Enhanced cellular internalization and gene silencing with a series of cationic dendron‐multiwalled carbon nanotube:siRNA complexes
Models, Molecular
570
MESH: Cell Line, Tumor
Nonviral
Cell Survival
MESH: Biological Transport
610
Research Support
Small Interfering
Transfection
01 natural sciences
Cell Line
[SDV.SP.MED]Life Sciences [q-bio]/Pharmaceutical sciences/Medication
Models
Cations
Cell Line, Tumor
MESH: RNA, Small Interfering
Journal Article
Nanotechnology
Humans
MESH: Gene Silencing
Gene Silencing
RNA, Small Interfering
Non-U.S. Gov't
MESH: Cations
Gene transfer
Tumor
Nanotubes
MESH: Humans
carbon nanotubes
Nanotubes, Carbon
MESH: Transfection
Molecular
Biological Transport
540
Carbon
MESH: Cell Line
0104 chemical sciences
MESH: Hela Cells
MESH: Cell Survival
MESH: Nanotubes, Carbon
RNA
Knockdown
Interference
MESH: Models, Molecular
HeLa Cells
DOI:
10.1096/fj.09-141036
Publication Date:
2010-07-21T04:07:45Z
AUTHORS (12)
ABSTRACT
One of the major obstacles to the clinical development of gene silencing by small interfering RNA (siRNA) is its effective cytoplasmic delivery. Carbon nanotubes have been proposed as novel nanomaterials that can offer significant advantages for the intracellular delivery of nucleic acids, such as siRNA. We recently demonstrated in a proof-of-principle study that amino-functionalized multiwalled carbon nanotubes (f-MWNT) can effectively deliver in vivo an siRNA sequence, triggering cell apoptosis that results in human lung xenograft eradication and prolonged survival. In the present study, we demonstrate how a newly synthesized series of polycationic dendron-MWNT constructs with a precisely tailored number of amino functions (dendron generations) can complex and effectively deliver double-stranded siRNA to achieve gene silencing in vitro. A systematic comparison between the f-MWNT series in terms of cellular uptake, cytotoxicity, and siRNA complexation is offered. Significant improvement in siRNA delivery with the dendron-MWNT conjugates is shown, and gene silencing was obtained in 2 human cell lines using 2 different siRNA sequences. The study reveals that through f-MWNT structure-biological function analysis novel nanotube-based siRNA transfer vectors can be designed with minimal cytotoxicity and effective delivery and gene-silencing capabilities.
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CITATIONS (63)
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