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投稿时间:2024-05-29
投稿时间:2024-05-29
中文摘要: 以不同蒸馏时段的香茅草精油为研究对象,通过水蒸气蒸馏法提取,气相色谱-质谱(gas chromatographymass spectrometry,GC-MS)法进行成分分析,采用DPPH 自由基清除法、ABTS+自由基清除法对抗氧化能力进行评价。结果表明,在0~10、10~30、30~60、60~360 min 蒸馏时段精油分别鉴定出32、35、34、34 种成分。各蒸馏阶段的主要成分及相对含量不同,0~10、10~30、30~60 min 是橙花醛(35.33%、31.58%、28.47%)、香叶醛(38.50%、32.99%、37.56%),60~360 min 蒸馏时段是正十六酸(18.24%)、橙花醛(8.49%)、香叶醛(12.05%)。不同蒸馏时段精油清除DPPH 自由基的IC50值分别为16.05、7.89、4.03、1.47 mg/mL,清除ABTS+自由基的IC50值分别为3.58、2.40、1.08、0.55 mg/mL。综上所述,香茅草精油具有较强的抗氧化活性,在60~360 min 蒸馏时段精油对DPPH 自由基和ABTS+自由基的清除能力最强。
Abstract:This paper studied the essential oil collected at different distillation periods from Cymbopogon citratus(DC)Stapf.The essential oil was extracted by steam distillation and analyzed by gas chromatography-mass spectrometry(GC-MS). The antioxidant ability of essential oil were evaluated by DPPH radical scavenging method and ABTS+ radical cation scavenging method. It was found that 32,35,34 and 34 components of essential oil were identified in 0-10,10-30,30-60 min and 60-360 min distillation stages respectively. The main components and their relative content were different in each distillation stage. 0-10,10-30,30-60 min distillation periods were rich in neral(35.33%,31.58%,28.47%)and geranial(38.50%,32.99%,37.56%).The major components in 60~360 min distillation periods were n-hexadecanoic acid(18.24%),neral(8.49%)and geranial(12.05%). The IC50 values of essential oil for scavenging DPPH radical were 16.05,7.89,4.03 mg/mL and 1.47 mg/mL,respectively,during different distillation periods. The IC50 values for ABTS+ radical scavenging were 3.58,2.40,1.08 mg/mL and 0.55 mg/mL,respectively. In conclusion,the essential oil of Cymbopogon citratus(DC)Stapf possessed strong antioxidant activities,and the essential oil collected at 60~360 min showed the strongest scavenging activities on DPPH and ABTS+free radicals.
keywords: Cymbopogon citratus(DC)Stapf essential oil distillation periods analysis antioxidant activity
文章编号:202421002 中图分类号: 文献标志码:
基金项目:国家自然科学基金项目(22268012);广西自然科学基金项目(2021GXNSFAA220067)
作者 | 单位 |
何玲利1,张倩1,凌玉钊2,陈房姣3,侯方域1,李梦丹1,田玉红1* | 1.广西科技大学生物与化学工程学院,广西 柳州 545006;2.广西桂味联食品有限公司,广西 柳州 545001;3.广西科技大学医学部,广西 柳州 545006 |
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