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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
来源:
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.
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页码:1010 / 1016
页数:7
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