonionic liposomes to deliver biomolecules provides an efficient delivery strategy for gene therapy and drug delivery to the dermal organ site. © 2002 Wiley-Liss, Inc. and the American Pharmaceutical Association J Pharm Sci 91:615–622, 2002