PEG-grafted chitosan as an injectable thermosensitive hydrogel for sustained protein release.
By N. Bhattarai, Hassna R. Ramay, J. Gunn, Miqin Zhang. Journal of Controlled Release, 2005
619 citations recorded by the source corpus.
Subfields: Molecular Medicine, Pharmaceutical Science, Surfaces, Coatings and Films
View Paper: https://www.semanticscholar.org/paper/520fa293eacc840f09fb52e2f7b1382966e14dd4
How researchers see this paper
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In Molecular Medicine
- E. Chiellini
- C. Jérôme
- Nicholas A. Peppas
- R. Ottenbrite
- Florence Croisier
- Federica Chiellini
- M. Dash
- N. Bhattarai
In Pharmaceutical Science
In Surfaces, Coatings and Films
Citations in the corpus
- Chitosan-based hydrogels for controlled, localized drug delivery. (2010, methodology): “Use of genipin also showed extended drug release by chitosan hydrogels cross-linked in situ [75,92].”
- Chitosan—A versatile semi-synthetic polymer in biomedical applications (2011, background): “Genipin also provides extended drug release by chitosan hydrogels cross-linked in situ [179,190].”
- Chitosan-based biomaterials for tissue engineering (2013, background): “Chitosan structure can also be modified to form physical hydrogels: chitosan-g-poly(ethylene glycol) (PEG) graft copolymer is able of self-organization depending on the temperature to form stable hydrogels [73].”
- Natural origin biodegradable systems in tissue engineering and regenerative medicine: present status and some moving trends (2007, background): “2005 a , b ) and polyethylene glycol (PEG; Bhattarai et al .”
- Polymers for Drug Delivery Systems (2010, methodology): “This approach was used in a study describing the release of model protein bovine serum albumin (BSA) from temperature-responsive chitosan grafted with PEG (PEG-g-chitosan) (55).”