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Natrium Alginate and Graphene Nanoplatelets-Based Efficient Material for Resveratrol Delivery
Cristina Mormile1,2,3, Ocsana Opriș1, Stefano Bellucci2,4
1National Institute for Research and Development of Isotopic and Molecular Technologies, 67-103 Donat, 400293 Cluj-Napoca, Romania.
Graphene-enhanced alginate beads improve resveratrol drug delivery. These biocompatible composite beads show controlled, pH-dependent release, offering potential for therapeutic applications.
Area of Science:
- Biomaterials Science
- Drug Delivery Systems
- Nanotechnology
Background:
- Resveratrol possesses therapeutic potential but requires effective delivery systems.
- Alginate hydrogels are widely used for drug encapsulation.
- Controlled release mechanisms are crucial for optimizing therapeutic efficacy.
Purpose of the Study:
- To develop alginate-based composite beads for resveratrol delivery.
- To investigate the effect of graphene nanoplatelets on resveratrol release kinetics.
- To evaluate the biocompatibility of the developed drug delivery system.
Main Methods:
- Fabrication of alginate-resveratrol (AR) and alginate-graphene-resveratrol (AGR) beads via ionic cross-linking.
- Characterization of bead formation and resveratrol encapsulation.
- In vitro release studies of resveratrol from beads in phosphate-buffered saline at varying pH.
- Kinetic analysis of drug release profiles.
- Cytotoxicity assessment using normal human cells.
Main Results:
- Graphene incorporation in AGR beads enhanced resveratrol release, particularly at pH 6.8, suggesting a pH-driven release.
- The Higuchi model accurately described the resveratrol release mechanism from the beads.
- Cytotoxicity tests confirmed the biocompatibility of the graphene-enhanced alginate system with normal human cells.
Conclusions:
- Graphene-enhanced alginate matrices are effective for controlled resveratrol delivery.
- The developed system demonstrates pH-dependent release characteristics.
- These findings highlight the potential of graphene-alginate composites for advanced drug delivery applications.
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