: This work presents a spectrophotometric method for the determination of indole-3-carbaldehyde (I3A), a bioactive metabolite of tryptophan, in white cauliflower (Brassica oleracea L. var. botrytis). The colorimetric assay is based on the self-condensation of I3A under acidic conditions, forming di-indolylmethine salt (urorosein). The absorbance of urorosein at 490 nm was used for I3A quantification with a microplate reader. Key parameters, including acidity, solvent composition, temperature, and reaction time, were optimized to achieve the best analytical performance. This method exhibited a linear dynamic range up to 100 μM with excellent repeatability (avRSD 1.7 %) and a high coefficient of determination (R2 0.9975). The limit of detection and quantification were 0.469 ± 0.007 μM and 1.562 ± 0.023 μM, respectively. As proof of concept, the assay was applied to white cauliflower extract, achieving a 113 % recovery compared to LC-MS analysis. This method potentially offers a simple approach for the detection of I3A in foods.

Colorimetric detection of indole-3-carbaldehyde in white cauliflower by self-condensation reaction giving urorosein / Palladino, Pasquale; Muscatello, Beatrice; Minunni, Maria. - In: TALANTA. - ISSN 0039-9140. - ELETTRONICO. - 294:(2025), pp. 128238.1-128238.9. [10.1016/j.talanta.2025.128238]

Colorimetric detection of indole-3-carbaldehyde in white cauliflower by self-condensation reaction giving urorosein

Palladino, Pasquale
;
Minunni, Maria
2025

Abstract

: This work presents a spectrophotometric method for the determination of indole-3-carbaldehyde (I3A), a bioactive metabolite of tryptophan, in white cauliflower (Brassica oleracea L. var. botrytis). The colorimetric assay is based on the self-condensation of I3A under acidic conditions, forming di-indolylmethine salt (urorosein). The absorbance of urorosein at 490 nm was used for I3A quantification with a microplate reader. Key parameters, including acidity, solvent composition, temperature, and reaction time, were optimized to achieve the best analytical performance. This method exhibited a linear dynamic range up to 100 μM with excellent repeatability (avRSD 1.7 %) and a high coefficient of determination (R2 0.9975). The limit of detection and quantification were 0.469 ± 0.007 μM and 1.562 ± 0.023 μM, respectively. As proof of concept, the assay was applied to white cauliflower extract, achieving a 113 % recovery compared to LC-MS analysis. This method potentially offers a simple approach for the detection of I3A in foods.
2025
294
1
9
Palladino, Pasquale; Muscatello, Beatrice; Minunni, Maria
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Utilizza questo identificatore per citare o creare un link a questa risorsa: https://hdl.handle.net/2158/1421400
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