| Literature DB >> 33177238 |
Zejun Wang1,2, Jinqiang Wang1,2,3, Hongjun Li1,2,3, Jicheng Yu4, Guojun Chen1,2, Anna R Kahkoska5, Valerie Wu1,2, Yi Zeng1,2, Di Wen1,2, Jayson R Miedema6,7, John B Buse5, Zhen Gu8,2,3,9.
Abstract
Reduced β-cell function and insulin deficiency are hallmarks of diabetes mellitus, which is often accompanied by the malfunction of glucagon-secreting α-cells. While insulin therapy has been developed to treat insulin deficiency, the on-demand supplementation of glucagon for acute hypoglycemia treatment remains inadequate. Here, we describe a transdermal patch that mimics the inherent counterregulatory effects of β-cells and α-cells for blood glucose management by dynamically releasing insulin or glucagon. The two modules share a copolymerized matrix but comprise different ratios of the key monomers to be "dually responsive" to both hyper- and hypoglycemic conditions. In a type 1 diabetic mouse model, the hybrid patch effectively controls hyperglycemia while minimizing the occurrence of hypoglycemia in the setting of insulin therapy with simulated delayed meal or insulin overdose.Entities:
Keywords: glucagon delivery; glucose-responsive; hypoglycemia; insulin delivery; microneedle patch
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Year: 2020 PMID: 33177238 PMCID: PMC7703584 DOI: 10.1073/pnas.2011099117
Source DB: PubMed Journal: Proc Natl Acad Sci U S A ISSN: 0027-8424 Impact factor: 11.205