[PDF] Oral insulin delivery using P(MAA-g-EG) hydrogels: effects of network morphology on insulin delivery characteristics.

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DOI:10.1016/J.JCONREL.2003.12.022
Corpus ID: 17899959

@article{Nakamura2004OralID, title={Oral insulin delivery using P(MAA-g-EG) hydrogels: effects of network morphology on insulin delivery characteristics.}, author={Koji Nakamura and Robert John Murray and Jeffrey I. Joseph and Nicholas A. Peppas and Mariko Morish*ta and Anthony M. Lowman}, journal={Journal of controlled release : official journal of the Controlled Release Society}, year={2004}, volume={95 3}, pages={ 589-99 }, url={https://api.semanticscholar.org/CorpusID:17899959}}

Koji Nakamura, R. Murray, A. Lowman
Published in Journal of Controlled Release 24 March 2004
Materials Science, Medicine

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Oral delivery of insulin using pH-responsive complexation gels.

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P pH-responsive, poly(methacrylic-g-ethylene glycol) hydrogels are investigated as oral delivery vehicles for insulin to protect the sensitive drug from proteolytic degradation in the stomach and upper portion of the small intestine.

Mucosal insulin delivery systems based on complexation polymer hydrogels: effect of particle size on insulin enteral absorption.

M. Morish*taTakahiro Goto A. Lowman

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Elucidation of the mechanism of incorporation of insulin in controlled release systems based on complexation polymers.

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Graft copolymer networks of poly(methacrylic acid-g-ethylene glycol) exhibiting pH-dependent swelling behavior due to the formation of interpolymer complexes were prepared by free radical solution…

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M. A. ArangoaG. PonchelA. OrecchioniM. RenedoD. DuchěneJ. Irache

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E. HosnyH. I. Al-ShoraM. Elmazar

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In vivo effects of highly purified docosahexaenoic acid on rectal insulin absorption.

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