Cyclodextrin nanoassemblies: a promising tool for drug delivery

Autor: Cédric Gervaise, Catherine Sarazin, Florence Djedaïni-Pilard, Aurélien L. Furlan, Véronique Bonnet
Přispěvatelé: Génie Enzymatique et Cellulaire (GEC), Université de Technologie de Compiègne (UTC)-Université de Picardie Jules Verne (UPJV)-Centre National de la Recherche Scientifique (CNRS), Laboratoire de Glycochimie, des Antimicrobiens et des Agro-ressources - UMR CNRS 7378 (LG2A ), Institut de Chimie du CNRS (INC)-Université de Picardie Jules Verne (UPJV)-Centre National de la Recherche Scientifique (CNRS)
Rok vydání: 2015
Předmět:
Zdroj: Drug Discovery Today
Drug Discovery Today, Elsevier, 2015, 20, pp.1120-1126
Drug Discovery Today, Elsevier, 2015, 20 (9), pp.1120-1126. ⟨10.1016/j.drudis.2015.05.008⟩
ISSN: 1878-5832
1359-6446
Popis: International audience; Among the biodegradable and nontoxic compounds that can form nanoparticles for drug delivery, amphiphilic cyclodextrins are very promising. Apart from ionic cyclodextrins, which have been extensively studied and reviewed because of their application in gene delivery, our purpose is to provide a clear description of the supramolecular assemblies of nonionic amphiphilic cyclodextrins, which can form nanoassemblies for controlled drug release. Moreover, we focus on the relationship between their structure and physicochemical characteristics, which is crucial for self assembly and drug delivery. We also highlight the importance of the nanoparticle technology preparation for the stability and application of this nanodevice.
Databáze: OpenAIRE