两种不同提取方法对肝硬化红宝石提取物的植物化学成分、抗氧化和抗菌活性的影响

Emna Chaabani, Iness Bettaieb Rebey, Wissem Aidi Wannes, Riadh Ksouri, Abdessalem Shili
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Results: The successive extraction of R. cirrhosa extract relatively showed higher total phenol (38.1 mg GAE/g) and condensed tannin (18.07 mg CE/g) contents than the maceration extraction (35.43 mg EAG/g and 12.99 mg CE/g, respectively). However, the total flavonoid amount of RCE was higher in the maceration extraction (33.09 mg CE/g) than in the successive extraction (21.27 mg CE/g). The total antioxidant capacity of RCE indicated a decrease in this activity after fractionation. Indeed, the activity of RCE decreased from 47.8 to 37.83 mg GAE/g, and RCE obtained by the two extraction methods showed moderate antioxidant activity using reducing power (IC50=380-490 µg/mL) and β-carotene bleaching (IC50=110-310 μg/mL) assays. 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摘要

背景:目前,人们越来越关注从海洋中发现新的生物活性物质。本研究旨在通过两种不同的提取方法对突尼斯芦皮肝硬化提取物(RCEs)的植物化学成分及其抗氧化和抗菌活性进行表征。方法:采用浸渍和连续提取两种不同的提取方法获得rce。用量热法测定其多酚含量和抗氧化活性,并用固体扩散法观察其对致病菌和真菌的抑制作用。结果:连续提取的肝硬化硬皮炎提取物总酚(38.1 mg GAE/g)和缩合单宁(18.07 mg CE/g)含量相对高于浸渍提取的(35.43 mg EAG/g和12.99 mg CE/g)。浸渍法提取的黄芪总黄酮含量为33.09 mg CE/g,高于连续法提取的21.27 mg CE/g。RCE的总抗氧化能力在分离后呈下降趋势。RCE的活性从47.8 mg GAE/g降至37.83 mg GAE/g,通过还原力(IC50=380 ~ 490 μg/mL)和β-胡萝卜素漂白(IC50=110 ~ 310 μg/mL)测定,两种提取方法得到的RCE具有中等的抗氧化活性。除鼠伤寒沙门菌(2 mm)、粪肠球菌(6 mm)和金黄色链球菌(3.67 mm)外,浸渍法提取的RCEs对其他菌株(3.33 ~ 9.33 mm)的抑菌活性均高于连续提取法。念珠菌菌株对浸出的肝硬化肝杆菌提取物有敏感性。事实上,通过连续提取获得的肝硬化肝提取物对克鲁氏假丝酵母具有更高的抑制活性,其抑制直径为6 mm。结论:肝硬化雷公藤提取物中含有丰富的生物活性分子,具有十分广阔的生物学潜力。
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Variability on the Phytochemical Composition, Antioxidant and Antimicrobial Activities of Ruppia cirrhosa Extract Using Two Different Methods of Extraction
Background: Nowadays, there is increasing attention to the discovery of new bioactive substances from marine sources. This research aimed to characterize the phytochemical composition as well as antioxidant and antimicrobial activities of Tunisian Ruppia cirrhosa extracts (RCEs) using two different extraction methods. Methods: RCEs were obtained by two different extraction methods: maceration and successive extraction. The determination of polyphenolic contents and antioxidant activity was made by calorimetric assay, and the effect of RCE was observed against pathogenic bacteria and fungi using the solid diffusion method. Results: The successive extraction of R. cirrhosa extract relatively showed higher total phenol (38.1 mg GAE/g) and condensed tannin (18.07 mg CE/g) contents than the maceration extraction (35.43 mg EAG/g and 12.99 mg CE/g, respectively). However, the total flavonoid amount of RCE was higher in the maceration extraction (33.09 mg CE/g) than in the successive extraction (21.27 mg CE/g). The total antioxidant capacity of RCE indicated a decrease in this activity after fractionation. Indeed, the activity of RCE decreased from 47.8 to 37.83 mg GAE/g, and RCE obtained by the two extraction methods showed moderate antioxidant activity using reducing power (IC50=380-490 µg/mL) and β-carotene bleaching (IC50=110-310 μg/mL) assays. Furthermore, RCEs obtained by maceration had the greatest antibacterial activity against all tested strains (IZ=3.33-9.33 mm) except Salmonella typhimurium (IZ=2 mm), Enterococcus faecalis (IZ=6 mm), and Streptococcus aureus (3.67 mm) as compared to those obtained by successive extraction. The strains of Candida had a sensitivity for R. cirrhosa extracts obtained by maceration. Indeed, R. cirrhosa extracts obtained by successive extraction had higher inhibitory activity against Candida krusei deduced through an inhibition diameter of 6 mm. Conclusion: It can be concluded that R. cirrhosa extract is rich in bioactive molecules, and it has an extremely promising biological potential.
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