The effect of functionalizing lipid nanocapsules with NFL-TBS.40-63 peptide on their uptake by glioblastoma cells

被引:58
作者
Balzeau, Julien [1 ]
Pinier, Maud [1 ]
Berges, Raphael [1 ]
Saulnier, Patrick [2 ]
Benoit, Jean-Pierre [2 ]
Eyer, Joel [1 ]
机构
[1] CHU Angers, Lab Neurobiol & Transgenese, UPRES EA3143, LUNAM, F-49033 Angers, France
[2] CHU Angers, Micro & Nanomed Therapeut MINT, UMR INSERM 1066, F-49033 Angers, France
关键词
Glioblastoma; Lipid nanocapsules; NFL-TBS.40-63; peptide; Paclitaxel; MALIGNANT GLIOMA; TUBULIN; LIPOSOMES;
D O I
10.1016/j.biomaterials.2013.01.068
中图分类号
R318 [生物医学工程];
学科分类号
100103 [病原生物学];
摘要
We previously described a neurofilament derived cell-penetrating peptide, NFL-TBS.40-63, that specifically enters in glioblastoma cells where it disturbs the microtubule network both in vitro and in vivo. The aim of this study is to test whether this peptide can increase the targeted uptake by glioblastoma cells of lipid nanocapsules filled with Paclitaxel, and thus can increase their anti-proliferation in vitro and in vivo. Here, using the drop tensiometry we show that approximately 60 NFL-TBS.40-63 peptides can bind to one 50 nm lipid nanocapsule. When nanocapsules are filled with a far-red fluorochrome (DiD) and Paclitaxel, the presence of the NFL-TBS.40-63 peptide increases their uptake by glioblastoma cells in culture as evaluated by FACS analysis, and thus reduces their proliferation. Finally, when such nanocapsules were injected in mice bearing a glioma tumour, they are preferentially targeted to the tumour and reduce its progression. These results show that nanocapsules functionalized with the NFL-TBS.40-63 peptide represent a powerful drug-carrier system for glioma targeted treatment. (C) 2013 Elsevier Ltd. All rights reserved.
引用
收藏
页码:3381 / 3389
页数:9
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