Microgel encapsulated nanoparticles for glucose-responsive insulin delivery
Author(s)
Volpatti, Lisa R; Facklam, Amanda L.; Cortinas, Abel Bryan; Lu, Yen-Chun; Matranga, Morgan A.; MacIsaac, Corina; Hill, Michael C.; Langer, Robert S; Anderson, Daniel Griffith; ... Show more Show less
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An insulin delivery system that self-regulates blood glucose levels has the potential to limit hypoglycemic events and improve glycemic control. Glucose-responsive insulin delivery systems have been developed by coupling glucose oxidase with a stimuli-responsive biomaterial. However, the challenge of achieving desirable release kinetics (i.e., insulin release within minutes after glucose elevation and duration of release on the order of weeks) still remains. Here, we develop a glucose-responsive delivery system using encapsulated glucose-responsive, acetalated-dextran nanoparticles in porous alginate microgels. The nanoparticles respond rapidly to changes in glucose concentrations while the microgels provide them with protection and stability, allowing for extended glucose-responsive insulin release. This system reduces blood sugar in a diabetic mouse model at a rate similar to naked insulin and responds to a glucose challenge 3 days after administration similarly to a healthy animal. With 2 doses of microgels containing 60 IU/kg insulin each, we are able to achieve extended glycemic control in diabetic mice for 22 days.
Date issued
2020-11Department
Massachusetts Institute of Technology. Department of Chemical Engineering; Koch Institute for Integrative Cancer Research at MIT; Massachusetts Institute of Technology. Department of Biological EngineeringJournal
Biomaterials
Publisher
Elsevier BV
Citation
Volpatti, Lisa R. et al. "Microgel encapsulated nanoparticles for glucose-responsive insulin delivery." Biomaterials 267 (January 2021): 120458. © 2020
Version: Author's final manuscript
ISSN
0142-9612