The nonanol/surfactant directed self-assembly supramoleculars heat-shrinkable tubing liquid phase microextraction for determination of flavonoids in natural products combined with high performance liquid chromatography
Jie Li , Weizheng Fu , Yuzhen Zhang , Shuang Hu , Xuan Chen
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引用次数: 0
Abstract
In this paper, a supramolecular heat-shrinkable tubing liquid phase microextraction was developed for the enrichment and determination of flavonoids. The nonanol adsorbed by the heat-shrinkable tubing could induce the surfactant in aqueous solution to self-assembly on its surface, and formed nonanol/CTAB supramolecules in a directional arrangement. The supramolecules structure enhanced the enrichment efficiency of five flavonoids. The parameters affecting the extraction efficiency were optimized, such as the type of organic solvent, concentration of surfactant, pH and volume of sample phase, salt concentration of sample solution, stirring speed and extraction time. The methodological investigation was carried out under the optimal experimental conditions. The enrichment factors of the five analytes were between 72.3 and 93.3. The concentrations of the target analytes showed good linearity between 0.2 and 5 µg/mL, 0.01–1 µg/mL, 0.01–5 µg/mL, respectively. The limit of detection was no more than 25 ng/mL. The procedure was successfully applied in extraction of five flavonoids from the natural products according to its average recoveries of 98.3–101.7 %.
期刊介绍:
This journal is an international medium directed towards the needs of academic, clinical, government and industrial analysis by publishing original research reports and critical reviews on pharmaceutical and biomedical analysis. It covers the interdisciplinary aspects of analysis in the pharmaceutical, biomedical and clinical sciences, including developments in analytical methodology, instrumentation, computation and interpretation. Submissions on novel applications focusing on drug purity and stability studies, pharmacokinetics, therapeutic monitoring, metabolic profiling; drug-related aspects of analytical biochemistry and forensic toxicology; quality assurance in the pharmaceutical industry are also welcome.
Studies from areas of well established and poorly selective methods, such as UV-VIS spectrophotometry (including derivative and multi-wavelength measurements), basic electroanalytical (potentiometric, polarographic and voltammetric) methods, fluorimetry, flow-injection analysis, etc. are accepted for publication in exceptional cases only, if a unique and substantial advantage over presently known systems is demonstrated. The same applies to the assay of simple drug formulations by any kind of methods and the determination of drugs in biological samples based merely on spiked samples. Drug purity/stability studies should contain information on the structure elucidation of the impurities/degradants.