未成熟秋葵(Abelmoschus Esculentus)果实与成熟秋葵(Abelmoschus Esculentus)果实抗氧化特性的相关性

Miza Badriah Nazri, Azrina Azlan, Sharmin Sultana, Rozita Yahya
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引用次数: 0

摘要

本研究旨在评估和比较成熟秋葵和未成熟秋葵的抗氧化活性和含量(总黄酮含量和总酚含量)。研究采用四种方法对秋葵果实的抗氧化活性进行了检测,即氯化铝比色法、Folin-Ciocalteu 法、1, 1-二苯基-2-苦基肼(DPPH)法和还原抗氧化力(FRAP)法。未成熟、成熟和非常成熟的秋葵样品(分别为 8 天以下、10-15 天和 20 天以上)使用两种不同的溶剂(65% 乙醇和水)进行提取。用成熟乙醇提取的样品总酚含量(TPC)最高,为 21.564 ± 1.635 mg GAE/g,而用极成熟乙醇提取的样品总酚类化合物(TFC)最高,为 54.391 ± 8.224 mg QE/g。成熟的 65% 乙醇提取样品的 DPPH 清除活性 IC50 值最低(0.920± 0.096 mg/ml),成熟的乙醇提取样品的 FRAP 值最高(232.018± 5.337 μmol Fe2+/g)。这些研究表明,成熟秋葵乙醇提取物的抗氧化剂含量和活性均高于秋葵水提取物。根据 DPPH 自由基清除试验,TPC(r = 0.860)、TFC(r = 0.742)与 FRAP 评估的抗氧化活性之间存在良好的关联,表明酚类和类黄酮对提取物的抗氧化特性都有贡献。TPC和TFC与IC50值均呈负相关(r = -0.766,r = -0.650)。总之,用 65% 乙醇提取的成熟秋葵果实的抗氧化剂含量高于秋葵果实的水提取物,可作为抗氧化剂的来源而不是丢弃。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Correlation of Antioxidant Properties Between Immature and Mature Okra (Abelmoschus Esculentus) Fruits
This study aimed to assess and compare the antioxidant activity and content (total flavonoid levels and total phenolic) of mature and immature okra. The antioxidant activity of okra fruits was assayed using four methods, namely: Aluminium Chloride Colorimetric assay, Folin-Ciocalteu assay, 1, 1-diphenyl-2-picrylhydrazyl (DPPH), and Reducing Antioxidant Power assay (FRAP) assays. The immature, mature, and very mature okra samples (less than 8 days, 10-15 days, and more than 20 days, respectively) were extracted using two different solvents (65% ethanol and water). The sample that was extracted with mature ethanol had the highest Total Phenolic Content (TPC) at 21.564 ± 1.635 mg GAE/g, while the sample that was extracted with extremely mature ethanol had the highest TFC at 54.391 ± 8.224 mg QE/g. The mature 65% ethanolic extracted sample showed the lowest IC50 value of DPPH scavenging activity (0.920± 0.096 mg/ml), and the mature ethanol extracted sample had the highest FRAP value (232.018± 5.337 μmol Fe2+/g). These studies showed that ethanolic extracts of mature Abelmoschus esculentus had higher antioxidant content and activity than okra water extracts. Based on the DPPH Radical Scavenging Assay revealed favourable associations between TPC (r = 0.860), TFC (r = 0.742), and antioxidant activity as evaluated by FRAP, demonstrating that both phenolics and flavonoids contributed to the extract’s antioxidant properties. Both TPC and TFC showed negative correlations with IC50 values (r = -0.766, r = -0.650, respectively). In conclusion, the mature okra fruits extracted with 65% ethanol give higher antioxidant content than the water extracts of okra fruits and potentially be used as a source of antioxidants rather than be discarded.
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