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采用微高效液相色谱法和光电二极管阵列检测法测定水杨苷类化合物。

Determination of salicinoids by micro-high-performance liquid chromatography and photodiode array detection.

作者信息

Rubert-Nason K F, Hedman C J, Holeski L M, Lindroth R L

出版信息

Phytochem Anal. 2014 May-Jun;25(3):185-91. doi: 10.1002/pca.2485.

Abstract

INTRODUCTION

Plant-derived salicinoids (conjugates of glucose and salicylate phenolic moieties) are potent modulators of plant-herbivore interactions. We demonstrate the use of micro-high-performance liquid chromatography (μHPLC) with photodiode-array detection (DAD) for quantification of four salicinoids (salicin, salicortin, hydroxycyclohexen-on-oyl salicortin and tremulacin) in methanolic extracts of Populus.

OBJECTIVE

To develop and implement a solvent-conserving μHPLC method to quantify salicinoids in methanolic extracts of Populus tissue.

METHODS

Salicinoids were extracted from Populus tissue into methanol, filtered, and introduced to μHPLC. Extracted analytes were separated on a Zorbax SB C18-column with a binary gradient of methanol and water (with 2% tetrahydrofuran; 20 μL/min), and quantified by DAD (274 nm). We confirmed measurement reliability through standard addition, comparison with an accepted method, and assessment of chromatographic peak purity by ultraviolet absorbance spectra.

RESULTS

Method detection and quantification limits for the salicinoids as a percentage of dry leaf weight were as follows: salicin (0.1%, 0.2%), salicortin (0.001%, 0.02%), hydroxycyclohexen-on-oyl salicortin (0.02%, 0.06%) and tremulacin (0.0006%, 0.002%). Calibrations by external standardisation were linear over 1.5 orders of magnitude with acceptable accuracy and reproducibility.

CONCLUSION

Micro-HPLC can serve as a solvent-conserving alternative to conventional HPLC for quantification of salicinoids in Populus tissue

摘要

引言

植物来源的水杨苷类化合物(葡萄糖与水杨酸酚类部分的共轭物)是植物与食草动物相互作用的有效调节剂。我们展示了使用带有光电二极管阵列检测(DAD)的微型高效液相色谱(μHPLC)来定量杨树甲醇提取物中的四种水杨苷类化合物(水杨苷、水杨苷配糖体、羟基环己烯酮基水杨苷配糖体和震颤素)。

目的

开发并实施一种节省溶剂的μHPLC方法,以定量杨树组织甲醇提取物中的水杨苷类化合物。

方法

将水杨苷类化合物从杨树组织中提取到甲醇中,过滤后引入μHPLC。提取的分析物在Zorbax SB C18柱上进行分离,采用甲醇和水的二元梯度(含2%四氢呋喃;20 μL/min),并通过DAD(274 nm)进行定量。我们通过标准加入法、与公认方法比较以及通过紫外吸收光谱评估色谱峰纯度来确认测量可靠性。

结果

水杨苷类化合物以干叶重量百分比计的方法检测限和定量限如下:水杨苷(0.1%,0.2%)、水杨苷配糖体(0.001%,0.02%)、羟基环己烯酮基水杨苷配糖体(0.02%,0.06%)和震颤素(0.0006%,0.002%)。外标法校准在1.5个数量级范围内呈线性,具有可接受的准确度和重现性。

结论

微型高效液相色谱可作为传统高效液相色谱的一种节省溶剂的替代方法,用于定量杨树组织中的水杨苷类化合物。

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