| Literature DB >> 24384299 |
Tomoaki Kurosaki1, Shigeru Kawakami2, Yuriko Higuchi3, Ryo Suzuki4, Kazuo Maruyama4, Hitoshi Sasaki5, Fumiyoshi Yamashita3, Mitsuru Hashida6.
Abstract
Anionic bubble lipopolyplexes have been developed as anionic ultrasound (US)-responsive gene delivery carriers with biocompatible compounds for efficient and safe transfection in mice. The particles of the anionic bubble lipopolyplexes were approximately 450-600nm with an anionic surface charge. In the absence of US exposure, the bubble lipopolyplexes showed extremely low gene expression in the human vascular endothelial cell line EAhy926. The anionic bubble lipopolyplexes, however, delivered pDNA into cells without endocytosis and showed markedly high gene expression following US exposure. The anionic bubble lipopolyplexes showed little cytotoxicity in EAhy926 cells and little aggregation with erythrocytes. Following intravenous administration into mice, the anionic bubble lipopolyplexes showed high levels of gene expression in the liver, kidney, and spleen only after US exposure to the abdominal area. The level of gene expression in liver non-parenchymal cells was significantly higher than that in parenchymal cells. In addition, the anionic bubble lipopolyplexes did not show any severe hepatic toxicity and did not enhance the production of proinflammatory cytokines. Overall, we have succeeded in preparing anionic bubble lipopolyplexes for efficient and safe transfection with US exposure in mice.Entities:
Keywords: Biocompatibility; DNA; Liposomes; Self assembly; Sonoporation; Transfection
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Year: 2013 PMID: 24384299 DOI: 10.1016/j.jconrel.2013.12.023
Source DB: PubMed Journal: J Control Release ISSN: 0168-3659 Impact factor: 9.776