Noncovalent functionalization of mesoporous silica nanoparticles with amphiphilic peptides

buir.contributor.authorGüler, Mustafa O.
dc.citation.epage2174en_US
dc.citation.issueNumber15en_US
dc.citation.spage2168en_US
dc.citation.volumeNumber2en_US
dc.contributor.authorSardan, M.en_US
dc.contributor.authorYildirim, A.en_US
dc.contributor.authorMumcuoglu, D.en_US
dc.contributor.authorTekinay, A. B.en_US
dc.contributor.authorGüler, Mustafa O.en_US
dc.date.accessioned2016-02-08T10:56:16Z
dc.date.available2016-02-08T10:56:16Z
dc.date.issued2014en_US
dc.departmentNanotechnology Research Center (NANOTAM)en_US
dc.departmentInstitute of Materials Science and Nanotechnology (UNAM)en_US
dc.description.abstractThe surface of mesoporous silica nanoparticles (MSNs) has been modified for enhancing their cellular uptake, cell targeting, bioimaging, and controlled drug release. For this purpose, covalent anchorage on the silica surface was predominantly exploited with a wide range of bioactive molecules. Here, we describe a facile self-assembly method to prepare a hybrid peptide silica system composed of octyl-modified mesoporous silica nanoparticles (MSNs) and peptide amphiphiles (PAs). The hydrophobic organosilane surface of mesoporous silica was coated with amphiphilic peptide molecules. The peptide functionalized particles exhibited good cyto-compatibility with vascular smooth muscle and vascular endothelial cells. The peptide coating also improved the cellular uptake of particles up to 6.3 fold, which is promising for the development of highly efficient MSN based theranostic agents. © 2014 the Partner Organisations.en_US
dc.description.provenanceMade available in DSpace on 2016-02-08T10:56:16Z (GMT). No. of bitstreams: 1 bilkent-research-paper.pdf: 70227 bytes, checksum: 26e812c6f5156f83f0e77b261a471b5a (MD5) Previous issue date: 2014en
dc.identifier.doi10.1039/c4tb00037den_US
dc.identifier.issn20507518
dc.identifier.urihttp://hdl.handle.net/11693/26191
dc.language.isoEnglishen_US
dc.publisherRoyal Society of Chemistryen_US
dc.relation.isversionofhttps://doi.org/10.1039/c4tb00037den_US
dc.source.titleJournal of Materials Chemistry Ben_US
dc.subjectAmphiphilic peptidesen_US
dc.subjectControlled drug releaseen_US
dc.subjectFunctionalized particlesen_US
dc.subjectMesoporous silica nanoparticlesen_US
dc.subjectNon-covalent functionalizationen_US
dc.subjectSelf-assembly methoden_US
dc.subjectVascular endothelial cellsen_US
dc.subjectVascular smooth musclesen_US
dc.subjectEndothelial cellsen_US
dc.subjectPolymer blendsen_US
dc.subjectSilicaen_US
dc.subjectPeptidesen_US
dc.titleNoncovalent functionalization of mesoporous silica nanoparticles with amphiphilic peptidesen_US
dc.typeArticleen_US

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