| Literature DB >> 33685124 |
Jinqiang Wang1,2,3,4, Zejun Wang3,4, Guojun Chen3,4,5, Yanfang Wang1, Tianyuan Ci3,4, Hongjun Li1,3,4, Xiangsheng Liu4,6, Daojia Zhou3,4, Anna R Kahkoska7, Zhuxian Zhou8, Huan Meng3,6,9, John B Buse7, Zhen Gu1,2,3,4,9,10,11.
Abstract
Insulin therapy is the central component of treatment for type 1 and advanced type 2 diabetes; however, its narrow therapeutic window is associated with a risk of severe hypoglycemia. A glucose-responsive carrier that demonstrates consistent and slow basal insulin release under a normoglycemic condition and accelerated insulin release in response to hyperglycemia in real-time could offer effective blood glucose regulation with reduced risk of hypoglycemia. Here, we describe a poly(l-lysine)-derived biodegradable glucose-responsive cationic polymer for constructing polymer-insulin complexes for glucose-stimulated insulin delivery. The effects of the modification degree of arylboronic acid in the synthesized cationic polymer and polymer-to-insulin ratio on the glucose-dependent equilibrated free insulin level and the associated insulin release kinetics have been studied. In addition, the blood glucose regulation ability of these complexes and the associated glucose challenge-triggered insulin release are evaluated in type 1 diabetic mice.Entities:
Keywords: diabetes; drug delivery; glucose-responsive; insulin; stimuli-responsive release
Mesh:
Substances:
Year: 2021 PMID: 33685124 PMCID: PMC8210813 DOI: 10.1021/acsnano.0c07291
Source DB: PubMed Journal: ACS Nano ISSN: 1936-0851 Impact factor: 15.881