Related Experiment Video
Updated: Sep 7, 2025

High-throughput Synthesis of Carbohydrates and Functionalization of Polyanhydride Nanoparticles
Published on: July 6, 2012
Diboronate crosslinking: Introducing glucose specificity in glucose-responsive dynamic-covalent networks
Yuanhui Xiang1, Sijie Xian1, Rachel C Ollier1
1University of Notre Dame, Department of Chemical & Biomolecular Engineering, Notre Dame, IN 46556, USA.
New diboronate hydrogels offer improved glucose binding and specificity for diabetes management. This dynamic-covalent chemistry enables more responsive insulin release and better blood glucose control.
Area of Science:
- Materials Science
- Biomedical Engineering
- Polymer Chemistry
Background:
- Dynamic-covalent chemistry enables self-healing and stimuli-responsive hydrogels.
- Aryl boronate-diol interactions are explored for glucose-responsive insulin delivery.
- Existing phenylboronic acid (PBA) approaches suffer from low glucose affinity and specificity.
Purpose of the Study:
- To develop novel dynamic-covalent hydrogels with enhanced glucose binding affinity and specificity.
- To improve glucose-responsive insulin release for diabetes management.
- To overcome limitations of traditional PBA-based glucose-responsive materials.
Main Methods:
- Synthesis of novel diboronate crosslinking motifs.
- Preparation of dynamic-covalent hydrogels using the diboronate chemistry.
- In vitro and in vivo evaluation of glucose-responsive insulin release and blood glucose control in a rodent diabetes model.
Main Results:
- The new diboronate hydrogels exhibit enhanced binding affinity and specificity for glucose compared to PBA-based hydrogels.
- Diboronate hydrogels demonstrate improved glucose-responsive insulin release with minimal interference from non-glucose analytes.
- Enhanced responsiveness led to more rapid blood glucose correction in a rodent model.
Conclusions:
- Novel diboronate dynamic-covalent crosslinking chemistry offers superior glucose binding and specificity.
- These diboronate hydrogels represent a significant advancement for sensitive and specific glucose-responsive materials.
- This approach holds promise for improved diabetes management through advanced insulin delivery systems.
More Related Videos
13:35Structural Biology and Analytical Chemistry Approaches for Characterizing C-Glycoside Metabolic Enzymes in Human Gut Microbiota
Published on: May 23, 2025
08:46Regioselective O-Glycosylation of Nucleosides via the Temporary 2',3'-Diol Protection by a Boronic Ester for the Synthesis of Disaccharide Nucleosides
Published on: July 26, 2018
Related Concept Videos
Chemistry of Carbohydrates
Glucose Transporters
Facilitated diffusion-glucose transporters (GLUTs) are encoded by the solute-linked carrier (SLC) family 2, subfamily A gene family, or SLC2A. The 14 GLUT protein members are distributed into three classes:
Glucose Homeostasis: Regulation of Blood Glucose
During fasting, when blood glucose levels are low, the pancreas secretes glucagon. it...
Biosynthesis of Polysaccharides
Dehydration Synthesis
Dehydration synthesis (also called a condensation reaction) is the chemical process in which two molecules covalently link together to form a new molecule, along with the release of a water molecule. Many physiologically important compounds form by dehydration synthesis reactions, such as complex carbohydrates, proteins, DNA, and RNA.
Synthesis of carbohydrates
Sugar molecules are covalently linked together by dehydration synthesis. During the reaction, the hydroxyl (-OH) group from...
Network Covalent Solids
To break or to melt a covalent network solid, covalent bonds must be broken. Because covalent bonds are relatively strong, covalent network solids are typically...