Khasanah Uswatun, WidyaWaruyanti Aty, Hafid Achmad Fuad, Tanjung Mulyadi
Post Graduate Program, Faculty of Pharmacy, Universitas Airlangga, Surabaya, Indonesia.
Department of Pharmacy, Faculty of Medicine, Brawijaya University, Malang, Indonesia.
Pharmacognosy Res. 2017 Dec;9(Suppl 1):S57-S60. doi: 10.4103/pr.pr_39_17.
was selected from a screening program devoted to search naturally occurring antimalarial compound from plants in Alas Purwo National Park, Banyuwangi, East Java, Indonesia. The previous studies showed that ethanol extract of leaves contains some polyphenol compounds.
This study was designed to isolate and investigate antiplasmodial activity of polyphenol compounds.
The ethanol extract of leaves was fractioned using liquid-liquid fractionation and column chromatography. Isolated compounds were identified using High-performance liquid chromatography, ultraviolet-visible, nuclear magnetic resonance, and compared with references. The isolates were tested for antiplasmodial activity against chloroquine-sensitive 3D7 strain of . Thin blood smears were used to assess the levels of parasitemia and growth inhibition of the isolates.
Half maximal Inhibitory concentration of Gallic acid (1), methyl gallate (2), and kempferol-3-O-rhamnoside (3) were 0.0722 μM, 0.0128 μM, and 3.4595 μM, respectively.
The results suggest that gallic acid, methyl gallate, and kempferol-3-O-rhamnoside isolated from leaves have antiplasmodial activity and are potential to be developed as antimalarial drugs.
The ethanol extract of leaves was successively fractionated in CHCl, EtOAc, and n-butanol. EtOAc fraction was fractionated using column chromatography and purified using preparative thin-layer chromatography (TLC). Isolates were studied for their antiplasmodial activity on parasites culture of chloroquine-sensitive 3D7 strain of . Parasitemia percentages, growth percentages, and inhibition percentages of each group were calculated. The half maximal inhibitory concentration (IC) values that represent the concentration required to inhibit 50% of growth were calculated from a calibration curve using linear regression. The results suggest that isolates have antiplasmodial activity and are responsible in the antimalarial activity of leaves. S.F: Subfraction, EGCG: Epigallocatechingallate, EGC: Epigallocatechin.
该植物样本是从印度尼西亚东爪哇省班尤旺吉的阿拉斯普尔沃国家公园致力于寻找天然抗疟化合物的筛选项目中选取的。先前的研究表明,该植物叶片的乙醇提取物含有一些多酚化合物。
本研究旨在分离并研究多酚化合物的抗疟活性。
采用液 - 液分级分离和柱色谱法对该植物叶片的乙醇提取物进行分级。使用高效液相色谱、紫外 - 可见光谱、核磁共振对分离得到的化合物进行鉴定,并与参考文献进行比较。对分离物针对氯喹敏感的恶性疟原虫3D7株进行抗疟活性测试。使用薄血涂片评估疟原虫血症水平和分离物的生长抑制情况。
没食子酸(1)、没食子酸甲酯(2)和山奈酚 - 3 - O - 鼠李糖苷(3)的半数最大抑制浓度分别为0.0722 μM、0.0128 μM和3.4595 μM。
结果表明,从该植物叶片中分离得到的没食子酸、没食子酸甲酯和山奈酚 - 3 - O - 鼠李糖苷具有抗疟活性,有潜力开发为抗疟药物。
该植物叶片的乙醇提取物先后用氯仿、乙酸乙酯和正丁醇进行分级。乙酸乙酯级分通过柱色谱法进行分级,并用制备薄层色谱(TLC)进行纯化。研究分离物对氯喹敏感的恶性疟原虫3D7株寄生虫培养物的抗疟活性。计算每组的疟原虫血症百分比、生长百分比和抑制百分比。使用线性回归从校准曲线计算代表抑制50%疟原虫生长所需浓度 的半数最大抑制浓度(IC)值。结果表明,分离物具有抗疟活性,并且是该植物叶片抗疟活性的原因所在。S.F:亚级分,EGCG:表没食子儿茶素没食子酸酯,EGC:表没食子儿茶素 。