Caffeoylquinic acids (CQAs) are nutraceutical polyphenols highly represented in natural sources, including artichoke waste (AW). In this study a colorimetric method for rapid and sustainable detection of a 5-CQA isomer (Chlorogenic acid) in AW extract was developed by using alkaline Tris buffer (10 mmol L−1, pH 9) to generate a yellow color associated with 5- to 3-CQA isomerization reaction, as suggested by NMR and MS analyses. The strong absorbance at 360 nm was followed by standard UV–Vis methodology. The colorimetric assay was exploited for detection of 5-CQA into leaf extract from artichoke, obtaining a value of 15.2 ± 0.3 μg/mg of dry extract, in agreement with HPLC analysis (14.3 ± 0.7 μg/mg, 106 ± 2 % recovery) used as validation technique, with excellent linear correlation and precision (R2 = 0.9996, avRSD% = 3.2 %). The method is fast and selective, offering a valuable tool for nutraceuticals identification and food waste valorization.
Fast, sensitive, and sustainable colorimetric detection of chlorogenic acid in artichoke waste material / Cuffaro, Doretta; Palladino, Pasquale; Digiacomo, Maria; Bertini, Simone; Minunni, Maria; Macchia, Marco. - In: FOOD CHEMISTRY. - ISSN 0308-8146. - ELETTRONICO. - 463:(2025), pp. 141505.1-141505.7. [10.1016/j.foodchem.2024.141505]
Fast, sensitive, and sustainable colorimetric detection of chlorogenic acid in artichoke waste material
Palladino, Pasquale
;Bertini, Simone;Minunni, Maria;
2025
Abstract
Caffeoylquinic acids (CQAs) are nutraceutical polyphenols highly represented in natural sources, including artichoke waste (AW). In this study a colorimetric method for rapid and sustainable detection of a 5-CQA isomer (Chlorogenic acid) in AW extract was developed by using alkaline Tris buffer (10 mmol L−1, pH 9) to generate a yellow color associated with 5- to 3-CQA isomerization reaction, as suggested by NMR and MS analyses. The strong absorbance at 360 nm was followed by standard UV–Vis methodology. The colorimetric assay was exploited for detection of 5-CQA into leaf extract from artichoke, obtaining a value of 15.2 ± 0.3 μg/mg of dry extract, in agreement with HPLC analysis (14.3 ± 0.7 μg/mg, 106 ± 2 % recovery) used as validation technique, with excellent linear correlation and precision (R2 = 0.9996, avRSD% = 3.2 %). The method is fast and selective, offering a valuable tool for nutraceuticals identification and food waste valorization.File | Dimensione | Formato | |
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