Microgel encapsulated nanoparticles for glucose-responsive insulin delivery

被引:40
|
作者
Volpatti, Lisa R. [1 ,2 ]
Facklam, Amanda L. [2 ,3 ]
Cortinas, Abel B. [1 ,2 ]
Lu, Yen-Chun [2 ,4 ]
Matranga, Morgan A. [1 ]
MacIsaac, Corina [2 ,5 ]
Hill, Michael C. [1 ]
Langer, Robert [1 ,2 ,3 ,4 ,5 ]
Anderson, Daniel G. [1 ,2 ,4 ,5 ]
机构
[1] MIT, Dept Chem Engn, Cambridge, MA 02139 USA
[2] MIT, David H Koch Inst Integrat Canc Res, 77 Massachusetts Ave, Cambridge, MA 02139 USA
[3] MIT, Dept Biol Engn, 77 Massachusetts Ave, Cambridge, MA 02139 USA
[4] Boston Childrens Hosp, Dept Anesthesiol, Boston, MA 02115 USA
[5] MIT, Harvard Mit Div Hlth Sci & Technol, Cambridge, MA 02139 USA
关键词
Glucose-responsive; Drug delivery; Microgels; Nanoparticles; Insulin; Diabetes; HYDROGELS; ALGINATE; IMMUNOISOLATION; COMPLICATIONS; CHALLENGES; ADHERENCE; VESICLES; REGIMENS; PROGRESS; DEXTRAN;
D O I
10.1016/j.biomaterials.2020.120458
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
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.
引用
收藏
页数:10
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