Hyaluronic acid (HA) is widely used in anticancer drug delivery, since it is biocompatible, biodegradable, non-toxic, 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, nanoparticles, microparticles), inorganic nanostructures, and hydrogels, with particular emphasis on reports of preclinical/clinical results.

Hyaluronic acid for anticancer drug and nucleic acid delivery

DOSIO, Franco;ARPICCO, Silvia Maria;STELLA, Barbara;
2016-01-01

Abstract

Hyaluronic acid (HA) is widely used in anticancer drug delivery, since it is biocompatible, biodegradable, non-toxic, 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, nanoparticles, microparticles), inorganic nanostructures, and hydrogels, with particular emphasis on reports of preclinical/clinical results.
2016
97
204
236
www.elsevier.com/locate/drugdeliv
Anticancer agents; CD44; Conjugates; Drug delivery systems; Hyaluronic acid; Nanotechnology; Animals; Antineoplastic Agents; Drug Carriers; Excipients; Humans; Hyaluronic Acid; Hydrogels; Nanostructures; Nucleic Acids; 3003
Dosio, Franco; Arpicco, Silvia; Stella, Barbara; Fattal, Elias
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2318/1532881
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