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Simultaneous determination of theophylline, theobromine and caffeine in different tea beverages by graphene-oxide based ultrasonic-assisted dispersive micro solid-phase extraction combined with HPLC-UV

机译:氧化石墨烯-超声辅助微分散固相萃取-HPLC-UV法同时测定茶饮料中茶碱,可可碱和咖啡因

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摘要

A simple ultrasound-assisted dispersive micro-solid phase extraction method based on graphene-oxide (GO) nanosorbents (UAD-mu-SPE), followed by high performance liquid chromatography-ultraviolet detection (HPLC-UV) was developed for the simultaneous determination of theophylline, theobromine and caffeine in different infusion tea samples. GO was synthesized by Hummers method and characterized with field emission-scanning electron microscopy (FE-SEM), X-ray diffraction (XRD), and Fourier transform infrared (FT-IR) spectroscopy. The GO sorbent was dispersed in the sample solution with the assistance of ultrasound to enhance adsorption and desorption performance and rates. The main parameters influencing the extraction efficiency, including desorption solvent (type and volume), sorbent dosage, adsorption time, desorption time, and ionic strength were studied and optimized by a one factor at a time method. The best performance of the method was achieved with 3 mg mL(-1) of GO, adsorption time of 15 min, desorption time of 4 min, salt concentration of 5%, and 100 mu L of desorption solvent (alkaline methanol). Under the optimized conditions, the limit of detection (LOD) and limit of quantification (LOQ) were attained in the ranges 0.11-0.90 ng mL(-1) and 0.37-3.00 ng mL(-1), respectively. The method showed a good linearity in the range of 0.003-5 mu g mL(-1) with a coefficient of determination (R-2) higher than 0.986. The repeatability and reproducibility of the method were 1.80% and 2.9%, respectively. The developed technique (GO-UAD-mu-SPE) was successfully applied to the determination of the analytes in beverage tea samples including black, white, oolong, and green teas with the relative recoveries in the range of 84.6-113.6%.
机译:建立了一种基于石墨烯-氧化物(GO)纳米吸附剂(UAD-mu-SPE)的简单的超声辅助分散微固相萃取方法,然后采用高效液相色谱-紫外检测(HPLC-UV)进行同时测定不同输液茶样品中的茶碱,可可碱和咖啡因。 GO采用Hummers法合成,并用场发射扫描电子显微镜(FE-SEM),X射线衍射(XRD)和傅立叶变换红外光谱(FT-IR)表征。 GO吸附剂借助超声分散在样品溶液中,以增强吸附和解吸性能以及速率。通过一次因素分析研究和优化了影响萃取效率的主要参数,包括脱附溶剂(类型和体积),吸附剂用量,吸附时间,脱附时间和离子强度。该方法的最佳性能是使用3 mg mL(-1)的GO,15分钟的吸附时间,4分钟的解吸时间,5%的盐浓度和100μL的解吸溶剂(碱性甲醇)获得的。在优化的条件下,检出限(LOD)和定量限(LOQ)分别达到0.11-0.90 ng mL(-1)和0.37-3.00 ng mL(-1)。该方法在0.003-5μg mL(-1)范围内显示出良好的线性,测定系数(R-2)高于0.986。该方法的重复性和重现性分别为1.80%和2.9%。所开发的技术(GO-UAD-mu-SPE)已成功应用于饮料茶样品中的分析物测定,包括黑茶,白茶,乌龙茶和绿茶,相对回收率在84.6-113.6%之间。

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