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山楂叶作为生物活性化合物的潜在来源:提取优化与提取物表征

Haw. Leaves as a Potential Source of Bioactive Compounds: Extraction Optimization and Extract Characterization.

作者信息

Bermúdez-Bazán Misael, Estarrón-Espinosa Mirna, Castillo-Herrera Gustavo Adolfo, Escobedo-Reyes Antonio, Urias-Silvas Judith Esmeralda, Lugo-Cervantes Eugenia, Gschaedler-Mathis Anne

机构信息

Centro de Investigación y Asistencia en Tecnología y Diseño del Estado de Jalisco, A.C., Unidad de Tecnología Alimentaria, Camino Arenero 1227, El Bajío, Zapopan 45019, Jalisco, Mexico.

Centro de Investigación y Asistencia en Tecnología y Diseño del Estado de Jalisco, A.C., Unidad de Servicios Analíticos y Metrológicos, Av. Normalistas No. 800, Guadalajara 44270, Jalisco, Mexico.

出版信息

Molecules. 2024 Mar 3;29(5):1137. doi: 10.3390/molecules29051137.

DOI:10.3390/molecules29051137
PMID:38474649
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10935067/
Abstract

The leaves of Haw. are the main agro-waste generated by the mezcal industry and are becoming an important source of bioactive compounds, such as phenolic compounds, that could be used in the food and pharmaceutical industries. Therefore, the extraction and identification of these phytochemicals would revalorize these leaf by-products. Herein, maceration and supercritical carbon dioxide (scCO) extractions were optimized to maximize the phenolic and flavonoid contents and the antioxidant capacity of vegetal extracts of Haw. In the maceration process, the optimal extraction condition was a water-ethanol mixture (63:37% /), which yielded a total phenolic and flavonoid content of 27.92 ± 0.90 mg EAG/g DL and 12.85 ± 0.53 µg QE/g DL, respectively, and an antioxidant capacity of 32.67 ± 0.91 (ABTS assay), 17.30 ± 0.36 (DPPH assay), and 13.92 ± 0.78 (FRAP assay) µM TE/g DL. Using supercritical extraction, the optimal conditions for polyphenol recovery were 60 °C, 320 bar, and 10% /. It was also observed that lower proportions of cosolvent decreased the polyphenol extraction more than pressure and temperature. In both optimized extracts, a total of 29 glycosylated flavonoid derivatives were identified using LC-ESI-QTof/MS. In addition, another eight novel compounds were identified in the supercritical extracts, showing the efficiency of the cosolvent for recovering new flavonoid derivatives.

摘要

龙舌兰的叶子是梅斯卡尔酒业产生的主要农业废弃物,正成为生物活性化合物(如酚类化合物)的重要来源,这些化合物可用于食品和制药行业。因此,提取和鉴定这些植物化学物质将使这些叶子副产品更具价值。在此,对浸渍法和超临界二氧化碳(scCO)萃取法进行了优化,以最大限度地提高龙舌兰植物提取物的酚类和黄酮类含量以及抗氧化能力。在浸渍过程中,最佳提取条件是水 - 乙醇混合物(63:37% /),其总酚和黄酮含量分别为27.92±0.90 mg EAG/g DL和12.85±0.53 µg QE/g DL,抗氧化能力分别为32.67±0.91(ABTS法)、17.30±0.36(DPPH法)和13.92±0.78(FRAP法)µM TE/g DL。采用超临界萃取时,多酚回收的最佳条件是60℃、320 bar和10% /。还观察到,与压力和温度相比,较低比例的共溶剂对多酚萃取的降低作用更大。在两种优化提取物中,使用LC - ESI - QTof/MS共鉴定出29种糖基化黄酮衍生物。此外,在超临界提取物中还鉴定出另外8种新化合物,表明共溶剂在回收新黄酮衍生物方面的效率。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d8cf/10935067/49fd9e8bbb4c/molecules-29-01137-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d8cf/10935067/aba69ac40df6/molecules-29-01137-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d8cf/10935067/97f6c4cef51d/molecules-29-01137-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d8cf/10935067/aa279878910a/molecules-29-01137-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d8cf/10935067/b655c360990b/molecules-29-01137-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d8cf/10935067/d6b8c9848363/molecules-29-01137-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d8cf/10935067/01858a548863/molecules-29-01137-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d8cf/10935067/9c2431d21a59/molecules-29-01137-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d8cf/10935067/49fd9e8bbb4c/molecules-29-01137-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d8cf/10935067/aba69ac40df6/molecules-29-01137-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d8cf/10935067/97f6c4cef51d/molecules-29-01137-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d8cf/10935067/aa279878910a/molecules-29-01137-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d8cf/10935067/b655c360990b/molecules-29-01137-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d8cf/10935067/d6b8c9848363/molecules-29-01137-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d8cf/10935067/01858a548863/molecules-29-01137-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d8cf/10935067/9c2431d21a59/molecules-29-01137-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d8cf/10935067/49fd9e8bbb4c/molecules-29-01137-g008.jpg

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