Redox-responsive micellar nanoparticles from glycosaminoglycans for CD44 targeted drug delivery

last updated: 2018-05-15
ProjectCytoNanoHeal :: publications list
TitleRedox-responsive micellar nanoparticles from glycosaminoglycans for CD44 targeted drug delivery
Publication TypePapers in Scientific Journals
Year of Publication2018
AuthorsCarvalho A. M., Teixeira R., Novoa-Carballal R., Pires R. A., Reis R. L., and Pashkuleva I.
Abstract

Cancer progression is associated with overexpression of various receptors at the cell surface. Among these, CD44 is known to recognize and bind specifically hyaluronan (HA) and interact with less affinity to other glycosaminoglycans (GAGs), such as chondroitin sulfate (CS). In this study, we describe a simple method to obtain micellar nanoparticles with GAGs shell (HA or CS) as potential drug delivery systems that target cancer cells overexpressing CD44. Alkane thiol was conjugated at the reducing end of the respective GAG using highly efficient oxime chemistry. The alkane moiety confers amphiphilic behavior to the obtained conjugates and trigger their self-assembly into micellar nanoparticles, while the thiol group add redox-responsiveness to the system. The properties of the particles depend on the used GAG: HA amphiphiles form more dense, smaller assemblies that are redox sensitive. Both systems allow encapsulation of either hydrophobic or hydrophilic cargos with high efficiency. We demonstrate that the GAGs exposed on the surface of the nanoparticles are with preserved bioactivity and recognized by the cellular receptors: the particles were internalized via CD44 dependent pathways. 

JournalBiomacromolecules
Volume19
Paginationin press
Date Published2018-05-14
PublisherACS
ISSN1526-4602
DOI10.1021/acs.biomac.8b00561
URLhttps://pubs.acs.org/doi/pdf/10.1021/acs.biomac.8b00561
KeywordsCD44, chondroitin sulfate, Hyaluronic acid, micellar nanoparticles, self-assembly
RightsembargoedAccess (2 Years)
Peer reviewedyes
Statuspublished

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