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鱼腥草挥发物的气相色谱-质谱联用分析

GC-MS analyses of the volatiles of Houttuynia cordata Thunb.

作者信息

Yang Zhan-Nan, Luo Shi-Qiong, Ma Jing, Wu Dan, Hong Liang, Yu Zheng-Wen

机构信息

Key Laboratory for Information System of Mountainous Area and Protection of Ecological Environment of Guizhou Province, Guizhou Normal University, Guiyang, PR China.

School of Life Science, Guizhou Normal University, Guiyang, PR China.

出版信息

Pak J Pharm Sci. 2016 Sep;29(5):1591-1600.

Abstract

GC-MS is the basis of analysis of plant volatiles. Several protocols employed for the assay have resulted in inconsistent results in the literature. We developed a GC-MS method, which were applied to analyze 25 volatiles (α-pinene, camphene, β-pinene, 2-methyl-2-pentenal, myrcene, (+)-limonene, eucalyptol, trans-2-hexenal, γ-terpinene, cis-3-hexeneyl-acetate, 1-hexanol, α-pinene oxide, cis-3-hexen-1-ol, trans-2-hexen-1-ol, decanal, linalool, acetyl-borneol, β-caryophyllene, 2-undecanone, 4-terpineol, borneol, decanol, eugenol, isophytol and phytol) of Houttuynia cordata Thunb. Linear behaviors for all analytes were observed with a linear regression relationship (r2>0.9991) at the concentrations tested. Recoveries of the 25 analytes were 98.56-103.77% with RSDs <3.0%. Solution extraction (SE), which involved addition of an internal standard, could avoid errors for factors in sample preparation by steam distillation (SD) and solidphase micro extraction (SPME). Less sample material (≍0.05g fresh leaves of H. cordata) could be used to determine the contents of 25 analytes by our proposed method and, after collection, did not affect the normal physiological activity or growth of H. cordata. This method can be used to monitor the metabolic accumulation of H. cordata volatiles.

摘要

气相色谱 - 质谱联用(GC - MS)是分析植物挥发物的基础。文献中用于该测定的几种方案结果并不一致。我们开发了一种GC - MS方法,用于分析鱼腥草的25种挥发物(α - 蒎烯、莰烯、β - 蒎烯、2 - 甲基 - 2 - 戊烯醛、月桂烯、(+) - 柠檬烯、桉叶油素、反式 - 2 - 己烯醛、γ - 松油烯、顺式 - 3 - 己烯基乙酸酯、1 - 己醇、α - 蒎烯氧化物、顺式 - 3 - 己烯 - 1 - 醇、反式 - 2 - 己烯 - 1 - 醇、癸醛、芳樟醇、乙酰龙脑、β - 石竹烯、2 - 十一酮、4 - 松油醇、龙脑、癸醇、丁香酚、异植物醇和植物醇)。在所测试的浓度下,所有分析物均呈现线性行为,线性回归关系良好(r2>0.9991)。25种分析物的回收率为98.56 - 103.77%,相对标准偏差(RSDs)<3.0%。溶液萃取(SE),包括添加内标物,可以避免因水蒸气蒸馏(SD)和固相微萃取(SPME)样品制备过程中的因素导致的误差。使用我们提出的方法,只需较少的样品量(约0.05g鱼腥草鲜叶)即可测定25种分析物的含量,且采集后不会影响鱼腥草的正常生理活性或生长。该方法可用于监测鱼腥草挥发物的代谢积累。

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