Influence of surfactants, polymer and doxorubicin loading on the anti-tumour effect of poly(butyl cyanoacrylate) nanoparticles in a rat glioma model

被引:90
作者
Ambruosi, Alessandra
Gelperina, Svetlana
Khalansky, Alexander
Tanski, Sandra
Theisen, Alf
Kreuter, Joerg
机构
[1] Goethe Univ Frankfurt, Inst Pharmaceut Technol, D-60439 Frankfurt, Germany
[2] Res Ctr Mol Diagnost & Therapy, Moscow, Russia
[3] Russian Acad Med Sci, Inst Human Morphol, Moscow, Russia
[4] Goethe Univ Frankfurt, Zent Forsch Anstalt, D-6000 Frankfurt, Germany
关键词
nanoparticles; glioblastomas; brain tumours; rats; poly(n-butyl cyanoacrylate); poly(iso-butyl cyanoacrylate); doxorubicin; polysorbate; 80; poloxamine; 908; poloxamer; 188;
D O I
10.1080/02652040600788080
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Poly(n-butyl cyanoacrylate) nanoparticles coated with polysorbate-80 can enable the transport of bound drugs across the blood - brain barrier (BBB) after i.v. injection. In the present study the influence of different formulation parameters on the anti-tumoural effects of doxorubicin nanoparticles against glioblastoma 101/8 was investigated. The manufacturing parameters of poly(alkyl cyanoacrylate) doxorubicin-loaded nanoparticles were optimized concerning drug loading. The nanoparticles were coated with different surfactants and injected intravenously on days 2, 5 and 8 after intra-cranial implantation of glioblastoma 101/8 to rats. The survival times of all doxorubicin containing preparations, including a doxorubicin solution, increased the survival times significantly compared to untreated tumour- bearing rats. The most pronounced increase in survival was obtained with the poly(n-butyl cyanoacrylate) doxorubicin-loaded nanoparticles coated with polysorbate 80 and 35% of these animals survived for over 180 days (termination of the experiments). The other nanoparticle preparations yielded lower survival times. Poly(n-butyl cyanoacrylate) doxorubicin-loaded nanoparticles coated with polysorbate 80-coated proved to be very efficient against glioblastoma 101/8. The data suggest that the interaction of nanoparticles with the blood after injection as well as the enhanced permeability and retention effect (EPR effect) contributed differently to the anti-tumoural efficacy depending on nanoparticle formulation and surface properties.
引用
收藏
页码:582 / 592
页数:11
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