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dc.contributor.authorNordli, Henriette R.
dc.contributor.authorPukstad, Brita
dc.contributor.authorChinga-Carrasco, Gary
dc.contributor.authorRokstad, Anne Mari
dc.date.accessioned2019-11-06T07:58:05Z
dc.date.available2019-11-06T07:58:05Z
dc.date.created2019-02-12T10:47:22Z
dc.date.issued2019
dc.identifier.citationACS Applied Bio Materials. 2019, .nb_NO
dc.identifier.issn2576-6422
dc.identifier.urihttp://hdl.handle.net/11250/2626780
dc.description.abstractUsing a lepirudin-based human whole blood model, we evaluated the initial inflammatory and coagulation responses of dense and porous ultrapure (<50 endotoxin units/grams) cellulose nanofibrils (CNF), of carboxylated grade. The CNF was compared to the wound dressing AquaCel because it is a potential wound-healing material. The porous CNF aerogels induced the strongest coagulation potential measured as prothrombin factor 1.2 (PTF1.2). AquaCel induced the strongest complement response by terminal complement complex (TCC) and surface C3c. All materials activated leukocytes CD11b, while the levels of only 3 of 27 cytokines were significantly changed, limited to (i) an elevation of the monocyte chemoattractant protein-1 (MCP-1/CCL) by the CNF aerogel, (ii) a reduction of eosinophil chemotactic proteins (eotaxin/CCL11) by the CNF aerogel, and (iii) a reduction of platelet-derived growth factor BB (PDGF-BB) by all CNF materials. In conclusion, the CNF materials and AquaCel differently activate coagulation, complement, and cytokines, improving the selection possibilities in various treatment situations of wound healing.nb_NO
dc.language.isoengnb_NO
dc.publisherAmerican Chemical Societynb_NO
dc.titleUltrapure Wood Nanocellulose - Assessments of Coagulation and Initial Inflammation Potentialnb_NO
dc.typeJournal articlenb_NO
dc.typePeer reviewednb_NO
dc.description.versionacceptedVersionnb_NO
dc.source.pagenumber12nb_NO
dc.source.journalACS Applied Bio Materialsnb_NO
dc.identifier.doi10.1021/acsabm.8b00711
dc.identifier.cristin1676290
dc.relation.projectSamarbeidsorganet mellom Helse Midt-Norge og NTNU: 46056819nb_NO
dc.relation.projectNorges forskningsråd: 219733nb_NO
dc.relation.projectNorges forskningsråd: 223255nb_NO
dc.description.localcodeLocked until 31.1.2020 due to copyright restrictions. This document is the Accepted Manuscript version of a Published Work that appeared in final form in [ACS Applied Bio Materials], copyright © American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see https://doi.org/10.1021/acsabm.8b00711nb_NO
cristin.unitcode194,65,15,0
cristin.unitcode1920,0,0,0
cristin.unitnameInstitutt for klinisk og molekylær medisin
cristin.unitnameSt. Olavs Hospital HF
cristin.ispublishedfalse
cristin.fulltextoriginal


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