In vitro antitumor activity of methotrexate via pH-sensitive chitosan nanoparticles

被引:161
|
作者
Rubert Nogueira, Daniele [1 ]
Tavano, Lorena [2 ,3 ,4 ]
Mitjans, Montserrat [1 ,5 ]
Perez, Lourdes [2 ]
Rosa Infante, M. [2 ]
Pilar Vinardell, M. [1 ,5 ]
机构
[1] Univ Barcelona, Fac Farm, Dept Fisiol, E-08028 Barcelona, Spain
[2] CSIC, IQAC, Dept Tecnol Quim & Tensioact, ES-08034 Barcelona, Spain
[3] Univ Calabria, Dept Pharmaceut Sci, I-87036 Cosenza, Italy
[4] Univ Calabria, Dept Modeling Engn, I-87036 Cosenza, Italy
[5] CSIC, Unidad Asociada, Barcelona, Spain
关键词
Chitosan nanoparticles; Methotrexate; Lysine-based surfactant; Intracellular drug delivery; pH-sensitivity; Cytotoxicity; LYSINE-BASED SURFACTANTS; DIHYDROFOLATE-REDUCTASE; TPP NANOPARTICLES; LOADED CHITOSAN; GLYCOL CHITOSAN; CANCER-THERAPY; PARTICLE-SIZE; CYTOTOXICITY; DELIVERY; MEMBRANE;
D O I
10.1016/j.biomaterials.2013.01.005
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Nanoparticles with pH-sensitive behavior may enhance the success of chemotherapy in many cancers by efficient intracellular drug delivery. Here, we investigated the effect of a bioactive surfactant with pH-sensitive properties on the antitumor activity and intracellular behavior of methotrexate-loaded chitosan nanoparticles (MTX-CS-NPs). NPs were prepared using a modified ionotropic complexation process, in which was included the surfactant derived from N-alpha,N-epsilon-dioctanoyl lysine with an inorganic lithium counterion. The pH-sensitive behavior of NPs allowed accelerated release of MTX in an acidic medium, as well as membrane-lytic pH-dependent activity, which facilitated the cytosolic delivery of endocytosed materials. Moreover, our results clearly proved that MTX-CS-NPs were more active against the tumor HeLa and MCF-7 cell lines than the free drug. The feasibilty of using NPs to target acidic tumor extracellular pH was also shown, as cytotoxicity against cancer cells was greater in a mildly acidic environment. Finally, the combined physicochemical and pH-sensitive properties of NPs generally allowed the entrapped drug to induce greater cell cycle arrest and apoptotic effects. Therefore, our overall results suggest that pH-sensitive MTX-CS-NPs could be potentially useful as a carrier system for tumor and intracellular drug delivery in cancer therapy. (c) 2013 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2758 / 2772
页数:15
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