Abstract
Chitosan-pectin membranes are biodegradable polyelectrolyte complexes, derived from biomaterials, with good stability for drug delivery applications. This study investigates the potential of these membranes to encapsulate quercetin, a flavonoid known for its therapeutic properties but limited for its low solubility, poor bioavailability, and rapid elimination. The membranes were synthesized using a 1:1 (w/w) chitosan-to-pectin ratio and loaded with quercetin via solvent evaporation. Characterization using FTIR confirmed the presence of OH, C=O, and NH groups; XRD indicated semi-crystalline structure; and SEM revealed a uniform, porous morphology. The maximum quercetin loading efficiency reached 82.43%, with the highest release (90.39%) observed at pH 1.2, following first-order kinetics. The resulting membrane was thin, brown, homogeneous, and tear-resistant, demonstrating its potential as a controlled drug delivery matrix for quercetin
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CITATION STYLE
Hastuti, B., Hadi, S., Nisriyah, S., Martanisa, M., & Kamari, A. (2025). Quercetin Encapsulation on Chitosan-Pectin Membranes as a Drug Delivery and Its Release Kinetics. Jurnal Sains Materi Indonesia, 27(1), 37–43. https://doi.org/10.55981/jsmi.2025.9988
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