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Electrosprayed Alginate-Fmoc Amino Acid Microcapsules for Quercetin Loading and Release
Hatice Asri1, Serap Mert2,3,4
1Department of Biomedical Engineering, Faculty of Technology, Kocaeli University, 41001 Kocaeli, Türkiye.
ACS Omega
|July 3, 2026
Summary
Hybrid microcapsules incorporating Fmoc-amino acids into alginate demonstrate enhanced structural durability and prolonged quercetin release compared to standard Ca-Alginate microcapsules. These advanced formulations offer improved drug delivery performance and stability.
Area of Science:
- Materials Science
- Biomedical Engineering
- Drug Delivery
Background:
- Alginate microcapsules are widely used for drug delivery.
- Enhancing the structural integrity and release profile of alginate microcapsules is crucial for effective drug delivery.
- Quercetin is a bioactive compound with therapeutic potential, requiring suitable delivery systems.
Purpose of the Study:
- To develop and characterize novel hybrid microcapsules by incorporating Fmoc-Tyrosine (Fmoc-Y) or Fmoc-Proline (Fmoc-Pro) into alginate.
- To evaluate the impact of these hybrid structures on quercetin loading, release kinetics, and swelling properties.
- To assess the structural stability and morphological changes of the microcapsules under different pH conditions.
Main Methods:
- Hybrid microcapsules were synthesized by incorporating Fmoc-Y or Fmoc-Pro into alginate, followed by Ca2+-ion cross-linking.
- Characterization included particle size analysis, Fourier-transform infrared spectroscopy (FTIR), rheological studies, and scanning electron microscopy (SEM).
- Quercetin release profiles and microcapsule swelling behavior were investigated at pH 7.4 and pH 1.2, respectively.
Main Results:
- Hybrid microcapsules (Ca-Alginate/Fmoc-Y and Ca-Alginate/Fmoc-Pro) exhibited smaller particle sizes (154 ± 14 μm and 131 ± 15 μm) compared to pure Ca-Alginate (187 ± 19 μm).
- FTIR confirmed the successful incorporation of Fmoc-amino acids into the alginate matrix.
- Quercetin release at pH 7.4 was significantly prolonged in hybrid microcapsules (up to 24 h) compared to pure alginate (7 h), following Korsmeyer-Peppas and zero-order models, respectively.
- Hybrid microcapsules demonstrated superior structural stability and reduced erosion at pH 7.4 (stable up to 16 h) compared to pure alginate microcapsules (eroded by 6 h).
- SEM analysis revealed a more compact and less porous surface morphology for hybrid microcapsules.
Conclusions:
- The incorporation of Fmoc-Y and Fmoc-Pro into alginate significantly enhances the structural durability and controlled release of quercetin from microcapsules.
- Hybrid microcapsules offer improved performance for drug delivery applications, maintaining integrity over extended periods and controlled release profiles.
- These findings highlight the potential of Fmoc-amino acid-modified alginate as a promising platform for advanced drug delivery systems.
