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首页> 外文期刊>Bulletin of the Korean Chemical Society >Effective Sample Preparation of Polyphenols in Wine Using Deep Eutectic Solvent‐based Dispersive Liquid–Liquid Microextraction HPLC‐UV Determination
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Effective Sample Preparation of Polyphenols in Wine Using Deep Eutectic Solvent‐based Dispersive Liquid–Liquid Microextraction HPLC‐UV Determination

机译:使用深凝胶基溶剂基分散液 - 液体微萃取HPLC-UV测定有效样品制备多酚在葡萄酒中的制备

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Polyphenols are phytochemicals that exist in grapes and are beneficial to human health. In this study, resveratrol, oxyresveratrol, and piceatannol in wine were extracted by deep eutectic solvent dispersive liquid–liquid microextraction (DES‐DLLME), and a method was established for quantifying these polyphenols by high‐performance liquid chromatography‐UV/Vis (HPLC‐UV/Vis). Several parameters pertaining to sample extraction, clean‐up, and concentration were optimized and verified with central composite design (CCD) using Design Expert 11. The optimized sample preparation parameters are as follows: the DES extraction solvent, tributylmethylammonium chloride/decanoic acid (1:3 M ratio); basic solvent, 1.3 mL of 5% potassium bicarbonate; volume of acetic anhydride, 250?μL; derivatization time, 5 min; dispersive solvent, methanol; ratio of extraction and dispersive solvents, 1:5.5; and salt, 1.0 g. Chromatographic separation by HPLC/UV–Vis was performed on an ACME C18 (4.6?mm id ×?150?mm length, 5 μm particle size) column in gradient elution mode using water and 70% methanol. Under the established extraction and HPLC‐UV conditions, the limit of detection (LOD) and limit of quantitation (LOQ) of the three analytes in spiked samples ranged from 1.69 to 2.53?μg/L and 5.64 to 8.42?μg/L, respectively. Recovery studies were performed in low, medium, and high concentration ranges to establish a calibration curve, and the accuracy and precision in the working range were 95.1–108.0% and 1.3–6.7 RSD%, respectively. The calibration curves for quantitative analysis were obtained in the concentration ranges 5.6–56.4, 8.3–82.6, and 8.4–84.2 μg/L, with correlation coefficients (r2) ranging from 0.9947 to 0.9967. The proposed method was applied to the determination of polyphenols in wine samples.
机译:多酚是植物中存在的植物化学品,对人体健康有益。在本研究中,通过深红色溶剂分散液 - 微萃取(DES-DILLME)提取白藜芦醇,oxysveraTrol和Piceatannol,并建立一种方法,用于通过高效液相色谱 - UV / Vis定量这些多酚(HPLC -uv / vis)。利用设计专家11,优化了与样品提取,清理和浓缩有关的几个参数,并用中央复合设计(CCD)进行了验证。优化的样品制备参数如下:DES提取溶剂,丁基甲基氯化铵/癸酸(1 :3米比例);碱性溶剂,1.3ml 5%碳酸氢钾;乙酸酐的体积,250Ωμl;衍生时间,5分钟;分散溶剂,甲醇;提取和分散溶剂的比例,1:5.5;和盐,1.0克。使用水和70%甲醇在梯度洗脱模式下在ACME C18(4.6μmID×150×mm长度,5μm粒度)柱上进行HPLC / UV-Vis的色谱分离。在已建立的提取和HPLC-UV条件下,尖刺样品中三种分析物的检测极限(LOD)和定量限(LOQ)分别为1.69至2.53ΩΩΩ0μg/ l和5.64至8.42ΩΩΩ/ l 。恢复研究在低,培养基和高浓度范围内进行,以建立校准曲线,工作范围内的准确性和精度分别为95.1-108.0%和1.3-6.7卢比%。在浓度范围内得到定量分析的校准曲线,浓度范围为5.6-56.4,8.3-82.6和8.4-84.2μg/ L,其相关系数(R2)范围为0.9947至0.9967。所提出的方法应用于葡萄酒样品中的多酚的测定。

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