| Literature DB >> 24694458 |
Takahiro Nomoto1, Shigeto Fukushima2, Michiaki Kumagai2, Kaori Machitani2, Yu Matsumoto3, Makoto Oba4, Kanjiro Miyata3, Kensuke Osada5, Nobuhiro Nishiyama6, Kazunori Kataoka7.
Abstract
Nanocarriers responding to light have great potential for pinpoint therapy, and recent studies have revealed promising in vivo activity. However, light-selective gene transfer still remains challenging in the systemic application. Here we report systemic light-responsive nanocarriers for gene delivery developed through the sequential self-assembly of ABC-type triblock copolymer/DNA/dendrimeric photosensitizer, forming polyplex micelles with three-layered functional nanocompartments. The DNA-packaged core is covered by the photosensitizer-incorporated intermediate layer, which is encompassed by an outer shielding shell. This three-layered structure permits multistep photosensitizer and DNA delivery into a solid tumour by a systemic route: the shielding layer minimizes unfavourable interactions with blood components, and the photosensitizer is delivered to endo-/lysosomal membranes to facilitate light-selective cytoplasmic translocation of the micelles, accomplishing DNA delivery into the nucleus to exert gene expression. The polyplex micelles display >100-fold photoenhanced gene expression in cultured cells and exhibit light-induced in vivo gene transfer in solid tumours following systemic administration.Entities:
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Year: 2014 PMID: 24694458 DOI: 10.1038/ncomms4545
Source DB: PubMed Journal: Nat Commun ISSN: 2041-1723 Impact factor: 14.919