4.7 Article

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

Journal

TALANTA
Volume 82, Issue 3, Pages 1010-1016

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.talanta.2010.06.008

Keywords

Temperature-assisted ionic liquid dispersive liquid-liquid microextraction; High performance liquid chromatography; Anthraquinones; Radix et Rhizoma Rhei samples

Funding

  1. Foundation for the National Key Technology Research and Development Program of China [2007BAI37B05]
  2. National Natural Science Foundation of China [20875095]

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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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