In Vitro Bioaccessibility and Anti-Inflammatory Activity of a Chemically Characterized Allium cepa L. Extract Rich in Quercetin Derivatives Optimized by the Design of Experiments

槲皮素 化学 灯泡 黄酮醇 萃取(化学) 生物利用度 体外 食品科学 析因实验 色谱法 抗氧化剂 传统医学 生物化学 植物 生物 药理学 医学 统计 数学
作者
Hammad Ullah,Alessandro Di Minno,Cristina Santarcangelo,Ariyawan Tantipongpiradet,Marco Dacrema,Rita Di Matteo,Hesham R. El‐Seedi,Shaden A. M. Khalifa,Alessandra Baldi,Antonietta Rossi,Maria Daglia
出处
期刊:Molecules [Multidisciplinary Digital Publishing Institute]
卷期号:27 (24): 9065-9065 被引量:1
标识
DOI:10.3390/molecules27249065
摘要

Allium cepa L. is a highly consumed garden crop rich in biologically active phenolic and organosulfur compounds. This study aimed to assess the in vitro bioaccessibility and anti-inflammatory effect of a chemically characterized A. cepa extract rich in quercetin and its derivatives. Different varieties of A. cepa were studied; based on the highest total phenolic content, the "Golden" variety was selected. Its extracts, obtained from the tunicate bulb, tunic, and bulb, were subjected to determination of quercetin and its derivatives with LC-MS analysis and based on the highest total quercetin content, the tunic extract was utilized for further experiments. The extraction method was optimized through a design of experiment (DoE) method via full factorial design, which showed that 40% ethanol and 1 g tunic/20 mL solvent are the best extraction conditions. HPLC analysis of the optimized tunic extract identified 14 flavonols, including 10 quercetin derivatives. As far as in vitro bioaccessibility was concerned, the increases in some quercetin derivatives following the gastro-duodenal digestion process support the bioaccessibility of these bioactive compounds. Moreover, the extract significantly inhibited the production of PGE2 in stimulated J774 cell lines, while no effects of the tunic extract were observed against the release of IL-1β, TNF-α, and nitrites. The study provided insights into the optimized extraction conditions to obtain an A. cepa tunic extract rich in bioavailable quercetin derivatives with significant anti-inflammatory effects against PGE2.
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