Motoyama Keiichi, Nakashima Yoshihiro, Aramaki Yukihiko, Hirayama Fumitoshi, Uekama Kaneto, Arima Hidetoshi
Graduate School of Pharmaceutical Sciences, Kumamoto University, 5-1 Oe-honmachi, Kumamoto 862-0973, Japan.
J Drug Deliv. 2011;2011:476137. doi: 10.1155/2011/476137. Epub 2010 Dec 9.
The purpose of this study is to evaluate in vitro gene delivery mediated by asialofetuin-appended cationic liposomes (AF-liposomes) associating cyclodextrins (CyD/AF-liposomes) as a hepatocyte-selective nonviral vector. Of various CyDs, AF-liposomes associated with plasmid DNA (pDNA) and γ-cyclodextrin (γ-CyD) (pDNA/γ-CyD/AF-liposomes) showed the highest gene transfer activity in HepG2 cells without any significant cytotoxicity. In addition, γ-CyD enhanced the encapsulation ratio of pDNA with AF-liposomes, and also increased gene transfer activity as the entrapment ratio of pDNA into AF-liposomes was increased. γ-CyD stabilized the liposomal membrane of AF-liposomes and inhibited the release of calcein from AF-liposomes. The stabilizing effect of γ-CyD may be, at least in part, involved in the enhancing gene transfer activity of pDNA/γ-CyD/AF-liposomes. Therefore, these results suggest the potential use of γ-CyD for an enhancer of transfection efficiency of AF-liposomes.
本研究的目的是评估以脱唾液酸胎球蛋白附加阳离子脂质体(AF-脂质体)与环糊精结合(CyD/AF-脂质体)作为肝细胞选择性非病毒载体介导的体外基因传递。在各种环糊精中,与质粒DNA(pDNA)和γ-环糊精(γ-CyD)结合的AF-脂质体(pDNA/γ-CyD/AF-脂质体)在HepG2细胞中显示出最高的基因转移活性,且无明显细胞毒性。此外,γ-CyD提高了pDNA与AF-脂质体的包封率,并且随着pDNA包封到AF-脂质体中的包封率增加,基因转移活性也增强。γ-CyD稳定了AF-脂质体的脂质体膜,并抑制了钙黄绿素从AF-脂质体中的释放。γ-CyD的稳定作用可能至少部分地参与了pDNA/γ-CyD/AF-脂质体增强基因转移活性的过程。因此,这些结果表明γ-CyD有可能用作提高AF-脂质体转染效率的增强剂。