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Efecto del líquido iónico a base de colina-triptófano en la solubilidad y la actividad de eliminación de la
Vibek Srichandan1, Malabika Talukdar2, Sanghamitra Pradhan3
1Department of Chemistry, Faculty of Engineering and Technology (ITER), Siksha 'O' Anusandhan, Deemed to be University), Bhubaneswar, 751030, Odisha, India.
Abstract:
The limited aqueous solubility of quercetin severely restricts its bioavailability and functional applications. This study demonstrates the effectiveness of a biocompatible choline-tryptophan ionic liquid ([Ch][Trp]) IL in enhancing the solubility and antioxidant performance of quercetin. Incorporation into the IL medium produced a concentration-dependent modulation of 2,2-diphenyl-1-picrylhydrazyl (DPPH•) radical scavenging activity, with the highest IL concentration (0.18 mM) increasing RSA from 74.76% (quercetin alone) to 78.18%, whereas lower IL concentrations resulted in slightly reduced activity. Physicochemical evaluation of quercetin-[Ch][Trp]-water solutions revealed structure-making behaviour, reflected by a positive Hepler constant and negative Sv values, indicating strengthened water structuring and weak ion-ion interactions conducive to solute stabilization. Spectroscopic analyses supported these findings: UV-Vis absorption exhibited a red shift, fluorescence intensity increased, and FTIR spectra confirmed specific hydrogen-bonding and π-π interactions between quercetin and the IL. Collectively, these results show that [Ch][Trp] creates a favourable micro structured environment that stabilizes quercetin, modulates its radical-scavenging performance, and improves its physicochemical properties. This work highlights the potential of amino-acid-based ILs as green, multifunctional media for improving the performance of poorly water-soluble bioactive compounds.
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