Diboronate-Modified Hyaluronic Acid for Glucose-Responsive Insulin Delivery

Diabetes requires precise insulin management to maintain glycemic control and prevent severe complications. Glucose-responsive delivery systems envision an autonomous approach to improve insulin therapy. Here, a glucose-sensitive insulin delivery system comprising hyaluronic acid conjugated with a diboronate glucose binder as a carrier for diol-modified insulin is shown. This approach seeks improved precision in insulin delivery, leveraging bidentate glucose binding to achieve enhanced glucose affinity and specificity. Modification of insulin with a diol motif preserves its native conformation and function. These insulin formulations correct blood glucose in diabetic mice, including glucose-responsive function when subjected to a glucose challenge. However, the absence of secondary interactions, such as electrostatic complexation, ultimately limits the duration of function relative to that of previous platforms. Integrating complementary interactions alongside dynamic-covalent glucose binders therefore enhances the functional duration and therapeutic efficacy in the design of glucose-responsive polymeric carriers, offering design insights into the development of new carriers for glucose-responsive insulin delivery.

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Publication Details

Journal
Biomacromolecules
Published
2025-03-27
DOI
https://doi.org/10.1021/acs.biomac.5c00144
Citations
3
Primary Topic
Pancreatic function and diabetes
Type
article
Field-Weighted Citation Impact
6.02

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article

Diboronate-Modified Hyaluronic Acid for Glucose-Responsive Insulin Delivery

Jiřı́ Jiráček, Yuanhui Xiang, Sijie Xian, Katarína Mitrová et al.
3 citations
Biomacromolecules
Pancreatic function and diabetes
6.02
article

Diboronate-Modified Hyaluronic Acid for Glucose-Responsive Insulin Delivery

Jiřı́ Jiráček, Yuanhui Xiang, Sijie Xian, Katarína Mitrová, Matthew J. Webber
article en
3 citations

Abstract

Diabetes requires precise insulin management to maintain glycemic control and prevent severe complications. Glucose-responsive delivery systems envision an autonomous approach to improve insulin therapy. Here, a glucose-sensitive insulin delivery system comprising hyaluronic acid conjugated with a diboronate glucose binder as a carrier for diol-modified insulin is shown. This approach seeks improved precision in insulin delivery, leveraging bidentate glucose binding to achieve enhanced glucose affinity and specificity. Modification of insulin with a diol motif preserves its native conformation and function. These insulin formulations correct blood glucose in diabetic mice, including glucose-responsive function when subjected to a glucose challenge. However, the absence of secondary interactions, such as electrostatic complexation, ultimately limits the duration of function relative to that of previous platforms. Integrating complementary interactions alongside dynamic-covalent glucose binders therefore enhances the functional duration and therapeutic efficacy in the design of glucose-responsive polymeric carriers, offering design insights into the development of new carriers for glucose-responsive insulin delivery.

BiomacromoleculesVol. 26(4)
University of Notre Dame (US), Czech Academy of Sciences (CZ), Czech Academy of Sciences, Institute of Organic Chemistry and Biochemistry (CZ)
National Science Foundation, American Diabetes Association, Leona M. and Harry B. Helmsley Charitable Trust
Good health and well-being
Openalex Percentile: Top 5%
Pancreatic function and diabetes
6.02
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Diboronate-Modified Hyaluronic Acid for Glucose-Responsive Insulin Delivery — Jiřı́ Jiráček, Yuanhui Xiang, et al. · Biomacromolecules (2025) | TGRS Research Map | TGRS