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Isolation and Partial Characterization of Bioactive Fucoxanthin from Himanthalia elongata Brown Seaweed: A TLC-Based Approach

机译:Himanthalia elongata褐海藻中生物活性岩藻黄质的分离和部分表征:基于TLC的方法

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摘要

Seaweeds are important sources of carotenoids, and numerous studies have shown the beneficial effects of these pigments on human health. In the present study, Himanthalia elongata brown seaweed was extracted with a mixture of low polarity solvents, and the crude extract was separated using analytical thin-layer chromatography (TLC). The separated compounds were tested for their potential antioxidant capacity and antimicrobial activity against Listeria monocytogenes bacteria using TLC bioautography approach. For bio-autography, the coloured band on TLC chromatogram was visualized after spraying with DPPH and triphenyl-tetrazolium chloride reagents which screen antioxidant and antimicrobial compounds, respectively, and only one active compound was screened on the TLC plate. Preliminary identification of this active compound was done by comparing its colour and R f (retention factor) value with the authentic fucoxanthin standard. Further, the active compound was purified using preparative TLC. This purified compound showed a strong antioxidant (EC50: 14.8 ± 1.27 µg/mL) and antimicrobial (inhibition zone: 10.27 mm, 25 µg compound/disc) activities, which were examined by DPPH scavenging and agar disc-diffusion bioassay, respectively. The bioactivity shown by the purified compound was almost similar to the fucoxanthin standard. The characteristic UV-visible and FT-IR spectra of the purified active compound completely matched with the standard. Hence, the main active compound in H. elongata was identified as fucoxanthin.
机译:海藻是类胡萝卜素的重要来源,许多研究表明这些色素对人体健康具有有益作用。在本研究中,用低极性溶剂的混合物提取了Himanthalia elongata棕色海藻,并使用分析薄层色谱(TLC)分离了粗提物。使用TLC生物自动扫描技术测试分离出的化合物对单核细胞增生李斯特氏菌的潜在抗氧化能力和抗菌活性。对于生物自显影,在分别用DPPH和三苯基氯化四氮唑试剂喷雾后,可以分别看到TLC色谱上的色带,这些试剂分别筛选抗氧化剂和抗菌化合物,并且在TLC板上仅筛选了一种活性化合物。将该活性化合物的颜色和R f(保留因子)值与真品岩藻黄质标准品进行比较,即可对其进行初步鉴定。此外,使用制备型TLC纯化活性化合物。此纯化的化合物显示出很强的抗氧化剂(EC50:14.8±1.27 µg / mL)和抗微生物剂(抑制区:10.27 mm,25 µg / d),分别通过DPPH清除和琼脂圆盘扩散生物测定法进行了检测。纯化的化合物显示出的生物活性几乎与岩藻黄质标准品相似。纯化的活性化合物的特征性UV可见光谱和FT-IR光谱完全符合标准。因此,鉴定出长双螺旋菌中的主要活性化合物为岩藻黄质。

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