An Engineered Nanosugar Enables Rapid and Sustained Glucose‐Responsive Insulin Delivery in Diabetic Mice

Author:

Xu Rong1,Bhangu Sukhvir Kaur23,Sourris Karly C.4,Vanni Domitilla35,Sani Marc‐Antoine6,Karas John A.6,Alt Karen1,Niego Be'eri1,Ale Anukreity1,Besford Quinn A.3,Dyett Brendan2,Patrick Joshua1,Carmichael Irena7,Shaw Jonathan E.8,Caruso Frank3,Cooper Mark E.4,Hagemeyer Christoph E.1ORCID,Cavalieri Francesca25ORCID

Affiliation:

1. Australian Centre for Blood Diseases Central Clinical School Monash University Melbourne Victoria 3004 Australia

2. School of Science RMIT University Melbourne Victoria 3000 Australia

3. Department of Chemical Engineering The University of Melbourne Parkville Victoria 3000 Australia

4. Department of Diabetes Central Clinical School Monash University Melbourne Victoria 3004 Australia

5. Dipartimento di Scienze e Tecnologie Chimiche Universita’ di Roma “Tor Vergata” Via della Ricerca Scientifica 1 Rome 00133 Italy

6. School of Chemistry The Bio21 Institute The University of Melbourne Melbourne Victoria 3010 Australia

7. Monash Micro Imaging Monash University Melbourne Victoria 3004 Australia

8. Baker Heart and Diabetes Institute Melbourne Victoria 3004 Australia

Abstract

AbstractGlucose‐responsive insulin‐delivery platforms that are sensitive to dynamic glucose concentration fluctuations and provide both rapid and prolonged insulin release have great potential to control hyperglycemia and avoid hypoglycemia diabetes. Here, biodegradable and charge‐switchable phytoglycogen nanoparticles capable of glucose‐stimulated insulin release are engineered. The nanoparticles are “nanosugars” bearing glucose‐sensitive phenylboronic acid groups and amine moieties that allow effective complexation with insulin (≈95% loading capacity) to form nanocomplexes. A single subcutaneous injection of nanocomplexes shows a rapid and efficient response to a glucose challenge in two distinct diabetic mouse models, resulting in optimal blood glucose levels (below 200 mg dL–1) for up to 13 h. The morphology of the nanocomplexes is found to be key to controlling rapid and extended glucose‐regulated insulin delivery in vivo. These studies reveal that the injected nanocomplexes enabled efficient insulin release in the mouse, with optimal bioavailability, pharmacokinetics, and safety profiles. These results highlight a promising strategy for the development of a glucose‐responsive insulin delivery system based on a natural and biodegradable nanosugar.

Funder

National Health and Medical Research Council

Publisher

Wiley

Subject

Mechanical Engineering,Mechanics of Materials,General Materials Science

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