药用植物紫金菊的化学成分表征及抗氧化、抗菌和细胞毒性测定

Md. Shahadat Hossain, Sanchita Dewanjee, Md. Ashraful Islam, Mohammad Hamid Al Muktadir, Sushmita Karmokar, Md Kayes Mahmud, Mohammad Hasem Babu, Sujoy Das, Mohammad Shariful Islam, Sonia Ferdousy
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引用次数: 0

摘要

本研究旨在检测紫荆提取物中可能存在的植物化学物质,并对其抗氧化、抗菌和细胞毒活性进行评价。采用不同化学基团的标准试验方法进行植物化学筛选。为了研究其抗氧化活性,采用了DPPH自由基清除试验和总酚含量测定两种互补试验方法。采用圆盘扩散法评价其体外抗菌活性。采用卤虾致死性生物测定法对其细胞毒活性进行了评价。在DPPH自由基清除试验中,石油醚可溶性组分的自由基清除活性最高,IC50值为40.04 μg/ml。同时与参比标准抗坏血酸进行比较。紫金菊也被发现是总酚含量的良好来源。当浓度为400 μg/盘时,提取物具有中等抑菌活性。在细胞毒活性试验中,石油醚可溶性部位的LC50值为0.703 μg/ml,而标准长春新碱部位的LC50值为0.544 μg/ml。因此,建议进一步研究确定植物提取物具有药理活性的活性化合物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Characterization of phytochemicals and determination of antioxidant, antimicrobial and cytotoxic properties of the medicinal plant Ardisia solanacea
The present study was conducted to detect possible phytochemicals and evaluate antioxidant, antimicrobial and cytotoxic activities of the extract of Ardisia solanacea. Phytochemical screening was carried out using the standard test methods of different chemical group. For investigating the antioxidant activity, two complementary test methods namely DPPH free radical scavenging assay and total phenolic content determination were carried out. For the evaluation of in vitro antimicrobial activity, disc diffusion method was used. Evaluation of cytotoxic activity was done using the brine shrimp lethality bioassay. In DPPH free radical scavenging test, the petroleum ether soluble fraction showed the highest free radical scavenging activity with IC50 value 40.04 μg/ml. while compared to that of the reference standards ascorbic acid. Ardisia solanacea was also found as a good source of total phenolic contents. Moreover, the extracts revealed moderate antimicrobial activity at the concentration of 400 μg/disc. In cytotoxic activity test, the petroleum ether soluble fraction showed significant cytotoxic potential (LC50 value of 0.703 μg/ml) among all the fractions comparing with that of standard vincristine (0.544 μg/ml). Therefore, further studies are suggested to determine the active compounds responsible for the pharmacological activities of the plant extracts.
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