Smart Quercetin Delivery: Tailored Sodium Alginate Microbeads for Enhanced Antioxidant and Controlled Degradation
Keywords:
sodium alginate, quercetin, drug delivery, antioxidant, degradationAbstract
Quercetin (Qur), a natural flavonoid exhibiting significant antioxidant, anti-inflammatory, and anti-cancer effects, encounters constraints in clinical use owing to inadequate solubility, diminished bioavailability, and fast metabolism. To address these problems, sodium alginate (Na-Algn), which is biocompatible and biodegradable, has emerged as a viable medium for Qur delivery. This study aims to design and optimize the Qur-loaded Na-Ag microbead carriers, examining the impact of different calcium chloride concentrations on cross-linking density and release patterns of the therapeutic agent. Change of cross-linker and Na-Algn alters the drug encapsulation efficiency (EE %). This approach improves the bioavailability of quercetin (Qur) and stability by utilizing the interaction between Qur, calcium ions, and the alginate matrix, hence extending its therapeutic effects. The degradation, morphological, antioxidant, and in vitro drug release findings indicate that Na-Algn beads serve as versatile and effective vehicles for drug administration, positioning them as attractive options for enhancing the clinical efficacy of bioactive therapeutic agents
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Copyright (c) 2025 K. Abinaashree, H. Thamizhchelvan, Jayalakshmi Somasundaram, Radha Gosala (Author)

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