Cell targeting by a generic receptor-targeted polymer nanocontainer platform

被引:171
作者
Broz, P
Benito, SM
Saw, C
Burger, P
Heider, H
Pfisterer, M
Marsch, S
Meier, W
Hunziker, P
机构
[1] Univ Basel Hosp, Med Intens Care Unit, CH-4031 Basel, Switzerland
[2] Univ Basel, Dept Chem, CH-4056 Basel, Switzerland
[3] Univ Basel, Natl Ctr Competence Res Nanoscale Sci, CH-4056 Basel, Switzerland
[4] Univ Basel, Inst Biochem & Genet, CH-4051 Basel, Switzerland
[5] Univ Basel Hosp, Dept Cardiol, CH-4031 Basel, Switzerland
关键词
polymer nanocontainer; receptor targeting; macrophage scavenger receptor Al; drug delivery;
D O I
10.1016/j.jconrel.2004.10.014
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Nanotechnology promises new avenues to medical diagnosis and treatment. Of special interest are injectable nanovehicles that are programmable towards specific targets, are able to evade the immune defense, and are versatile enough to be suited as carriers of complex functionality. Biotin-functionalized (poly(2-methyloxazoline)-b-poly(dimethylsiloxane)-b-poly(2-methyloxazoline) triblock copolymers were self-assembled to form nanocontainers, and biotinylated targeting ligands were attached by using streptavidin as a coupling agent. Specifically, fluorescence-labeled nanocontainers were targeted against the scavenger receptor Al from macrophages, an important cell in human disease. In human and transgenic cell lines and in mixed cultures, receptor-specific binding of these generic carriers was followed by vesicular uptake. Low nonspecific binding supported the "stealth" properties of the carrier while cytotoxicity was absent. This versatile carrier appears promising for diagnostic or therapeutic medical use. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:475 / 488
页数:14
相关论文
共 47 条
[1]   Medical progress: Chronic obstructive pulmonary disease. [J].
Barnes, PJ .
NEW ENGLAND JOURNAL OF MEDICINE, 2000, 343 (04) :269-280
[2]   HIGHER-ORDER SELF-ASSEMBLY OF VESICLES BY SITE-SPECIFIC BINDING [J].
CHIRUVOLU, S ;
WALKER, S ;
ISRAELACHVILI, J ;
SCHMITT, FJ ;
LECKBAND, D ;
ZASADZINSKI, JA .
SCIENCE, 1994, 264 (5166) :1753-1756
[3]   Advances in immunology - Autoimmune diseases [J].
Davidson, A ;
Diamond, B .
NEW ENGLAND JOURNAL OF MEDICINE, 2001, 345 (05) :340-350
[4]   Polymersomes: Tough vesicles made from diblock copolymers [J].
Discher, BM ;
Won, YY ;
Ege, DS ;
Lee, JCM ;
Bates, FS ;
Discher, DE ;
Hammer, DA .
SCIENCE, 1999, 284 (5417) :1143-1146
[5]   Viruses in therapy - royal road or dead end? [J].
Dobbelstein, M .
VIRUS RESEARCH, 2003, 92 (02) :219-221
[6]   Anticancer drug delivery with transferrin targeted polymeric chitosan vesicles [J].
Dufes, C ;
Muller, JM ;
Couet, W ;
Olivier, JC ;
Uchegbu, IF ;
Schätzlein, AG .
PHARMACEUTICAL RESEARCH, 2004, 21 (01) :101-107
[7]  
DUNN WA, 1980, J BIOL CHEM, V255, P5971
[8]   Ligand-specific targeting of microspheres to phagocytes by surface modification with poly(L-lysine)-grafted poly(ethylene glycol) conjugate [J].
Faraasen, S ;
Vörös, J ;
Csúcs, G ;
Textor, M ;
Merkle, HP ;
Walter, E .
PHARMACEUTICAL RESEARCH, 2003, 20 (02) :237-246
[9]   The role of the macrophage in apoptosis: Hunter, gatherer, and regulator [J].
Geske, FJ ;
Monks, J ;
Lehman, L ;
Fadok, VA .
INTERNATIONAL JOURNAL OF HEMATOLOGY, 2002, 76 (01) :16-26
[10]   Virus-assisted loading of polymer nanocontainer [J].
Graff, A ;
Sauer, M ;
Van Gelder, P ;
Meier, W .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (08) :5064-5068