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

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

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.

Keywords: diabetes; drug delivery; glucose-responsive; hypoxia-sensitive; microneedle.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Blood Glucose / analysis*
  • Diabetes Mellitus, Experimental / blood
  • Diabetes Mellitus, Experimental / drug therapy*
  • Diabetes Mellitus, Type 1 / blood
  • Diabetes Mellitus, Type 1 / drug therapy*
  • Drug Delivery Systems / instrumentation
  • Drug Delivery Systems / methods*
  • Glucose / metabolism
  • Glucose Oxidase / metabolism
  • Humans
  • Hyaluronic Acid / chemistry
  • Hyaluronic Acid / metabolism
  • Hypoglycemic Agents / administration & dosage
  • Hypoglycemic Agents / chemistry
  • Hypoxia / metabolism
  • Insulin / administration & dosage*
  • Insulin / chemistry
  • Insulin / metabolism
  • Male
  • Mice, Inbred C57BL
  • Microscopy, Electron, Transmission
  • Molecular Structure
  • Oxidation-Reduction
  • Reproducibility of Results

Substances

  • Blood Glucose
  • Hypoglycemic Agents
  • Insulin
  • Hyaluronic Acid
  • Glucose Oxidase
  • Glucose