Flavonoids quantification in Acer negundo L., extracts by hplc analysis

##plugins.themes.bootstrap3.article.main##

Rafael Salgado-Garciglia https://orcid.org/0000-0001-5920-6562
Alejandra Hernández-García https://orcid.org/0000-0001-8353-0266
Jorge Montiel-Montoya https://orcid.org/0000-0002-4089-8033
Maribel Valdez-Morales https://orcid.org/0000-0002-6812-5905
Luis Germán López-Valdez https://orcid.org/0000-0002-3238-5035
Braulio Edgar Herrera-Cabrera https://orcid.org/0000-0001-9670-8721
Fabiola Zaragoza-Martínez https://orcid.org/0000-0002-6341-7028
Gonzalo Guillermo Lucho Constantino https://orcid.org/0000-0002-2857-8352
HEBERT JAIR BARRALES-CUREÑO

Keywords

ferulic acid, gentisic acid, flavonoids, HPLC.

Resumen

Objective: The identify and quantify, by high performance liquid chromatography,Nflavonoids from leaf and stem extracts of Acer negundo.
Design/methodology/approach: Ethanolic extracts of Acer negundo were analysed with high performance liquid chromatography to quantify and identify their major antioxidant flavonoids.
Results: Leaf extracts had high concentrations of rutin (34.19 µg/mL) and catechin (33.97 µg/mL), intermediate concentrations of apigenin (19.05 µg/mL), gallic acid (19.04 µg/mL), ferulic acid (17.2 µg/mL) and 2.5 dihydroxybenzoic acid (12.72 µg/mL), and low concentrations of caffeic acid (6.15 µg/mL), quercetin-3-β-glucoside (4.97 µg/mL) and isorhamnetin (4.68 µg/mL). In the stem´s extracts, the highest concentrations were of ferulic acid (7.96 µg/mL), rutin (5.61 µg/mL) and catechin (4.37 µg/mL); medium concentration were identified for isorhamnetin (3.31 µg/mL) and quercetin-3-β-glucoside (2.01 µg/mL) and apigenin (0.79 µg/mL) was identified at the low concentrations. Gallic acid, caffeic acid or 2,5-dihydroxybenzoic acid were not detected.
Limitations/implications: Some flavonoids have been identified in other Acer species but have not been identified and quantified in Acer negundo, a Mexicanspecies.
Findings/conclusions: For the first time we report gentisic acid in Acer negundo leaf extracts. This analytical method can be standardized to serve as a qualityanalysis of maple tree products.

Abstract 417 | EARLY ACCESS 8 Downloads 0