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采用分析化学-化学计量学联用方法,通过模拟胃肠道消化,体外测定多酚生物利用度。

A combined analytical-chemometric approach for the in vitro determination of polyphenol bioaccessibility by simulated gastrointestinal digestion.

机构信息

Analytical Chemistry Department, Faculty of Chemistry, Complutense University of Madrid, 28040, Madrid, Spain.

出版信息

Anal Bioanal Chem. 2022 Mar;414(8):2739-2755. doi: 10.1007/s00216-022-03922-x. Epub 2022 Feb 2.

Abstract

In this study, an integrated characterisation through polyphenol and caffeine content and antioxidant activity was combined with chemometric analysis to assess the effects of simulated in vitro gastrointestinal digestion on the bioaccessibility of these bioactive compounds from nine different tea infusions. Tea infusions were characterised based on total flavonoids, total polyphenols and antioxidant activity, together with the determination of individual polyphenol content. Fourteen phenolic compounds, including phenolic acids, stilbenes and flavonoids, were selected based on their reported bioactivity and high accessibility, attributed to their low molecular weight. Both polyphenols and caffeine were initially monitored in raw tea infusions and through the different digestion stages (salivary, gastric and duodenal) by capillary high performance liquid chromatography coupled to diode array detection (cHPLC-DAD) and/or HPLC coupled to a triple quadrupole mass analyser (HPLC-MS/MS). Multivariate analysis of the studied bioactives, using principal component analysis and cluster analysis, revealed that the decaffeination process seems to increase the stability and concentration of the compounds evaluated during digestion. The greatest transformations occurred mainly in the gastric and duodenal stages, where low bioactivity indices (IVBA) were shown for resveratrol and caffeic acid (IVBA = 0%). In contrast, the polyphenols gallic acid, chlorogenic acid and quercetin gave rise to their availability in white, green and oolong infusion teas (IVBA > 90%). Furthermore, highly fermented black and pu-erh varieties could be designated as less bioaccessible environments in the duodenum with respect to the tested compounds.

摘要

在这项研究中,通过多酚和咖啡因含量以及抗氧化活性的综合特征,并结合化学计量分析,评估了模拟体外胃肠道消化对来自 9 种不同茶浸提液中这些生物活性化合物生物利用度的影响。茶浸提液的特征基于总类黄酮、总多酚和抗氧化活性,以及对单体多酚含量的测定。根据其报道的生物活性和高可及性,选择了 14 种酚类化合物,包括酚酸、芪类和类黄酮,因为它们的分子量较低。多酚和咖啡因最初通过毛细管高效液相色谱与二极管阵列检测(cHPLC-DAD)和/或高效液相色谱与三重四极杆质谱联用(HPLC-MS/MS)在原始茶浸液以及不同消化阶段(唾液、胃和十二指肠)中进行监测。使用主成分分析和聚类分析对研究生物活性进行多元分析,结果表明脱咖啡因过程似乎增加了消化过程中评估化合物的稳定性和浓度。最大的转化主要发生在胃和十二指肠阶段,其中白藜芦醇和咖啡酸的生物活性指数(IVBA)较低(IVBA=0%)。相比之下,多酚没食子酸、绿原酸和槲皮素在白茶、绿茶和乌龙茶浸提液中产生了其可用性(IVBA>90%)。此外,与测试化合物相比,高度发酵的黑茶和普洱品种在十二指肠中可被指定为生物利用度较低的环境。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9dc2/8888401/e010dc8da54b/216_2022_3922_Fig1_HTML.jpg

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