Literature DB >> 17600338

Thermoresponsive degradable poly(ethylene glycol) analogues.

Na Wang1, Anjie Dong, Maciej Radosz, Youqing Shen.   

Abstract

Thermoresponsive polymers have many biomedical applications, but their nondegradability limits their in vivo applications. Herein, we report a new type of degradable thermoresponsive polymers-degradable poly (ethylene glycol) analogues (DPEGs) having lower critical solution temperatures (LCSTs) ranging 10-50 degrees C. DPEGs were synthesized by condensation polymerization of PEG-di(meth)acrylates (PEGDA or PEGDMA) with dithiols. Their LCSTs could be easily tuned by the PEG-chain length and the types of the double bond in the PEG monomers and dithiols. Long PEG chain and the presence of hydrophilic groups in the dithiol monomer increased the LCST of the resulting DPEG. Crosslinking DPEG chains produced thermoresponsive hydrogels. The hydrogels prepared by the end-capping method maintained the thermoresponsive properties of the linear DPEG. The degradable thermoresponsive DPEGs and their hydrogels have great potentials for in vivo biomedical applications. (c) 2007 Wiley Periodicals, Inc. J Biomed Mater Res, 2008.

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Year:  2008        PMID: 17600338     DOI: 10.1002/jbm.a.31466

Source DB:  PubMed          Journal:  J Biomed Mater Res A        ISSN: 1549-3296            Impact factor:   4.396


  2 in total

Review 1.  Protein-polymer conjugation-moving beyond PEGylation.

Authors:  Yizhi Qi; Ashutosh Chilkoti
Journal:  Curr Opin Chem Biol       Date:  2015-09-07       Impact factor: 8.822

2.  Poly[(ethylene oxide)-co-(methylene ethylene oxide)]: A hydrolytically-degradable poly(ethylene oxide) platform.

Authors:  Pontus Lundberg; Bongjae F Lee; Sebastiaan A van den Berg; Eric D Pressly; Annabelle Lee; Craig J Hawker; Nathaniel A Lynd
Journal:  ACS Macro Lett       Date:  2012-10-10       Impact factor: 6.903

  2 in total

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