Hyaluronic acid for anticancer drug and nucleic acid delivery

被引:482
作者
Dosio, Franco [1 ]
Arpicco, Silvia [1 ]
Stella, Barbara [1 ]
Fattal, Elias [2 ,3 ]
机构
[1] Univ Turin, Dipartimento Sci & Tecnol Farmaco, VP P Giuria 9, I-10125 Turin, Italy
[2] Univ Paris 11, Fac Pharm, Inst Galien Paris Sud, LabErr LERMIT, 5 Rue JB Clement, F-92296 Chatenay Malabry, France
[3] CNRS, UMR 8612, 5 Rue JB Clement, F-92296 Chatenay Malabry, France
关键词
Hyaluronic acid; Drug delivery systems; Nanotechnology; CD44; Conjugates; Anticancer agents; SELF-ASSEMBLED NANOPARTICLES; NANOSTRUCTURED LIPID CARRIERS; TUMOR-TARGETED DELIVERY; REDOX-SENSITIVE MICELLES; MESOPOROUS SILICA NANOPARTICLES; OVERCOMING MULTIDRUG-RESISTANCE; MULTIWALLED CARBON NANOTUBES; MOLECULAR-WEIGHT HYALURONAN; IN-VIVO BIODISTRIBUTION; POLYMERIC MICELLES;
D O I
10.1016/j.addr.2015.11.011
中图分类号
R9 [药学];
学科分类号
100702 [药剂学];
摘要
Hyaluronic acid (HA) is widely used in anticancer drug delivery, since it is biocompatible, biodegradable, nontoxic, and non-immunogenic; moreover, HA receptors are overexpressed on many tumor cells. Exploiting this ligand-receptor interaction, the use of HA is now a rapidly-growing platform for targeting CD44-overexpressing cells, to improve anticancer therapies. The rationale underlying approaches, chemical strategies, and recent advances in the use of HA to design drug carriers for delivering anticancer agents, are reviewed. Comprehensive descriptions are given of HA-based drug conjugates, particulate carriers (micelles, liposomes, nanopartides, microparticles), inorganic nanostructures, and hydrogels, with particular emphasis on reports of preclinical/clinical results. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:204 / 236
页数:33
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