4.7 Article

Galactose functionalized injectable thermoresponsive microgels for sustained protein release

Journal

COLLOIDS AND SURFACES B-BIOINTERFACES
Volume 113, Issue -, Pages 368-374

Publisher

ELSEVIER
DOI: 10.1016/j.colsurfb.2013.08.045

Keywords

Poly(NIPAAm-co-VAGA); Injectable microgels; Emulsion polymerization; Glycopolymer; Protein release

Funding

  1. National Natural Science Foundation of China [21303014]
  2. UK-China Joint Laboratory for Therapeutic Textiles
  3. State Key Laboratory for the Modification of Chemical Fibers and Polymer Materials
  4. Key Laboratory of Science 82 Technology of Eco-Textile, Donghua University, Ministry of Education
  5. Fundamental Research Funds for the Central Universities (Donghua University)

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Novel galactose functionalized thermoresponsive injectable microgels, poly(N-isopropylacrylamide-co-6-O-vinyladipoyl-D-galactose) P(NIPAAm-co-VAGA), have been fabricated using a combination of enzymatic transesterification and emulsion copolymerization. The microgels exhibit reversible temperature-responsive behavior, which can be tuned by varying the monomer feed ratio. The lower critical solution temperatures (LCSTs) of the materials are close to body temperature and can result in a rapid thermal gelation at 37 degrees C. Field emission scanning electron microscopy showed the resultant microgels to have porous structures, and dynamic light scattering experiments indicated a dramatic reduction in particle size as solutions of the polymers are heated through the LCST. The polymers can be loaded with protein (bovine serum albumin; BSA), and in vitro studies showed that the BSA release kinetics depend upon the temperature and copolymer composition. Microgels based on P(NIPAAm-co-VAGA) could hence serve as candidates for site-specific sustained release drug delivery systems. (C) 2013 Elsevier B.V. All rights reserved.

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