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Antioxidant activities of ethanol extracts from Zanthoxylum avicennae

机译:Zanthoxylum avicennae的乙醇提取物的抗氧化活性

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The Zanthoxylum avicennae 95% EtoH extracts after concentration were dissolved in H_2O and extracted with EtoAc and n-BuOH Successively. The n-BuOH layer was added to Diaion HP-20 macroporous resin column, then the resin was washed by distilled water to get rid of impurity, then washed by 20%, 40% and 60% methanol individually, and obtained M20, M40 and M60 respectively. And antioxidant activity was assessed using three methods: DPPH radical-scavenging activity, ABTS+ radical-scavenging activity, ferric reducing antioxidant power (FRAP) assay. The results indicate that TEAC value of M40 were higher than other part extracted from Zanthoxylum avicennae 95% EtoH extracts during three methods. The results of the experiments also can find M40 is the strongest antioxidant activity part in Zanthoxylum avicennae 95% EtoH extracts and provide reference for further isolating the part M_(40).
机译:浓度浓缩后的Zanthoxylum avicennae 95%EtOH萃取物在H_2O中溶解在H_2O中并连续用EtOAc和N-BuOH萃取。将N-BuOH层加入曲调HP-20大孔树脂柱中,然后通过蒸馏水洗涤树脂以脱离杂质,然后单独洗涤20%,40%和60%甲醇,得到M20,M40和分别为M60。使用三种方法评估抗氧化活性:DPPH自由基清除活性,ABTS +自由基清除活性,公共减少抗氧化能力(FRAP)测定。结果表明,在三种方法中,M40的M40的TeaC值高于来自Zanthoxylum Avicennae 95%EtOH提取物的其他部分。实验的结果也可以发现M40是Zanthoxylum禽类95%EtOH提取物中最强的抗氧化活性部分,并为进一步分离部分M_(40)提供参考。

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