Novel Guanidine-Containing Molecular Transporters Based on Lactose Scaffolds: Lipophilicity Effect on the Intracellular Organellar Selectivity

被引:25
作者
Biswas, Goutam [1 ]
Jeon, Ock-Youm [1 ]
Lee, Woo Sirl [1 ]
Kim, Dong-Chan [2 ]
Kim, Kyong-Tai [2 ]
Lee, Suho [3 ]
Chang, Sunghoe [3 ]
Chung, Sung-Kee [1 ]
机构
[1] Pohang Univ Sci & Technol, Dept Chem, Pohang 790784, South Korea
[2] Pohang Univ Sci & Technol, Dept Life Sci, Pohang 790784, South Korea
[3] Gwangju Inst Sci & Technol, Dept Life Sci, Kwangju 500712, South Korea
关键词
blood-brain barrier; drug delivery; lipophilicity; organelle selectivity; tissue selectivity;
D O I
10.1002/chem.200801160
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We have synthesized two lactose-based molecular transporters, each containing seven guanidine residues attached to the lactose scaffold through omega-aminocarboxylate linker chains of two different lengths, and have examined their cellular uptakes and intracellular and organellar localizations in HeLa cells, as well as their tissue distributions in mice. Both molecular transporters showed higher cellular uptake efficiencies than Arg8, and wide tissue distributions including the brain. Mitochondrial localization is of special interest because of its potential relevance to "mitochondrial diseases". Interestingly, it has been found that the intracellular localization sites of the G7 molecular transporters-namely either mitochondria or lysosomes and endocytic vesicles-are largely determined by the linker chain lengths, or their associated lipophilicities.
引用
收藏
页码:9161 / 9168
页数:8
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