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A novel delivery platform for therapeutic peptides.

DC Field Value Language
dc.contributor.authorPark, S-
dc.contributor.authorKim, SD-
dc.contributor.authorLee, HY-
dc.contributor.authorHwang, D-
dc.contributor.authorPark, JS-
dc.contributor.authorBae, YS-
dc.contributor.authorChung, J-
dc.date.accessioned2016-04-21T02:18:33Z-
dc.date.available2016-04-21T02:18:33Z-
dc.date.issued2014-
dc.identifier.issn0006-291X-
dc.identifier.urihttp://repository.ajou.ac.kr/handle/201003/12403-
dc.description.abstractAlthough many peptides have therapeutic effects against diverse disease, their

short half-lives in vivo hurdle their application as drug candidates. To extend

the short elimination half-lives of therapeutic peptides, we developed a novel

delivery platform for therapeutic peptides using an anti-hapten antibody and its

corresponding hapten. We selected cotinine because it is non-toxic, has a

well-studied metabolism, and is physiologically absent. We conjugated WKYMVm-NH2,

an anti-sepsis therapeutic peptide, to cotinine and showed that the conjugated

peptide in complex with an anti-cotinine antibody has a significantly improved in

vivo half-life while retaining its therapeutic efficacy. We suggest that this

novel delivery platform for therapeutic peptides will be very useful to develop

effective peptide therapeutics.
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dc.language.isoen-
dc.subject.MESHAnimals-
dc.subject.MESHCell Line-
dc.subject.MESHCotinine-
dc.subject.MESHDrug Compounding-
dc.subject.MESHDrug Delivery Systems-
dc.subject.MESHHumans-
dc.subject.MESHMice-
dc.subject.MESHNeutrophil Activation-
dc.subject.MESHNeutrophils-
dc.subject.MESHOligopeptides-
dc.subject.MESHProtein Binding-
dc.subject.MESHSepsis-
dc.subject.MESHTreatment Outcome-
dc.titleA novel delivery platform for therapeutic peptides.-
dc.typeArticle-
dc.identifier.pmid24857984-
dc.identifier.urlhttp://www.sciencedirect.com/science/article/pii/S0006291X14009127-
dc.contributor.affiliatedAuthor박, 준성-
dc.type.localJournal Papers-
dc.identifier.doi10.1016/j.bbrc.2014.05.049-
dc.citation.titleBiochemical and biophysical research communications-
dc.citation.volume450-
dc.citation.number1-
dc.citation.date2014-
dc.citation.startPage13-
dc.citation.endPage18-
dc.identifier.bibliographicCitationBiochemical and biophysical research communications, 450(1). : 13-18, 2014-
dc.identifier.eissn1090-2104-
dc.relation.journalidJ00006291X-
Appears in Collections:
Journal Papers > School of Medicine / Graduate School of Medicine > Hematology-Oncology
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