Highly efficient siRNA delivery system into human and murine cells using single-wall carbon nanotubes

被引:67
作者
Ladeira, M. S. [1 ]
Andrade, V. A. [1 ]
Gomes, E. R. M. [1 ]
Aguiar, C. J. [1 ]
Moraes, E. R. [1 ]
Soares, J. S. [2 ]
Silva, E. E. [2 ]
Lacerda, R. G. [2 ]
Ladeira, L. O. [2 ]
Jorio, A. [2 ]
Lima, P. [3 ]
Leite, M. Fatima [1 ,4 ]
Resende, R. R. [2 ,5 ]
Guatimosim, S. [1 ]
机构
[1] Univ Fed Minas Gerais, Dept Physiol & Biophys, BR-31270901 Belo Horizonte, MG, Brazil
[2] Univ Fed Minas Gerais, Dept Phys, BR-31270901 Belo Horizonte, MG, Brazil
[3] Univ Fed Sao Joao del Rei, Dept Biosyst Engn, BR-36307352 Sao Joao Del Rei, MG, Brazil
[4] Howard Hughes Med Inst, Chevy Chase, MD 20815 USA
[5] Univ Fed Sao Joao del Rei, Dept Biochem, Adv Ctr Hlth, BR-35501296 Divinopolis, MG, Brazil
关键词
INOSITOL 1,4,5-TRISPHOSPHATE RECEPTOR; NEAR-INFRARED FLUORESCENCE; SMALL INTERFERING RNA; INTRACELLULAR DELIVERY; MAMMALIAN-CELLS; IN-VITRO; CALCIUM; FUNCTIONALIZATION; RETICULUM; SIGNALS;
D O I
10.1088/0957-4484/21/38/385101
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Development of RNA interference (RNAi) technology utilizing short interfering RNA sequences (siRNA) has focused on creating methods for delivering siRNAs to cells and for enhancing siRNA stability in vitro and in vivo. Here, we describe a novel approach for siRNA cellular delivery using siRNA coiling into carboxyl-functionalized single-wall carbon nanotubes (SWCNTs). The CNT-siRNA delivery system successfully demonstrates nonspecific toxicity and transfection efficiency greater than 95%. This approach offers the potential for siRNA delivery into different types of cells, including hard-to-transfect cells, such as neuronal cells and cardiomyocytes. We also tested the CNT-siRNA system in a non-metastatic human hepatocellular carcinoma cell line (SKHep1). In all types of cells used in this work the CNT-siRNA delivery system showed high efficiency and apparent no side effects for various in vitro applications.
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页数:12
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