Selective synthesis of double temperature-sensitive polymer–peptide conjugates
- 16 July 2008
- journal article
- research article
- Published by Royal Society of Chemistry (RSC) in Chemical Communications
- No. 37,p. 4433-4435
- https://doi.org/10.1039/b806782a
Abstract
A novel synthetic route has been developed to couple selectively a modified octa-peptide, that is able to gel at low temperature, to the prototypical thermoresponsive polymer poly(N-isopropylacrylamide) to give a bioconjugate that exhibits double thermoresponsiveness.Keywords
This publication has 31 references indexed in Scilit:
- A review of stimuli-responsive nanocarriers for drug and gene deliveryJournal of Controlled Release, 2008
- Supramolecular Biomaterials. A Modular Approach towards Tissue EngineeringBulletin of the Chemical Society of Japan, 2007
- Synthesis of Stimuli-Responsive Polymers by Living Polymerization: Poly(N-Isopropylacrylamide) and Poly(Vinyl Ether)sPublished by Springer Nature ,2007
- Role of secondary structure changes on the morphology of polypeptide-based block copolymer vesiclesJournal of Colloid and Interface Science, 2007
- Protein binding to peptide-imprinted porous silica scaffoldsChemical Engineering Journal, 2007
- Polymer–drug conjugation, recent achievements and general strategiesProgress in Polymer Science, 2007
- Rod-Sphere Transition in Polybutadiene−Poly(l-lysine) Block Copolymer AssembliesLangmuir, 2007
- Dendrimers and dendritic polymers in drug deliveryDrug Discovery Today, 2005
- Functionalized Micellar Assemblies Prepared via Block Copolymers Synthesized by Living Free Radical Polymerization upon Peptide-Loaded ResinsBiomacromolecules, 2004
- Materials for enhancing cell adhesion by immobilization of cell‐adhesive peptideJournal of Biomedical Materials Research, 1991