山茱萸乙醇叶提取物5的抗疟活性研究

None Einstenia Kemalahayati, None Hilkatul Ilmi, None Agriana Rosmalina Hidayati, None Marsih Wijayanti, None Lidya Tumewu, None Suciati, None Achmad Fuad Hafid, Aty Widyawaruyanti
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The antimalarial activity of all subfractions was assessed using a lactate dehydrogenase (LDH) assay against P. falciparum and the mechanism of action of the PfMQO enzyme. The profiles of the most active subfractions were analyzed using High-Performance Liquid Chromatography (HPLC). Results: The separation of fraction 5 (AAL.E.5) yielded 11 subfractions (AAL.E.5.1–AAL.E.5.11). Screening antimalarial activity at 10 μg/mL in this subfraction showed that only five subfractions (AAL.E.5.6-AAL. E.5.10) inhibited P. falciparum and two subfractions (AAL.E.5.6 and AAL.E.5.10) inhibited the PfMQO enzyme. Only subfraction 6 (AAL.E.5.6) inhibited both, with IC50 values of 6.609 µg/mL and 20.34 µg/mL. The thin layer chromatography profile of AAL.E.5.6 revealed reddish-orange spots, indicating the presence of flavonoid compounds, and was also presumed from the UV-visible to HPLC chromatogram for band I in the 300 – 400 nm range and band II in the 240–285 nm range. 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引用次数: 0

摘要

背景:采用液相色谱法对高原蒿叶提取物(AAL.E)进行分离,得到6个不同馏分。组分5 (AAL.E.5)具有抗疟活性,IC50值为3.71µg/mL。目的:研究AAL.E的抗疟活性。5种抗恶性疟原虫亚组分,抗恶性疟原虫苹果酸醌氧化还原酶(PfMQO)的作用机制及活性物质。方法:aal。e。5采用开柱色谱分离,氯仿-甲醇梯度洗脱,极性依次递增。采用乳酸脱氢酶(LDH)测定对恶性疟原虫的抗疟活性和PfMQO酶的作用机制进行了评估。利用高效液相色谱(HPLC)分析了最有效亚组分的谱图。结果:分离得到11个亚段(aal . e .5.1 ~ aal . e .5.11)。10 μg/mL抗疟活性筛选结果显示,该亚段仅有5个亚段(AAL.E.5.6-AAL.)具有抗疟活性。E.5.10)抑制恶性疟原虫,两个亚组分(AAL.E.5.6和AAL.E.5.10)抑制PfMQO酶。只有亚组分6 (AAL.E.5.6)对两者均有抑制作用,IC50值分别为6.609µg/mL和20.34µg/mL。AAL.E.5.6薄层色谱谱图显示红橙色斑点,提示黄酮类化合物的存在,并且从紫外可见到高效液相色谱在300 ~ 400 nm范围内的I波段和240 ~ 285 nm范围内的II波段推测。结论:亚段6对恶性疟原虫具有抗疟活性,可能与PfMQO的作用机制有关。通过薄层色谱、高效液相色谱和紫外可见光谱分析,认为亚段6为类黄酮。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Antimalarial Potential of Fraction 5 from Ethanolic Leaves Extract of Artocarpus Altilis
Background: Artocarpus altilis leaf extract (AAL.E) was separated by VLC, and six fractions were obtained. Fraction 5 (AAL.E.5) showed antimalarial activity with an IC50 value of 3.71 µg/mL. Objective: This study aimed to determine the antimalarial activity of AAL.E.5 subfractions against P. falciparum, the mechanism of action against Plasmodium Falciparum Malate quinone oxidoreductase (PfMQO), and the active substances. Methods: The AAL.E.5 was separated by open-column chromatography and eluted with chloroform-methanol gradient elution in order of increasing polarity. The antimalarial activity of all subfractions was assessed using a lactate dehydrogenase (LDH) assay against P. falciparum and the mechanism of action of the PfMQO enzyme. The profiles of the most active subfractions were analyzed using High-Performance Liquid Chromatography (HPLC). Results: The separation of fraction 5 (AAL.E.5) yielded 11 subfractions (AAL.E.5.1–AAL.E.5.11). Screening antimalarial activity at 10 μg/mL in this subfraction showed that only five subfractions (AAL.E.5.6-AAL. E.5.10) inhibited P. falciparum and two subfractions (AAL.E.5.6 and AAL.E.5.10) inhibited the PfMQO enzyme. Only subfraction 6 (AAL.E.5.6) inhibited both, with IC50 values of 6.609 µg/mL and 20.34 µg/mL. The thin layer chromatography profile of AAL.E.5.6 revealed reddish-orange spots, indicating the presence of flavonoid compounds, and was also presumed from the UV-visible to HPLC chromatogram for band I in the 300 – 400 nm range and band II in the 240–285 nm range. Conclusion: Subfraction 6 has antimalarial activity against P. falciparum and is thought to have a mechanism of action in PfMQO. Based on the TLC, HPLC, and UV-Vis spectra, subfraction 6 was assumed to be a flavonoid.
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