ArticleJournal of fluorescence2026
Chiral Ratiometric Fluorescent Silicon Nanoparticles for "Turn-on" Enantioselective Recognition of Tryptophan.
Article in Journal of fluorescence, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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Abstract
This study presents a novel ratiometric fluorescent silicon nanoparticles (LSiNPs) system for enantioselective recognition of tryptophan. The LSiNPs were synthesized by DAMO, rhodamine B and chiral ligand L-Lys via a one-pot method at room temperature. Upon increasing L-Trp concentration, the fluorescence intensity of the system at 440 nm progressively enhanced while maintaining stability at 575 nm, whereas D-Trp showed negligible effects. The sensor demonstrated an enantioselectivity coefficient of 11.7, enabling quantitative detection of L-Trp and determining enantiomeric composition in racemic mixtures. LSiNPs exhibits good selectivity towards L-Trp among 13 typical amino acid enantiomers. It can be applied to detect L-Trp in L-Tryptophan capsules rapidly and accurately. The recognition mechanism of tryptophan enantiomers was studied, indicating that the modification of chiral ligand L-Lys plays an important role in the recognition process. This work establishes a “turn-on” ratiometric strategy for chiral recognition of tryptophan enantiomers, offering new perspectives for enantiomer differentiation.
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