Abstract

Novel and well-defined amphiphilic dendrimer-star copolymer poly(e-caprolactone)-block-(poly(2-(2-methoxyethoxy)ethylmethacrylate-co-oligo(ethylene glycol) methacrylate))2 with Y-shaped arms were synthesized by the combination of ring-opening polymerization (ROP) and atom transfer radical polymerization (ATRP). The investigation of thermal properties and the analysis of crystalline morphology indicate that the high-branched structure of dendrimer-star copolymers with Y-shaped arms and the presence of amorphous P(MEO2MA-co-OEGMA) segments together led to the complete destruction of crystallinity of the PCL segments in the dendrimer-star copolymer. In addition, the hydrophilicity–hydrophobicity transition of the dendrimer-star copolymer film can be achieved by altering the external temperatures. The amphiphilic copolymers can self-assemble into spherical nanomicelles in water. Because the lower critical solution temperature of the copolymers can be adjusted by varying the ratio of MEO2MA and OEGMA, the tunable thermosensitive properties can be observed by transmittance, dynamic laser light scattering, and transmission electron microscopy (TEM). The release rate of model drug chlorambucil from the micelles can be effectively controlled by changing the external temperatures, which indicates that these unique high-branched amphiphilic copolymers have the potential applications in biomedical field. © 2011 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2011

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.