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dc.contributor.authorSauter, Alexanderen_US
dc.contributor.authorRichter, Guntheren_US
dc.contributor.authorMicoulet, Alexandreen_US
dc.contributor.authorMartinez, Auroraen_US
dc.contributor.authorSpatz, Joachim P.en_US
dc.contributor.authorAppel, Silkeen_US
dc.date.accessioned2014-07-08T08:01:52Z
dc.date.available2014-07-08T08:01:52Z
dc.date.issued2013-06-20eng
dc.identifier.issn1559-4106
dc.identifier.urihttps://hdl.handle.net/1956/8057
dc.description.abstractThe inhibition of unspecific adhesion of human white blood cells is a prerequisite for applications requiring the control of defined surface interactions. In this study, a passivation agent based on polyethylene glycol (PEG) for glass surfaces was investigated for the use with human peripheral blood mononuclear cells (PBMC). The grafting of 2000 g/mol methoxy-terminated PEG-urea-triethoxysilane (mPEG2000) onto glass surfaces successfully inhibited unspecific spreading of both human PBMC and platelets in all experiments. The prevention of surface interactions was independent on the anticoagulant used during blood collection. The total efficiency to prevent even transient immobilization of PBMC to the PEG modified surfaces was 97 ± 2%. This makes the passivation with PEG a well suited surface modification for preventing unspecific surface interaction in order to study only defined surface interactions of human PBMC.en_US
dc.language.isoengeng
dc.publisherSpringereng
dc.rightsAttribution CC BYeng
dc.rights.urihttp://creativecommons.org/licenses/by/2.0eng
dc.subjectPolyethylene glycoleng
dc.subjectPeripheral blood mononuclear cellseng
dc.subjectSurface passivationeng
dc.subjectUnspecific interactionseng
dc.titleEffective polyethylene glycol passivation for the inhibition of surface interactions of peripheral blood mononuclear cells and plateletsen_US
dc.typePeer reviewed
dc.typeJournal article
dc.date.updated2013-08-23T08:43:19Z
dc.description.versionpublishedVersionen_US
dc.rights.holderCopyright 2013 Sauter et al.; licensee Springer
dc.rights.holderAlexander Sauter et al.; licensee BioMed Central Ltd.
dc.source.articlenumber14
dc.identifier.doihttps://doi.org/10.1186/1559-4106-8-14
dc.identifier.cristin1051306
dc.source.journalBiointerphases
dc.source.408


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