Organic nanoscale drug carriers coupled with ligands for targeted drug delivery in cancer

被引:65
作者
Shi, Meng [1 ,2 ,3 ]
Lu, Jiao [3 ,4 ]
Shoichet, Molly S. [1 ,2 ,3 ,4 ]
机构
[1] Univ Toronto, Dept Chem Engn & Appl Chem, Donnelly Ctr Cellular & Biomol Res 514, Toronto, ON M5S 3E1, Canada
[2] Univ Toronto, Inst Biomat & Biomed Engn, Donnelly Ctr Cellular & Biomol Res 514, Toronto, ON M5S 3E1, Canada
[3] Univ Toronto, Terrence Donnelly Ctr Cellular & Biomol Res, Donnelly Ctr Cellular & Biomol Res 514, Toronto, ON M5S 3E1, Canada
[4] Univ Toronto, Dept Chem, Donnelly Ctr Cellular & Biomol Res 514, Toronto, ON M5S 3E1, Canada
关键词
DIELS-ALDER REACTIONS; STERICALLY STABILIZED LIPOSOMES; POLY(LACTIC ACID) NANOPARTICLES; BLOCK-COPOLYMER MICELLES; IN-VITRO; CLICK CHEMISTRY; MULTIDRUG-RESISTANCE; MONOCLONAL-ANTIBODY; CIRCULATION TIME; CELLULAR UPTAKE;
D O I
10.1039/b822319j
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Nanoscale carriers are of increasing interest for use in anticancer therapy because they can deliver drugs in a targeted way. Ideally, nanocarriers combine passive and active delivery mechanisms, by integrating targeting ligands on the surface of their stealth corona using simple and efficient conjugation chemistry. This feature article summarizes the conventional and newly explored conjugation chemistries that are used to bind ligands in organic nanoparticle systems, providing strategic guidance for the preparation of targeted nanocarriers.
引用
收藏
页码:5485 / 5498
页数:14
相关论文
共 168 条
[1]   A strain-promoted [3+2] azide-alkyne cycloaddition for covalent modification of blomolecules in living systems [J].
Agard, NJ ;
Prescher, JA ;
Bertozzi, CR .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2004, 126 (46) :15046-15047
[2]   Development and brain delivery of chitosan-PEG nanoparticles functionalized with the monoclonal antibody OX26 [J].
Aktas, Y ;
Yemisci, M ;
Andrieux, K ;
Gürsoy, RN ;
Alonso, MJ ;
Fernandez-Megia, E ;
Novoa-Carballal, R ;
Quiñoá, E ;
Riguera, R ;
Sargon, MF ;
Çelik, HH ;
Demir, AS ;
Hincal, AA ;
Dalkara, T ;
Çapan, Y ;
Couvreur, P .
BIOCONJUGATE CHEMISTRY, 2005, 16 (06) :1503-1511
[3]   Controlling the physical behavior and biological performance of liposome formulations through use of surface grafted poly(ethylene glycol) [J].
Allen, C ;
Dos Santos, N ;
Gallagher, R ;
Chiu, GNC ;
Shu, Y ;
Li, WM ;
Johnstone, SA ;
Janoff, AS ;
Mayer, LD ;
Webb, MS ;
Bally, MB .
BIOSCIENCE REPORTS, 2002, 22 (02) :225-250
[4]   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
[5]   Ligand-targeted therapeutics in anticancer therapy [J].
Allen, TM .
NATURE REVIEWS CANCER, 2002, 2 (10) :750-763
[6]   A NEW STRATEGY FOR ATTACHMENT OF ANTIBODIES TO STERICALLY STABILIZED LIPOSOMES RESULTING IN EFFICIENT TARGETING TO CANCER-CELLS [J].
ALLEN, TM ;
BRANDEIS, E ;
HANSEN, CB ;
KAO, GY ;
ZALIPSKY, S .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES, 1995, 1237 (02) :99-108
[7]   Kinetic evaluation of the effect of layer by layer deposition of polyelectrolytes on the stability of POPC liposomes [J].
Angelini, G. ;
Boncompagni, S. ;
De Maria, P. ;
Fontana, A. ;
Gasbarri, C. ;
Siani, G. .
COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS, 2008, 322 (1-3) :234-238
[8]  
[Anonymous], 1987, Hetero Diels Alder methodology in Organic Synthesis
[9]   Cancer treatment by targeted drug delivery to tumor vasculature in a mouse model [J].
Arap, W ;
Pasqualini, R ;
Ruoslahti, E .
SCIENCE, 1998, 279 (5349) :377-380
[10]   Effect of copolymer composition on the physicochemical characteristics, in vitro stability, and biodistribution of PLGA-mPEG nanoparticles [J].
Avgoustakis, K ;
Beletsi, A ;
Panagi, Z ;
Klepetsanis, P ;
Livaniou, E ;
Evangelatos, G ;
Ithakissios, DS .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2003, 259 (1-2) :115-127