4.4 Article

Ultra-High-Performance Micellar Liquid Chromatography Comparing Tween 20 and Tween 40 for the Determination of Hydroxycinnamic Acids

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卷 9, 期 3, 页码 -

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MDPI
DOI: 10.3390/separations9030061

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micellar liquid chromatography; Tween surfactants; hydroxycinnamic acid derivatives

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A simple and green micellar liquid chromatography method using Tween 20 and Tween 40 as mobile phase modifiers was developed for the separation of hydroxycinnamic acid derivatives. The method showed faster separation and less peak tailing using Tween 20 compared to Tween 40.
A simple and green ultra-high-performance micellar liquid chromatography (MLC) method was developed here, comparing Tween 20 and Tween 40 for the first time as the only mobile phase modifiers with a C18 column. Its application to the separation of nine hydroxycinnamic acid (HCA) derivatives (cinnamic, caffeic, ferulic, sinapic, o-, m-, p-coumaric, 3,4-dihydroxyhydrocinnamic, and chlorogenic acids) was made, due to their importance as antioxidants in a variety of natural beverages such as wine and coffee. The optimal conditions of 45 degrees C temperature (T), 1% surfactant in the mobile phase, and pH control with 2.5 mM sulfuric acid were determined and used to elucidate the analytical figures of merit. Although the effect of these conditions was insignificant between the two surfactants, the nine-component HCA mixture was separated faster-in about 15 min-and with less peak tailing using Tween 20 than with Tween 40. The linearity of the Vant Hoff (ink versus 1/T) plots was evident for Tween 20, indicating a single retention mechanism-but less so for Tween 40. The equilibrium constants of the analytes with the micelles and the stationary phase were calculated. The developed method was successfully used to analyze organic red wine, spiked organic red wine, and green coffee diet pills. The percent recoveries of the nine HCA compounds spiked in the organic red wine ranged from 90% to 107%. The green coffee extract diet pills showed the presence of a significant amount of chlorogenic acid.

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