Dual anticancer drug/superparamagnetic iron oxide-loaded PLGA-based nanoparticles for cancer therapy and magnetic resonance imaging

被引:177
作者
Schleich, N. [1 ]
Sibret, P. [2 ]
Danhier, P. [3 ]
Ucakar, B. [1 ]
Laurent, S. [4 ]
Muller, R. N. [4 ,5 ]
Jerome, C. [2 ]
Gallez, B. [3 ]
Preat, V. [1 ]
Danhier, F. [1 ]
机构
[1] Catholic Univ Louvain, Louvain Drug Res Inst, B-1200 Brussels, Belgium
[2] Univ Liege, Ctr Educ & Res Macromol, B-4000 Liege, Belgium
[3] Catholic Univ Louvain, Louvain Drug Res Inst, Lab Biomed Magnet Resonance, B-1200 Brussels, Belgium
[4] Univ Mons, Dept Gen Organ & Biomed Chem, NMR & Mol Imaging Lab, B-7000 Mons, Belgium
[5] CMMI, B-6041 Gosselies, Belgium
关键词
PLGA-nanoparticles; SPIO; Paclitaxel; Cancer therapy; Magnetic resonance imaging; DRUG-DELIVERY; SUPERPARAMAGNETIC NANOPARTICLES; IN-VITRO; M-CELLS; MRI; PACLITAXEL; NANOMEDICINE; RELAXATION; MICELLES;
D O I
10.1016/j.ijpharm.2013.02.042
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
We developed dual paclitaxel (PTX)/superparamagnetic iron oxide (SPIO)-loaded PLGA-based nanoparticles for a theranostic purpose. Nanoparticles presented a spherical morphology and a size of 240 nm. The PTX and iron loading were 1.84 +/- 0.4 and 10.4 +/- 1.93 mg/100 mg respectively. Relaxometry studies and phantom MRI demonstrated their efficacy as T-2 contrast agent. Significant cellular uptake by CT26 cells of nanoparticles was shown by Prussian blue staining and fluorescent microscopy. While SPIO did not show any toxicity in CT-26 cells, PTX-loaded nanoparticles had a cytotoxic activity. PTX-loaded nanoparticle (5 mg/kg) with or without co-encapulated SPIO induced in vivo a regrowth delay of CT26 tumors. Together these multifunctional nanoparticles may be considered as future nanomedicine for simultaneous molecular imaging, drug delivery and real-time monitoring of therapeutic response. (C) 2013 Elsevier B. V. All rights reserved.
引用
收藏
页码:94 / 101
页数:8
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