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Click chemistry for drug delivery nanosystems.

Authors :
Lallana E
Sousa-Herves A
Fernandez-Trillo F
Riguera R
Fernandez-Megia E
Source :
Pharmaceutical research [Pharm Res] 2012 Jan; Vol. 29 (1), pp. 1-34. Date of Electronic Publication: 2011 Sep 13.
Publication Year :
2012

Abstract

The purpose of this Expert Review is to discuss the impact of click chemistry in nanosized drug delivery systems. Since the introduction of the click concept by Sharpless and coworkers in 2001, numerous examples of click reactions have been reported for the preparation and functionalization of polymeric micelles and nanoparticles, liposomes and polymersomes, capsules, microspheres, metal and silica nanoparticles, carbon nanotubes and fullerenes, or bionanoparticles. Among these click processes, Cu(I)-catalyzed azide-alkyne cycloaddition (CuAAC) has attracted most attention based on its high orthogonality, reliability, and experimental simplicity for non-specialists. A renewed interest in the use of efficient classical transformations has been also observed (e.g., thiol-ene coupling, Michael addition, Diels-Alder). Special emphasis is also devoted to critically discuss the click concept, as well as practical aspects of application of CuAAC to ensure efficient and harmless bioconjugation.

Details

Language :
English
ISSN :
1573-904X
Volume :
29
Issue :
1
Database :
MEDLINE
Journal :
Pharmaceutical research
Publication Type :
Academic Journal
Accession number :
21913032
Full Text :
https://doi.org/10.1007/s11095-011-0568-5