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Updated: Jun 25, 2026

Measuring Relative Insulin Secretion using a Co-Secreted Luciferase Surrogate
Published on: June 25, 2019
Triggered release of insulin from glucose-sensitive enzyme multilayer shells
Wei Qi1, Xuehai Yan, Jinbo Fei
1Beijing National Laboratory for Molecular Sciences, International Joint Laboratory, Key Laboratory of Colloid and Interface Sciences, Institute of Chemistry, Chinese Academy of Sciences, China.
This study presents a novel glucose-sensitive multilayer shell for insulin delivery. The shell, made using layer-by-layer assembly, releases insulin in response to glucose levels, showing potential for advanced drug delivery systems.
Area of Science:
- Biomaterials Science
- Nanotechnology
- Drug Delivery Systems
Background:
- Insulin delivery systems require precise glucose responsiveness.
- Layer-by-layer (LbL) assembly offers a versatile platform for creating functional nanostructures.
- Controlled release of therapeutic proteins like insulin is a significant challenge.
Purpose of the Study:
- To develop a glucose-sensitive multilayer shell for insulin encapsulation and controlled release.
- To investigate the mechanism of glucose-induced insulin release from the fabricated core-shell system.
- To evaluate the potential of this system for advanced drug delivery applications.
Main Methods:
- Fabrication of a glucose-sensitive multilayer shell using layer-by-layer (LbL) assembly.
- Encapsulation of insulin within the multilayer structure.
- Assembly of glucose oxidase (GOD) and catalase (CAT) with glutaraldehyde (GA) cross-linking.
- Assessment of glucose-induced insulin release and microenvironment pH changes.
Main Results:
- The core-shell system demonstrated glucose sensitivity, with increased insulin release upon glucose introduction.
- Glucose catalysis by GOD/CAT shells led to H+ production, lowering the microenvironment pH.
- Acidic conditions promoted insulin release by breaking Schiff base bonds and increasing insulin solubility.
Conclusions:
- The developed CAT/GOD multilayer shell is a promising glucose-sensitive carrier for insulin delivery.
- The system's pH-dependent release mechanism offers a novel approach for controlled drug release.
- LbL capsules show significant potential for future applications in drug delivery and controlled release technologies.
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