作者: Xia Li , Hui Guo , Junliang Wang , Qi Wu , Xianfu Lin
DOI: 10.1016/J.ACTBIO.2009.07.002
关键词:
摘要: Novel hepatoma-targeting azacitidine-conjugating microdisks were successfully fabricated by hydrogen bond-assisted self-assembly of an amphiphilic random copolymer with galactose and azacitidine as pendants, poly(5'-O-vinyladipyl-azacitidine-co-6-O-vinylsebacyl-galactose). The was easily prepared a two-step chemoenzymatic synthetic route, the possibility its verified ultraviolet-visible fluorescence spectroscopy using pyrene hydrophobic probe. Transmission electron microscopy scanning indicated that aggregation morphologies these self-assemblies thin disks radii from 250 to 500nm. Section analysis atomic force for disk gave thickness approximately 16nm. existence bonds among pendants investigated infrared spectra Gaussian calculation. Cellular uptake assay observed confocal laser cell cytotoxicity tests MTT dye reduction method showed had evident function hepG2 human hepatoma cells could effectively realize cellular internalization azacitidine.