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◆ Food Chemistry2026-02-04· Chemistry

Structure-activity relationships of red cabbage anthocyanins from AAPH reactivity using HPLC-HRMS/MS and electrochemical detector

Claudia Lombroni, Lucrezia Angeli, Matteo Scampicchio, Giovanna Ferrentino, Ksenia Morozova

原始摘要(英文原文)· Original abstract
The antioxidant activity of anthocyanins in red cabbage ( Brassica oleracea var. capitata f. rubra ) was evaluated using a multi-method approach combining kinetic, chromatographic, and electrochemical techniques. While numerous studies have examined anthocyanin antioxidant activity using isolated assays, few have integrated kinetic measurements with electrochemical profiling. High-resolution HPLC-MS/MS enabled the identification and quantification of thirteen cyanidin-based derivatives, predominantly acylated with sinapic, ferulic, or p -coumaric acids. The radical-scavenging capacity was evaluated using a stopped-flow DPPH kinetic assay and a degradation protocol employing the radical initiator 2,2′-azodiisobutyramidine dihydrochloride (AAPH). Among the characterized compounds, cyanidin-3-(disinapoyl)-diglucoside-5-glucoside (Cy3(disin)diG5G) exhibited the highest degradation rate, possibly due to the presence of two sinapoyl moieties. Electrochemical profiling by HPLC-DAD-CAD showed that compounds with lower half-wave potentials (E 1/2 ) displayed greater reactivity. Cy3(disin)diG5G exhibited the lowest E 1/2 (+525 mV), confirming it as a highly reactive antioxidant. These findings suggest that structural features such as acylation and glycosylation, alter both the redox potential and degradation kinetics, which may contribute to a deeper understanding of the structure–activity relationships in polyphenolic antioxidants in food. The present work, with the integration of kinetic measurements and electrochemical profiling, could provide a more mechanistic and realistic assessment of antioxidant function in complex food matrices. • 13 cyanidin derivatives were identified & quantified in red cabbage via HPLC-HRMS/MS. • Acylation/glycosylation strongly affected anthocyanin degradation rates. • Cy3(disin)diG5G showed the highest reactivity and lowest half-wave potential (E 1/2 ). • Electrochemical analysis confirmed the results obtained with HRMS. • The two methods showed a strong correlation.
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Structure-activity relationships of red cabbage anthocyanins from AAPH reactivity using HPLC-HRMS/MS and electrochemical detector — 科研速览 Science Skim