Bioassay-guided isolation of the antioxidant constituent from Kaempferia rotunda L.

Dyah Aryantini, Puji Astuti, Nunung Yuniarti, S. Wahyuono
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Abstract

Abstract. Aryantini D, Astuti P, Yuniarti N, Wahyuono S. 2023. Bioassay-guided isolation of the antioxidant constituent from Kaempferia rotunda L. Biodiversitas 24: 3641-3648. Kaempferia rotunda L. contains various phytochemical compounds with various biological activities and has been widely utilized in traditional medicine. This research focused on exploring bioactive compounds in the ethanol extract of Kaempferia rotunda using radical scavenging (1,1-Diphenyl-2-picrylhydrazyl) bioassay-guided isolation. Initially, the powdered material of K. rotunda was macerated with 70% ethanol and filtered, and the filtrate was evaporated in vacuo to make concentrated ethanol extract. The concentrated ethanol extract was then triturated gradually with increasing polarity of solvents (n-hexane, ethyl acetate, ethanol) to give n-hexane (HSF), ethyl acetate (EASF), ethanol (ESF), and residue (ISF) fractions. Each fraction was tested by DPPH bioassay with quercetin as the positive control to determine the active fraction. The active fraction (ESF) was further fractionated by Vacuum Liquid Chromatography (VLC) using a mobile gradient phase starting from ethyl acetate 100%, acetone 100%, and methanol 100% tomake3 sub-fractions (F1, F2, F3),respectively. The DPPH radical scavenging bioassay showed that F1 was the most active, containing bioactive compound detected by TLC visualized by DPPH. Based on spectroscopic and literature data comparison, this compound was isolated, purified, and identified ascrotepoxide. Crotepoxide displayed IC50of 38.91±0.59 (ABTS), 47.45±0.60 (DPPH),and 26.74±1.23 (FRAP) µg/mL.
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生物测定法分离山柰抗氧化成分。
摘要张建军,张建军,张建军,等。圆形山柰抗氧化成分的生物测定分离。生物多样性,24:3641-3648。圆形山柰含有多种具有多种生物活性的植物化学物质,在传统医学中有着广泛的应用。本研究主要采用自由基清除(1,1-二苯基-2-苦味肼基)生物测定引导分离的方法,探索圆形山奈乙醇提取物中的生物活性化合物。先用70%的乙醇浸泡圆圆菌粉料,过滤后真空蒸发滤液,制成浓缩的乙醇提取物。然后随着溶剂(正己烷、乙酸乙酯、乙醇)极性的增加,将浓缩乙醇提取物逐渐发酵,得到正己烷(HSF)、乙酸乙酯(EASF)、乙醇(ESF)和残渣(ISF)馏分。以槲皮素为阳性对照,采用DPPH生物测定法测定其活性部位。活性组分(ESF)通过真空液相色谱(VLC)进一步分离,采用流动梯度相从100%乙酸乙酯、100%丙酮和100%甲醇开始,分别为F1、F2、F3亚馏分。清除DPPH自由基的生物测定结果表明,F1活性最强,DPPH可视化TLC检测到F1中含有生物活性化合物。基于光谱和文献资料的比较,分离、纯化了该化合物,并鉴定出ascroteoxido。Crotepoxide的ic50分别为38.91±0.59 (ABTS)、47.45±0.60 (DPPH)和26.74±1.23 (FRAP)µg/mL。
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