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Microneedle-array patches loaded with hypoxia-sensitive vesicles provide fast glucose-responsive insulin delivery.

作者信息

Yu Jicheng, Zhang Yuqi, Ye Yanqi, DiSanto Rocco, Sun Wujin, Ranson Davis, Ligler Frances S, Buse John B, Gu Zhen

机构信息

Joint Department of Biomedical Engineering, University of North Carolina at Chapel Hill and North Carolina State University, Raleigh, NC 27695; Molecular Pharmaceutics Division and Center for Nanotechnology in Drug Delivery, Eshelman School of Pharmacy, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599;

Joint Department of Biomedical Engineering, University of North Carolina at Chapel Hill and North Carolina State University, Raleigh, NC 27695;

出版信息

Proc Natl Acad Sci U S A. 2015 Jul 7;112(27):8260-5. doi: 10.1073/pnas.1505405112. Epub 2015 Jun 22.


DOI:10.1073/pnas.1505405112
PMID:26100900
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4500284/
Abstract

A glucose-responsive "closed-loop" insulin delivery system mimicking the function of pancreatic cells has tremendous potential to improve quality of life and health in diabetics. Here, we report a novel glucose-responsive insulin delivery device using a painless microneedle-array patch ("smart insulin patch") containing glucose-responsive vesicles (GRVs; with an average diameter of 118 nm), which are loaded with insulin and glucose oxidase (GOx) enzyme. The GRVs are self-assembled from hypoxia-sensitive hyaluronic acid (HS-HA) conjugated with 2-nitroimidazole (NI), a hydrophobic component that can be converted to hydrophilic 2-aminoimidazoles through bioreduction under hypoxic conditions. The local hypoxic microenvironment caused by the enzymatic oxidation of glucose in the hyperglycemic state promotes the reduction of HS-HA, which rapidly triggers the dissociation of vesicles and subsequent release of insulin. The smart insulin patch effectively regulated the blood glucose in a mouse model of chemically induced type 1 diabetes. The described work is the first demonstration, to our knowledge, of a synthetic glucose-responsive device using a hypoxia trigger for regulation of insulin release. The faster responsiveness of this approach holds promise in avoiding hyperglycemia and hypoglycemia if translated for human therapy.

摘要

相似文献

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本文引用的文献

[1]
Glucose-responsive insulin activity by covalent modification with aliphatic phenylboronic acid conjugates.

Proc Natl Acad Sci U S A. 2015-2-24

[2]
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Nat Rev Drug Discov. 2014-11-28

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Nat Nanotechnol. 2014-11

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Biomacromolecules. 2014-10-13

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Nat Commun. 2014-6-17

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Nat Commun. 2014-3-11

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Nat Commun. 2013

[9]
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ACS Nano. 2013-7-8

[10]
Injectable nano-network for glucose-mediated insulin delivery.

ACS Nano. 2013-5-2

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