You are not logged in Total: 7journals, 20,538articles Online
AccountAccount
Login / Register
Forgot Login?
 
Main menuMain menu
What's new
Journal list
Visiting ranking
Phrase ranking
Polls
About us
 
SearchSearch
 
Journal Site
Advanced Search
 

Home  >  Journal list  >  Polymer Journal  >  Vol.49  No.9 (2017)  >  pp.677-684

Polymer Journal
<<Previous article Vol.49  No.9 (2017)   pp.677 - 684 Next article>>

Analysis of the sol-to-gel transition behavior of temperature-responsive injectable polymer systems by fluorescence resonance energy transfer

Kazuyuki Takata1, Keisuke Kawahara1, Yasuyuki Yoshida1,2, Akinori Kuzuya1,3,4 and Yuichi Ohya1,3
1Department of Chemistry and Materials Engineering, Faculty of Chemistry, Materials and Bioengineering, Osaka, Japan
2Research Fellow of Japan Society for the promotion of Science, Tokyo, Japan
3Organization for Research and Development of Innovative Science and Technology (ORDIST), Kansai University, Osaka, Japan
4PREST, Japan Science and Technology Agency, Saitama, Japan

Amphiphilic triblock copolymers of poly(ethylene glycol) (PEG) and aliphatic polyesters such as poly(ε-caprolactone-co-glycolide) (PCGA) are typical examples of thermogelling polymers. In the gelation mechanism of these polymers, polymer chain transfer between the micelles, and subsequent aggregation of the micelles are important steps. We previously reported IP systems exhibiting temperature-responsive irreversible sol-gel transition that formed covalently cross-linked hydrogels. The IP formulation prepared by the ‘freeze–dry with PEG/dispersion’ method (D-sample) retained its sol state at r.t. longer than a formulation prepared by the usual dissolution method (S-sample). We hypothesized that polymer chain transfer between micelles was suppressed in the D-samples, because the micelle cores were in a solid-like state. In this study, we investigated polymer chain transfer by the fluorescence resonance energy transfer (FRET) method to reveal its role in the sol-to-gel transition. We synthesized a triblock copolymer of PCGA and PEG (tri-PCG) with attached naphthalene or dansyl groups at termini, tri-PCG-nap and tri-PCG-dan, as FRET donors and acceptors, respectively. The FRET behavior of the mixture of tri-PCG-nap/tri-PCG micelles and tri-PCG-dan/tri-PCG micelles was investigated. It was revealed that polymer chain transfer between micelles was strongly accelerated at the gelation temperature, and polymer chain transfer in D-samples was suppressed compared to S-samples.


Received: April 24, 2017 , Revised: May 31, 2017
Accepted: June 03, 2017 , Published online: July 12, 2017
© 2017 The Society of Polymer Science, Japan

NatureAbstract (Nature)


SPARC Japan

Terms of Use | Privacy Policy