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Highly thiolated corn starch for enhanced mucoadhesion and permeation
Zahra Davoudi1, Gergely Kali2, Doris Braun2
1Department of Pharmaceutical Technology, University of Innsbruck, Institute of Pharmacy, Center for Chemistry and Biomedicine, Innrain 80-82, 6020 Innsbruck, Austria; Department of Food Science and Technology, Faculty of Agriculture, Tarbiat Modares University, Tehran, Iran.
Highly thiolated corn starch enhances drug delivery by improving mucoadhesion and permeation. This modified starch shows no cytotoxicity, making it a promising excipient for mucosal applications.
Area of Science:
- Materials Science
- Pharmaceutical Sciences
- Biotechnology
Background:
- Developing novel excipients is crucial for effective mucosal drug delivery.
- Corn starch is an abundant and biocompatible polysaccharide.
- Thiolation can modify starch properties for enhanced functionality.
Purpose of the Study:
- To synthesize and characterize highly thiolated corn starch.
- To evaluate its mucoadhesive and permeation enhancing properties.
- To assess its potential as an excipient for mucosal drug delivery.
Main Methods:
- Chemical thiolation of native corn starch using phosphorous pentasulfide.
- Characterization using Ellman's test, 1H NMR, FTIR, and DSC.
- Cytotoxicity assessment via resazurin viability assay.
- Evaluation of swelling, viscosity, mucoadhesion (rheology, tensile testing), and permeation (using sodium fluorescein).
Main Results:
- Thiolated starch (1658 μmol/g thiol groups) exhibited no cytotoxicity at 0.2 mg/ml.
- A 3.5-fold increase in dynamic viscosity and a 91.1-fold enhancement in mucoadhesion were observed.
- Tensile testing showed a 4.3-fold increase in detachment force.
- A 2-fold increase in permeation enhancement of sodium fluorescein across rat intestinal mucosa was demonstrated.
Conclusions:
- Highly thiolated corn starch possesses significant mucoadhesive and permeation enhancing capabilities.
- The modified starch demonstrates good safety profile.
- It represents a promising excipient for advancing mucosal drug delivery systems.
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