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基于溶剂体积比变化的均相液-液微萃取预浓缩及 GC-MS 测定茶和咖啡中的咖啡因。

Preconcentration and GC-MS determination of caffeine in tea and coffee using homogeneous liquid-liquid microextraction based on solvents volume ratio alteration.

机构信息

Department of Chemistry, Faculty of Sciences, Lorestan University, Khoramabad, Iran.

Department of Chemistry, Faculty of Sciences, Lorestan University, Khoramabad, Iran.

出版信息

J Chromatogr B Analyt Technol Biomed Life Sci. 2018 Aug 15;1092:252-257. doi: 10.1016/j.jchromb.2018.06.020. Epub 2018 Jun 12.

Abstract

A simple, fast and green homogeneous liquid-liquid microextraction (HLLME) method based on solvents volume ratio alteration (SVRA) combined with gas chromatography-mass spectrometry (GC-MS) was developed for the preconcentration and determination of caffeine in tea and coffee samples. In the proposed HLLME-SVRA method, the primary extraction from solid samples was achieved by a 2:1 ethanol-water mixture. A micro-volume of dichloromethane (DCM) formed a homogeneous solvent with this mixture after choosing an appropriate volume ratio between the three solvents. After vigorous shaking, an extra volume of water was added that resulted in phase separation due to the solvents volume ratio alteration. As a result, complete extraction of caffeine was achieved after centrifugation. The sedimented dichloromethane phase was then injected into GC-MS for the analysis. The influence of a number of parameters influencing the efficiency of the extraction was investigated and optimized. Under the optimal conditions, an enrichment factor of 11, a limit of detection of 0.05 μg mL and a limit of quantification of 0.16 μg mL were obtained for caffeine. A linear dynamic range of 0.16 to 50 μg mL and a determination coefficient (R) of 0.9980 were achieved. The precision of the method, expressed as relative standard deviation, was 4.8% for six replicated measurements. The method was successfully applied to the determination of caffeine in tea and coffee samples.

摘要

基于溶剂体积比变化(SVRA)的简单、快速和绿色的均相液-液微萃取(HLLME)方法与气相色谱-质谱联用(GC-MS)相结合,用于茶和咖啡样品中咖啡因的预浓缩和测定。在提出的 HLLME-SVRA 方法中,通过 2:1 的乙醇-水混合物从固体样品中进行初步萃取。选择三种溶剂之间的适当体积比后,微体积的二氯甲烷(DCM)与该混合物形成均相溶剂。剧烈摇晃后,加入更多体积的水,由于溶剂体积比的变化导致相分离。因此,离心后可实现咖啡因的完全萃取。然后将沉淀的二氯甲烷相注入 GC-MS 进行分析。考察并优化了影响萃取效率的许多参数。在最佳条件下,咖啡因的富集因子为 11,检测限为 0.05μg/mL,定量限为 0.16μg/mL。获得了 0.16 至 50μg/mL 的线性动态范围和 0.9980 的测定系数(R)。该方法的精密度,以相对标准偏差表示,对于六个重复测量的结果为 4.8%。该方法成功应用于茶和咖啡样品中咖啡因的测定。

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