Electrostatic assembly of a DNA superparamagnetic nano-tool for simultaneous intracellular delivery and in situ monitoring

被引:28
作者
Geinguenaud, Frederic [1 ]
Souissi, Ines [2 ]
Fagard, Remi [2 ,3 ]
Motte, Laurence [1 ]
Lalatonne, Yoann [1 ,4 ]
机构
[1] Univ Paris 13, UMR CNRS 7244, Lab CSPBAT, Bobigny, France
[2] Univ Paris 13, INSERM U978, Bobigny, France
[3] Hop Avicenne, APHP, Serv Biochim, F-93009 Bobigny, France
[4] Hop Avicenne, APHP, Nucl Med Serv, F-93009 Bobigny, France
关键词
DNA; Decoy ODN; Delivery nanosystem; Nanoprobes; Superparamagnetic nanoparticle; IRON-OXIDE NANOPARTICLES; GENE DELIVERY; MAGNETIC NANOPARTICLES; SIGNAL TRANSDUCER; GOLD NANOPARTICLES; NUCLEIC-ACIDS; VIVO; HYBRIDIZATION; RESONANCE; ACTIVATOR;
D O I
10.1016/j.nano.2011.12.010
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
A superparamagnetic gamma Fe2O3 nanocarrier was developed, characterized by spectroscopic methods and evaluated for the delivery of a decoy oligonucleotide (dODN) in human colon carcinoma SW 480 cells. This nanoparticle-dODN bioconjugate (gamma Fe2O3@dODN) was designed to target the signal transducer and activator of transcription 3, STAT3, a key regulator of cell survival and proliferation. We exploited a simple precipitation-redispersion mechanism for the direct and one-step complexation of a labeled decoy oligonucleotide with iron oxide nanoparticles (NPs). The cell internalization of the decoy gamma Fe2O3@dODN nanoparticles is demonstrated and suggests the potential for DNA delivery in biological applications. Despite the increasing use of NPs in biology and medicine, convenient methods to quantify them within cells are still lacking. In this work, taking advantage of the nonlinear magnetic behavior of our superparamagnetic NPs, we have developed a new method to quantify in situ their internalization by cells. From the Clinical Editor: In this study, the authors demonstrate methods to quantify superparamagnetic nanocarriers within cells, taking advantage of the nonlinear magnetic behavior of the studied NPs. (C) 2012 Published by Elsevier Inc.
引用
收藏
页码:1106 / 1115
页数:10
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