ABSTRACT
Magnetic solid phase extraction (MSPE) have been widely applied in a variety of sample preparation techniques. Herein, Fe3O4@pDA as the sorbents for MSPE, were developed for the determination of phenolic acids and flavonoids in fruit wine samples in combination with LC-MS/MS. The Fe3O4@pDA were characterized by Fourier transform infrared spectroscopy (FT-IR), powder X-ray diffraction (PXRD), transmission electron microscopy (TEM), Superconducting Quantum Interference Device Magnetometer (SQUID) and thermogravimetric analysis (TGA) in detail. In the present study, a new, rapid, and efficient MSPE by LC-MS/MS was established for the extraction and sensitive detection of phenolic acids and flavonoids. Under the optimized condition of extraction procedure including the pH value of 4.0, 10 mg of Fe3O4@pDA, 60 s extraction time, and 600 µL desorption solvent volume, good responses were investigated. Results showed that the limits of detection (S/N = 3) for phenolic acids and flavonoids were in the range of 0.01-0.29 ng/ mL. The correlation coefficients of all analytes were more than 0.9985. The method was satisfactorily used for the detection of eleven analytes, and the recoveries of these targets for the two spiked wines (white grape wine and litchi wine) ranged from 80.03 to 116.68% and from 84.00 to 116.1%, respectively.
Subject(s)
Nanoparticles , Wine , Chromatography, Liquid , Flavonoids , Fruit , Indoles , Magnetic Phenomena , Polymers , Silicon Dioxide/chemistry , Solid Phase Extraction/methods , Spectroscopy, Fourier Transform Infrared , Tandem Mass SpectrometryABSTRACT
Traditional Chinese herbal medicine has long enjoyed the reputation of the world's most advanced system of natural medicine. Pinellia ternata is one of the most commonly used herbs in the traditional Chinese medical science. In this study, five representative ingredients of Pinellia ternata guanosine, methionine, glycine, 3,4-dihydroxybenzaldehyde, and homogentisic acid, were assayed using simple derivatization procedures. Under optimized experimental condition, five analytes in Pinellia ternata were rapidly separated and detected using microchip electrophoresis, affording the benefits of speed, minimal sample requirements, and sensitive on-the-chip electrochemical detection, in 5 min with linearity over a concentration of 20-500 µM (R2 = 0.994) with nearly complete recovery (95.6-98.5%).