| Literature DB >> 31978443 |
Cheng Zhang1, Sheng Hong1, Miao-Deng Liu1, Wu-Yang Yu1, Ming-Kang Zhang1, Lu Zhang1, Xuan Zeng2, Xian-Zheng Zhang3.
Abstract
Glucose-responsive insulin delivery system mimicking the function of pancreatic β-cells to maintain blood glucose homeostasis would effectively alleviate diabetes. Here, a new glucose-responsive delivery (ZIF@Ins&GOx) for self-regulated insulin release was constructed by encapsulating insulin and glucose oxidase (GOx) into pH-sensitive zeolitic imidazole framework-8 (ZIF-8) nanocrystals. After entering the cavities of ZIF-8, glucose can be oxidized into gluconic acid by GOx, causing a decrease in local pH. Then, ZIF-8 nanocrystals would be degraded under the acidic microenvironment that in turn triggers the release of insulin in a glucose responsive fashion. In vitro studies indicated that the biological activity of insulin could be protected by the rigid structure of ZIF-8 and the release of insulin could be modulated in response to glucose concentrations. In vivo experiments demonstrated that a single subcutaneous injection of the ZIF@Ins&GOx would facilitate the stabilization of blood glucose level of normoglycemic state for up to 72 h in type 1 diabetes (T1D). The multifunctional insulin delivery system shows a new proof-of-concept for T1D treatment by using ZIF-8 nanocrystals loaded with insulin and enzyme.Entities:
Keywords: Diabetes; Glucose oxidase; Glucose-response; Insulin; Metal-organic framework
Mesh:
Substances:
Year: 2020 PMID: 31978443 DOI: 10.1016/j.jconrel.2020.01.038
Source DB: PubMed Journal: J Control Release ISSN: 0168-3659 Impact factor: 9.776