Temperature-assisted ionic liquid dispersive liquid-liquid microextraction combined with high performance liquid chromatography for the determination of anthraquinones in Radix et Rhizoma Rhei samples

被引:75
作者
Zhang, Hong-Fei [1 ,2 ,3 ]
Shi, Yan-Ping [1 ,2 ]
机构
[1] Chinese Acad Sci, Key Lab Chem NW Plant Resources, Lanzhou 730000, Peoples R China
[2] Chinese Acad Sci, Lanzhou Inst Chem Phys, Key Lab Nat Med Gansu Prov, Lanzhou 730000, Peoples R China
[3] Chinese Acad Sci, Grad Univ, Beijing 100039, Peoples R China
基金
中国国家自然科学基金;
关键词
Temperature-assisted ionic liquid dispersive liquid-liquid microextraction; High performance liquid chromatography; Anthraquinones; Radix et Rhizoma Rhei samples; DIODE ARRAY DETECTION; SENSITIVE DETERMINATION; WATER SAMPLES; FLUORESCENCE DETECTION; BIOLOGICAL SAMPLES; MASS-SPECTROMETRY; ORGANIC-COMPOUNDS; MEDICINAL-PLANTS; RHUBARB; DERIVATIVES;
D O I
10.1016/j.talanta.2010.06.008
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
In this article, a novel method termed as temperature-assisted ionic liquid dispersive liquid-liquid microextraction (TA IL-DLLME) combining high performance liquid chromatography with diode array detection (HPLC-DAD) was developed for the determination of anthraquinones in Radix et Rhizoma Rhei samples. The ionic liquid (1-hexyl-3-methylimidazolium hexafluorophosphate) was used to replace volatile organic solvent as an extraction solvent for the extraction of anthraquinones (aloe-emodin, rhein, emodin, chrysophanol and physcion) from Radix et Rhizoma Rhei. Several important parameters influencing the extraction efficiency of TA IL-DLLME such as the type and volume of extraction solvent and disperser solvent, sample pH, extraction time, extraction temperature, centrifugation time as well as salting-out effects were optimized. Under the optimal conditions, the spiked recovery for each analyte was in the range of 95.2-108.5%. The precisions of the proposed method were varied from 1.1% to 4.4% (RSD). All the analytes exhibited good linearity with correlation coefficients (r(2)) ranging from 0.9986 to 0.9996. The limits of detection for all target analytes were ranged from 0.50 to 2.02 mu g L-1 (S/N =3). The experimental results indicated that the proposed method was successfully applied to the analysis of anthraquinones in Radix et Rhizoma Rhei. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:1010 / 1016
页数:7
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