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Published on: June 25, 2017
Modeling the response time of an in vivo glucose affinity sensor
H R Clark1, T A Barbari, G Rao
1Medical Biotechnology Center and Department of Chemical and iochemical Engineering, University of Maryland, Baltimore, Maryland 21201, USA.
A mathematical model predicts optical glucose sensor performance, identifying membrane diffusion as key to response time. External factors like boundary layers and fibrotic capsules significantly slow sensor readings.
Area of Science:
- Biomedical Engineering
- Chemical Engineering
- Analytical Chemistry
Background:
- Optical glucose sensors rely on competitive displacement assays for glucose detection.
- Fluorescent lifetime measurements track ligand-receptor interactions.
- Hollow fiber membranes are used to encapsulate sensor components.
Purpose of the Study:
- To develop a mathematical model for an optical glucose sensor's dose-response relationship.
- To predict sensor response time under various conditions.
- To investigate the impact of environmental factors on sensor performance.
Main Methods:
- Developed a numerical model incorporating glucose diffusion and displacement reactions.
- Simulated the effect of external mass transfer boundary layers.
- Analyzed parametric sensitivity, focusing on glucose diffusion coefficients.
- Modeled the influence of a fibrotic capsule layer.
Main Results:
- External mass transfer boundary layers increased response time by 3.7-fold.
- Sensor response time is most sensitive to the glucose diffusion coefficient in the membrane.
- Model predictions were shorter than experimental data for an intensity-based sensor.
- A fibrotic capsule layer increased response time by 5-fold.
Conclusions:
- Mathematical modeling provides insights into optical glucose sensor kinetics.
- Diffusion limitations and in vivo encapsulation significantly impact sensor response time.
- Further model refinement is needed to match experimental observations.
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