Paclitaxel-loaded PEGylated nanocapsules of perfluorooctyl bromide as theranostic agents

被引:32
作者
Boissenot, Tanguy [1 ]
Fattal, Elias [1 ]
Bordat, Alexandre [1 ]
Houvenagel, Sophie [1 ]
Valette, Julien [2 ]
Chacun, Helene [1 ]
Gueutin, Claire [1 ]
Tsapis, Nicolas [1 ]
机构
[1] Univ Paris Saclay, Univ Paris Sud, CNRS, Inst Galien Paris Sud, 5 Rue JB Clement, F-92296 Chatenay Malabry, France
[2] Mol Imaging Res Ctr MIRCen, Inst Imagerie Biomed I2BM, Commissariat Energie Atom CEA, Fontenay Aux Roses, France
关键词
Paclitaxel; Theranostics; Nanocapsules; F-19-MRI; PLGA-BASED NANOPARTICLES; F-19; MAGNETIC-RESONANCE; DRUG-DELIVERY SYSTEM; IN-VIVO; TUMOR; MORPHOLOGY; VITRO; MR; PERMEABILITY; FLUORESCENT;
D O I
10.1016/j.ejpb.2016.08.017
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
We optimize the encapsulation of paclitaxel (PTX) into nanocapsules made of a shell of poly(lactide-co-glycolide)-polyethylene glycol and a core of perfluorooctyl bromide (PFOB) to serve as theranostic agents. Two main challenges were met: keeping the imaging moiety (PFOB) encapsulated while loading the polymer shell with a hydrophobic drug very prone to crystallization. Encapsulation is performed by a modified emulsion-evaporation method leading to 120 nm diameter nanocapsules with a drug loading compatible with tumor treatment. The optimized formulation tested in vitro on CT-26 colon cancer cells yields a similar IC50 as the generic Taxol (R) formulation. In vivo, F-19-MRI shows that PTX encapsulation does not modify the ability of nanocapsules to accumulate passively in CT-26 tumors in mice by the enhanced permeation and retention (EPR) effect. This accumulation leads to a promising and statistically significant twofold reduction in tumor growth as compared with negative control and generic Taxol group. Altogether these results advocate for an interesting potential of these paclitaxel-loaded theranostic agents. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:136 / 144
页数:9
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