Abstract |
Although 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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Authors | Sunyoung Park, Sang Doo Kim, Ha Young Lee, Dobeen Hwang, Joon Seong Park, Yoe-Sik Bae, Junho Chung |
Journal | Biochemical and biophysical research communications
(Biochem Biophys Res Commun)
Vol. 450
Issue 1
Pg. 13-8
(Jul 18 2014)
ISSN: 1090-2104 [Electronic] United States |
PMID | 24857984
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Copyright | Copyright © 2014 Elsevier Inc. All rights reserved. |
Chemical References |
- Oligopeptides
- Trp-Lys-Tyr-Met-Val-Met
- Cotinine
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Topics |
- Animals
- Cell Line
- Cotinine
(administration & dosage, chemistry, pharmacokinetics)
- Drug Compounding
(methods)
- Drug Delivery Systems
(methods)
- Humans
- Mice
- Neutrophil Activation
(drug effects)
- Neutrophils
(drug effects, metabolism)
- Oligopeptides
(administration & dosage, chemistry, pharmacokinetics)
- Protein Binding
- Sepsis
(diagnosis, drug therapy)
- Treatment Outcome
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