Jinghui Li, Yan Kang, Ying Wang, Jiaxin Liu, Yingting Wang, Sitong Liu, Yunxi Bu, Xiangqun Li, Jiahan Xie, Zhibing Wang
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引用次数: 0
摘要
建立了超声辅助深度共晶溶剂萃取-高效液相色谱-二极管阵列检测器检测丹参中4种脂溶性蒽醌类化合物的方法。根。本研究以正己醇和四丁基氯化铵为原料制备了一系列极性可调的DESs,并对其结构、密度、粘度、pH和热稳定性进行了测定。通过单因素试验和响应面法优化提取条件。研究了超声辅助提取蒽醌类化合物的动力学和热力学性质。结果表明,蒽醌类的标准曲线在0.018 ~ 150µg mL−1范围内呈良好的线性关系(r >;0.9998)。检测限和定量限分别为5.04 ~ 5.60 ng mL−1和16.81 ~ 18.67 ng mL−1。加样回收率为84.1% ~ 95.1%,相对标准偏差不超过4.6%。
Ionic Liquid-Based Polarity-Adjustable Deep Eutectic Solvent Extraction Followed by High-Performance Liquid Chromatography-Diode-Array Detection for the Determination of Liposoluble Anthraquinones in Salvia miltiorrhiza Bge. Root
A simple, green, and efficient ultrasound-assisted deep eutectic solvents (DESs) extraction followed by high-performance liquid chromatography-diode array detector was established to detect four liposoluble anthraquinones in Salvia miltiorrhiza Bge. root. In this study, a series of polarity-adjustable DESs were prepared using n-hexanol and tetrabutylammonium chloride, and their structure, density, viscosity, pH, and thermal stability were determined. The conditions for extraction were optimized through single-factor experiments and response surface methodology. The kinetic and thermodynamic properties associated with the ultrasound-assisted extraction of anthraquinones were investigated. The results showed that the standard curves for anthraquinones showed excellent linearity from 0.018 to 150 µg mL−1 (r > 0.9998). The detection and quantification limits varied from 5.04 to 5.60 ng mL−1 and 16.81 to 18.67 ng mL−1, respectively. The recoveries were measured as 84.1%–95.1%, and the relative standard deviations were not exceeded 4.6%.
期刊介绍:
The Journal of Separation Science (JSS) is the most comprehensive source in separation science, since it covers all areas of chromatographic and electrophoretic separation methods in theory and practice, both in the analytical and in the preparative mode, solid phase extraction, sample preparation, and related techniques. Manuscripts on methodological or instrumental developments, including detection aspects, in particular mass spectrometry, as well as on innovative applications will also be published. Manuscripts on hyphenation, automation, and miniaturization are particularly welcome. Pre- and post-separation facets of a total analysis may be covered as well as the underlying logic of the development or application of a method.