Glucose-Responsive Microgels Integrated with Enzyme Nanocapsules for Closed-Loop Insulin Delivery

被引:338
作者
Gu, Zhen [1 ,2 ,3 ,5 ,6 ,7 ]
Dang, Tram T. [1 ,2 ,3 ]
Ma, Minglin [1 ,2 ,3 ]
Tang, Benjamin C. [1 ,2 ,3 ]
Cheng, Hao [1 ,2 ]
Jiang, Shan [1 ,2 ]
Dong, Yizhou [1 ,2 ,3 ]
Zhang, Yunlong [1 ,2 ,3 ]
Anderson, Daniel G. [1 ,2 ,3 ,4 ]
机构
[1] MIT, Dept Chem Engn, Cambridge, MA 02139 USA
[2] MIT, David H Koch Inst Integrat Canc Res, Cambridge, MA 02139 USA
[3] Childrens Hosp Boston, Dept Anesthesiol, Boston, MA 02115 USA
[4] MIT, Div Hlth Sci & Technol, Cambridge, MA 02139 USA
[5] Univ North Carolina Chapel Hill, Joint Dept Biomed Engn, Raleigh, NC 27695 USA
[6] N Carolina State Univ, Raleigh, NC 27695 USA
[7] Univ North Carolina Chapel Hill, Eshelman Sch Pharm, Mol Pharmaceut Div, Chapel Hill, NC 27599 USA
关键词
drug delivery; diabetes; insulin; glucose-responsive; nanocapsules; microgels; CATIONIC COPOLYMER HYDROGELS; RELEASE; SYSTEMS; OXIDASE; NANOGEL;
D O I
10.1021/nn401617u
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A glucose-responsive dosed-loop insulin delivery system represents the ideal treatment of type 1 diabetes mellitus. In this study, we develop uniform injectable microgels for controlled glucose-responsive release of insulin. Monodisperse microgels (256 +/- 18 mu m), consisting of a pH responsive chitosan matrix, enzyme nanocapsules, and, recombinant human insulin were fabricated through a one-step electrospray procedure. Glucose-specific enzymes were covalently encapsulated into the nanocapsules to Improve enzymatic stability by protecting from denaturation and immunogenicity as well as to minimize loss due to diffusion from the matrix. The microgel system swelled when subjected to hyperglycemic conditions, as a result of the enzymatic conversion of glucose into gluconic acid and protonation of the chitosan network. Acting as a self-regulating valve system, microgels were adjusted to release insulin at basal release rates under normoglycemic conditions and at higher rates under hyperglycemic conditions. Finally, we demonstrated that these microgels with enzyme nanocapsules facilitate insulin release and result in a reduction of blood glucose levels in a mouse model of type 1 diabetes.
引用
收藏
页码:6758 / 6766
页数:9
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