Synthesis and characterization of core-shell star copolymers for in vivo PET imaging applications

被引:131
作者
Fukukawa, Ken-ichi [1 ,2 ,3 ]
Rossin, Raffaella
Hagooly, Aviv
Pressly, Eric D. [1 ,2 ,3 ]
Hunt, Jasmine N. [1 ,2 ,3 ]
Messmore, Benjamin W. [1 ,2 ,3 ]
Wooley, Karen L.
Welch, Michael J.
Hawker, Craig J. [1 ,2 ,3 ]
机构
[1] Univ Calif Santa Barbara, Mat Res Lab, Dept Chem, Santa Barbara, CA 93106 USA
[2] Univ Calif Santa Barbara, Mat Res Lab, Dept Biochem, Santa Barbara, CA 93106 USA
[3] Univ Calif Santa Barbara, Mat Res Lab, Dept Mat, Santa Barbara, CA 93106 USA
关键词
D O I
10.1021/bm7014152
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The synthesis of core-shell star copolymers via living free radical polymerization provides a convenient route to three-dimensional nanostructures having a poly(ethylene glycol) outer shell, a hydrophilic inner shell bearing reactive functional groups, and a central hydrophobic core. By starting with well-defined linear diblock copolymers, the thickness of each layer, overall size/molecular weight, and the number of internal reactive functional groups can be controlled accurately, permitting detailed structure/performance information to be obtained. Functionalization of these polymeric nanoparticles with a DOTA-ligand capable of chelating radioactive Cu-64 nuclei enabled the biodistribution and in vivo positron emission tomography (PET) imaging of these materials to be studied and correlated directly to the initial structure. Results indicate that nanoparticles with increasing PEG shell thickness show increased blood circulation and low accumulation in excretory organs, suggesting application as in vivo carriers for imaging, targeting, and therapeutic groups.
引用
收藏
页码:1329 / 1339
页数:11
相关论文
共 65 条
[1]   Amphiphilic block copolymers for drug delivery [J].
Adams, ML ;
Lavasanifar, A ;
Kwon, GS .
JOURNAL OF PHARMACEUTICAL SCIENCES, 2003, 92 (07) :1343-1355
[2]   Design of environment-sensitive supramolecular assemblies for intracellular drug delivery: Polymeric micelles that are responsive to intracellular pH change [J].
Bae, Y ;
Fukushima, S ;
Harada, A ;
Kataoka, K .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2003, 42 (38) :4640-4643
[3]   Development of a universal alkoxyamine for "living" free radical polymerizations [J].
Benoit, D ;
Chaplinski, V ;
Braslau, R ;
Hawker, CJ .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1999, 121 (16) :3904-3920
[4]   A modular approach toward functionalized three-dimensional macromolecules:: From synthetic concepts to practical applications [J].
Bosman, AW ;
Vestberg, R ;
Heumann, A ;
Fréchet, JMJ ;
Hawker, CJ .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2003, 125 (03) :715-728
[5]   High-throughput synthesis of nanoscale materials:: Structural optimization of functionalized one-step star polymers [J].
Bosman, AW ;
Heumann, A ;
Klaerner, G ;
Benoit, D ;
Fréchet, JMJ ;
Hawker, CJ .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2001, 123 (26) :6461-6462
[6]   Poly(ethylene glycol)-coated hexadecylcyanoacrylate nanospheres display a combined effect for brain tumor targeting [J].
Brigger, I ;
Morizet, J ;
Aubert, G ;
Chacun, H ;
Terrier-Lacombe, MJ ;
Couvreur, P ;
Vassal, G .
JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS, 2002, 303 (03) :928-936
[7]   Polystyrene-block-poly(ethylene oxide) micelles in aqueous solution [J].
Bronstein, LM ;
Chernyshov, DM ;
Timofeeva, GI ;
Dubrovina, LV ;
Valetsky, PM ;
Khokhlov, AR .
LANGMUIR, 1999, 15 (19) :6195-6200
[8]   Photocrosslinked poly(vinylbenzophenone)-core micelles via mild Friedel-Crafts benzoylation of polystyrene amphiphiles [J].
Chen, Y ;
Tavakley, AE ;
Mathiason, TM ;
Taton, TA .
JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY, 2006, 44 (08) :2604-2614
[9]   From well defined star-microgels to highly ordered honeycomb films [J].
Connal, LA ;
Gurr, PA ;
Qiao, GG ;
Solomon, DH .
JOURNAL OF MATERIALS CHEMISTRY, 2005, 15 (12) :1286-1292
[10]  
Drummond DC, 1999, PHARMACOL REV, V51, P691