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Electrophoretic Crystallization of Ultrathin High-performance Metal-organic Framework Membranes
Published on: August 16, 2018
Diffusional properties of zein membranes and matrices
Yoon K Oh1, Douglas R Flanagan
1Division of Pharmaceutics, College of Pharmacy, University of Iowa, Iowa City, Iowa 52242, USA. yoon.k.oh@gsk.com
Drug Development and Industrial Pharmacy
|October 24, 2009
Summary
Zein protein forms aqueous channels upon hydration, influencing drug diffusion. These channels, dependent on permeant solubility and matrix properties, are key to controlled release formulations.
Area of Science:
- Biomaterials Science
- Pharmaceutical Technology
- Polymer Science
Background:
- Zein, a hydrophobic corn protein, is explored for biodegradable pharmaceutical applications.
- Previous studies indicated zein's swelling behavior impacts permeation.
- Understanding zein's diffusion properties is crucial for controlled release systems.
Purpose of the Study:
- To investigate the diffusional behavior of model drugs in zein systems.
- To characterize diffusional parameters like effective diffusion coefficients, porosity, and tortuosity.
- To propose an alternative method for calculating porosity and tortuosity.
Main Methods:
- Analysis of drug release and membrane diffusion profiles.
- Calculation of effective diffusion coefficients, porosities, and tortuosities.
- Experimental investigation of zein matrices and membranes.
Main Results:
- Zein systems exhibit diffusion primarily through aqueous channels formed during hydration and swelling.
- Drug permeation and release are influenced by permeant solubility and matrix/membrane permeability.
- Calculated parameters support the proposed aqueous channel model for zein diffusion.
Conclusions:
- Zein matrices and membranes hydrate and swell, creating dominant aqueous diffusional pathways.
- The findings support the aqueous channel model for understanding drug diffusion through zein.
- Zein's properties make it a promising material for controlled drug delivery systems.
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