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dc.contributor.authorKalafatovic, D.*
dc.contributor.authorNobis, M.*
dc.contributor.authorJavid, Nadeem*
dc.contributor.authorFrederix, P.W.J.M.*
dc.contributor.authorAnderson, K.I.*
dc.contributor.authorSaunders, B.R.*
dc.contributor.authorUlijn, R.V.*
dc.date.accessioned2017-02-21T10:17:28Z
dc.date.available2017-02-21T10:17:28Z
dc.date.issued2014-10-28
dc.identifier.citationKalafatovic D, Nobis M, Javid N et al (2015) MMP-9 triggered micelle-to-fibre transitions for slow release of doxorubicin. Biomaterials Sciences. 3(2): 246-249.en_US
dc.identifier.urihttp://hdl.handle.net/10454/11430
dc.descriptionYesen_US
dc.description.abstractPhenylacetyl-peptide amphiphiles were designed, which upon cleavage by a disease-associated enzyme reconfigure from micellar aggregates to fibres. Upon this morphological change, a doxorubicin payload could be retained in the fibres formed, which makes them valuable carriers for localised formation of nanofibre depots for slow release of hydrophobic anticancer drugs.en_US
dc.language.isoenen_US
dc.relation.isreferencedbyhttp://dx.doi.org/10.1039/C4BM00297Ken_US
dc.rights(c) 2015 The Authors. This is an Open Access article distributed under the Creative Commons CC-BY license (http://creativecommons.org/licenses/by/3.0/)en_US
dc.subjectCancer; Doxorubicin; Self-assembly; Peptideen_US
dc.titleMMP-9 triggered micelle-to-fibre transitions for slow release of doxorubicinen_US
dc.status.refereedYesen_US
dc.date.Accepted2014-10-09
dc.date.application2014-10-28
dc.typeArticleen_US
dc.type.versionPublished versionen_US
refterms.dateFOA2018-07-26T09:49:37Z


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