Fate of micelles and quantum dots in cells

被引:126
作者
Maysinger, Dusica
Lovric, Jasmina
Eisenberg, Adi
Savic, Radoslav
机构
[1] McGill Univ, Dept Pharmacol & Therapeut, Montreal, PQ H3G 1Y6, Canada
[2] Univ Zagreb, Dept Pharmaceut Technol, Zagreb 41000, Croatia
[3] McGill Univ, Dept Chem, Montreal, PQ, Canada
基金
加拿大健康研究院;
关键词
block copolymer micelles; quantum dots; internalization; stability; confocal microscopy; multiple labeling; fluorescent dyes; organelles;
D O I
10.1016/j.ejpb.2006.08.011
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Micelles and quantum dots have been used as experimental drug delivery systems and imaging tools both in vitro and in vivo. Investigations of their fate at the subcellular level require different surface-core modifications. Among the most common modifications are those with fluorescent probes, dense-core metals or radionucleids. Cellular fate of several fluorescent probes incorporated into poly(caprolactone)-b-copolymer micelles (PCL-b-PEO) was followed by confocal microscopy, and colloidal gold incorporated in poly 4-vinyl pyridine-PEO micelles were developed to explore micelle fate by electron microscopy. More recently, we have examined quantum dots (QDs) as the next-generation-labels for cells and nanoparticulate drug carriers amenable both to confocal and electron microscopic analyses. Effects of QDs at the cellular and subcellular levels and their integrity were studied. Results from different studies suggest that size, charge and surface manipulations of QDs may play a role in their subcellular distribution. Examples of pharmacological agents incorporated into block copolymer micelles, administered or attached to QD surfaces show how the final biological outcome (e.g. cell death, proliferation or differentiation) depends on physical properties of these nanoparticles. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:270 / 281
页数:12
相关论文
共 138 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]   Relative aggregation state and hemolytic activity of amphotericin B encapsulated by poly(ethylene oxide)-block-poly(N-hexyl-L-aspartamide)-acyl conjugate micelles:: effects of acyl chain length [J].
Adams, ML ;
Kwon, GS .
JOURNAL OF CONTROLLED RELEASE, 2003, 87 (1-3) :23-32
[3]   Amphotericin B encapsulated in micelles based on poly(ethylene oxide)-block-poly(L-amino acid) derivatives exerts reduced in vitro hemolysis but maintains potent in vivo antifungal activity [J].
Adams, ML ;
Andes, DR ;
Kwon, GS .
BIOMACROMOLECULES, 2003, 4 (03) :750-757
[4]   Nanocrystal targeting in vivo [J].
Åkerman, ME ;
Chan, WCW ;
Laakkonen, P ;
Bhatia, SN ;
Ruoslahti, E .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (20) :12617-12621
[5]   Size-dependent dissociation pH of thiolate ligands from cadmium chalcogenide nanocrystals [J].
Aldana, J ;
Lavelle, N ;
Wang, YJ ;
Peng, XG .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2005, 127 (08) :2496-2504
[6]   Photochemical instability of CdSe nanocrystals coated by hydrophilic thiols [J].
Aldana, J ;
Wang, YA ;
Peng, XG .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2001, 123 (36) :8844-8850
[7]   Polycaprolactone-b-poly(ethylene oxide) copolymer micelles as a delivery vehicle for dihydrotestosterone [J].
Allen, C ;
Han, JN ;
Yu, YS ;
Maysinger, D ;
Eisenberg, A .
JOURNAL OF CONTROLLED RELEASE, 2000, 63 (03) :275-286
[8]  
Allen C, 2000, DRUG DELIV, V7, P139
[9]   Nano-engineering block copolymer aggregates for drug delivery [J].
Allen, C ;
Maysinger, D ;
Eisenberg, A .
COLLOIDS AND SURFACES B-BIOINTERFACES, 1999, 16 (1-4) :3-27
[10]   Influence of the surfactant concentration on the body distribution of nanoparticles [J].
Araujo, L ;
Löbenberg, R ;
Kreuter, J .
JOURNAL OF DRUG TARGETING, 1999, 6 (05) :373-385