Delivery of nanoparticles to the brain detected by fluorescence microscopy

被引:77
作者
Reimold, Isolde [1 ]
Domke, Diana [2 ]
Bender, Joe [2 ]
Seyfried, Christoph A. [2 ]
Radunz, Hans-Eckhard [2 ]
Fricker, Gert [1 ]
机构
[1] Heidelberg Univ, Inst Pharm & Mol Biotechnol, D-69120 Heidelberg, Germany
[2] NanoDel Technol GmbH, Magdeburg, Germany
关键词
Poly(n-butylcyano-acrylate) (PBCA) nanoparticles; Blood-brain barrier; Drug delivery;
D O I
10.1016/j.ejpb.2008.05.007
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
This study aimed to explore and extend the application potential of poly(n-butylcyano-acrylate) (PBCA) nanoparticles to cross the blood-brain barrier (BBB) and to deliver their content into the central nervous system. PBCA particles were prepared by a new and efficient mini-emulsion method with excellent yield and reproducibility. These nanoparticles were loaded with 1.5% (w/v) fluorescein-isothio-cyanate-dextran (FITC-dextran), 1.5% rhodamine-123 or 7.3% doxorubicin. Particles were characterized by dynamic light scattering determining particle size, polydispersity index and zeta-potential. They were coated with 10% w/v polysorbate 80 and administered to rats. Cryosections of the brain were prepared and time-dependent distribution Of fluorescence was studied. After the administration of polysorbate 80-coated particles by carotic injection, fluorescence could first be detected in capillary lumina with a progressive shift to capillary endothelial cells at 30 min and a rather evenly spread distribution across the brain tissue at 60 min after administration. 60 min after administration into the tail vein, fluorescent particles could be assigned to endothelial cells, whereas after 2 h a rather evenly spread distribution across the brain tissue was seen. These observations indicate that surface-coated PBCA nanoparticles are able to cross the blood-brain barrier and to serve as a drug-delivery, system to the central nervous system. (C) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:627 / 632
页数:6
相关论文
共 18 条
[1]   Influence of surfactants, polymer and doxorubicin loading on the anti-tumour effect of poly(butyl cyanoacrylate) nanoparticles in a rat glioma model [J].
Ambruosi, Alessandra ;
Gelperina, Svetlana ;
Khalansky, Alexander ;
Tanski, Sandra ;
Theisen, Alf ;
Kreuter, Joerg .
JOURNAL OF MICROENCAPSULATION, 2006, 23 (05) :582-592
[2]  
Bauer B, 2005, EXP BIOL MED, V230, P118
[3]   In vitro and in vivo evaluations of dihydroquinoline- and dihydroisoquinoline-based targetor moieties for brain-specific chemical delivery systems [J].
Bodor, N ;
Farag, HH ;
Barros, MDC ;
Wu, WM ;
Buchwald, P .
JOURNAL OF DRUG TARGETING, 2002, 10 (01) :63-71
[4]   The role of plasma proteins in brain targeting:: species dependent protein adsorption patterns on brain-specific lipid drug conjugate (LDC) nanoparticles [J].
Gessner, A ;
Olbrich, C ;
Schröder, W ;
Kayser, O ;
Müller, RH .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2001, 214 (1-2) :87-91
[5]   Role of drug efflux carriers in the healthy and diseased brain [J].
Hermann, Dirk M. ;
Kilic, Ertugrul ;
Spudich, Annett ;
Kraemer, Stefanie D. ;
Wunderli-Allenspach, Heidi ;
Bassetti, Claudio L. .
ANNALS OF NEUROLOGY, 2006, 60 (05) :489-498
[6]   Paclitaxel nanoparticles for the potential treatment of brain tumors [J].
Koziara, JM ;
Lockman, PR ;
Allen, DD ;
Mumper, RJ .
JOURNAL OF CONTROLLED RELEASE, 2004, 99 (02) :259-269
[7]  
Kozler P, 2003, Sb Lek, V104, P255
[8]   Apolipoprotein-mediated transport of nanoparticle-bound drugs across the blood-brain barrier [J].
Kreuter, J ;
Shamenkov, D ;
Petrov, V ;
Ramge, P ;
Cychutek, K ;
Koch-Brandt, C ;
Alyautdin, R .
JOURNAL OF DRUG TARGETING, 2002, 10 (04) :317-325
[9]   Covalent attachment of apolipoprotein A-I and apolipoprotein B-100 to albumin nanoparticles enables drug transport into the brain [J].
Kreuter, Jorg ;
Hekmatara, Telli ;
Dreis, Sebastian ;
Vogel, Tikva ;
Gelperina, Svetlana ;
Langer, Klaus .
JOURNAL OF CONTROLLED RELEASE, 2007, 118 (01) :54-58
[10]   The use of surfactants to enhance the permeability of peptides through Caco-2 cells by inhibition of an apically polarized efflux system [J].
Nerurkar, MM ;
Burton, PS ;
Borchardt, RT .
PHARMACEUTICAL RESEARCH, 1996, 13 (04) :528-534