Kawakami Shigeru, Harada Ayaka, Sakanaka Koji, Nishida Koyo, Nakamura Junzo, Sakaeda Toshiyuki, Ichikawa Nobuhiro, Nakashima Mikiro, Sasaki Hitoshi
Graduate School of Biomedical Sciences, Nagasaki University, 1-14 Bunkyo-machi, 852-8521, Japan.
Int J Pharm. 2004 Jul 8;278(2):255-62. doi: 10.1016/j.ijpharm.2004.03.013.
To optimize the in vivo ocular transfection efficiency of plasmid DNA (pDNA)/cationic liposome complexes, N-[1-(2,3-dioleyloxy)propyl]-N,N,N-trimethylammonium chloride (DOTMA)/dioleoylphosphatidylethanolamine (DOPE) (1:1 molar ratio) liposomes and DOTMA/cholesterol (Chol) (1:1 molar ratio) liposomes were prepared with varying amounts of pDNA. pDNA/cationic liposome complexes were intravitreally injected (100 microL) in rabbits, and luciferase activity in the cornea, aqueous humor, iris-ciliary body, lens, vitreous body, and retina was measured. Transfection efficiency of pDNA alone did not change with pDNA ranging from 40 to 85 mg. In contrast, transfection efficiency of pDNA complexed with DOTMA/Chol liposomes significantly increased with the amount of pDNA ranging from 40 to 85 microg (P < 0.05). pDNA complexed with DOTMA/DOPE liposomes could not be prepared with pDNA greater than 60 microg. Among these experiments, pDNA (85 microg) complexed with DOTMA/Chol liposomes (pDNA:cationic liposome charge ratio (- : +) = 1.0:2.0) showed the highest transfection efficiency in the ocular tissue and its transfection-mediated luciferase activity peaked at 3 days. Among the ocular tissues, the highest gene expression was observed in the aqueous humor.
为优化质粒DNA(pDNA)/阳离子脂质体复合物的体内眼内转染效率,制备了不同量pDNA的N-[1-(2,3-二油酰氧基)丙基]-N,N,N-三甲基氯化铵(DOTMA)/二油酰磷脂酰乙醇胺(DOPE)(摩尔比1:1)脂质体和DOTMA/胆固醇(Chol)(摩尔比1:1)脂质体。将pDNA/阳离子脂质体复合物玻璃体内注射(100微升)到兔体内,然后测量角膜、房水、虹膜睫状体、晶状体、玻璃体和视网膜中的荧光素酶活性。单独的pDNA转染效率在pDNA量为40至85微克时没有变化。相比之下,与DOTMA/Chol脂质体复合的pDNA转染效率随着pDNA量从40至85微克显著增加(P<0.05)。与DOTMA/DOPE脂质体复合的pDNA在pDNA大于60微克时无法制备。在这些实验中,与DOTMA/Chol脂质体复合的pDNA(85微克)(pDNA:阳离子脂质体电荷比(- : +)=1.0:2.0)在眼组织中显示出最高的转染效率,其转染介导的荧光素酶活性在第3天达到峰值。在眼组织中,房水中观察到最高的基因表达。