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A sensitive microextraction by packed sorbent-based methodology combined with ultra-high pressure liquid chromatography as a powerful technique for analysis of biologically active flavonols in wines

机译:基于填充吸附剂的方法与超高压液相色谱法相结合进行灵敏的微萃取,是分析葡萄酒中生物活性黄酮醇的强大技术

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摘要

A new approach based on microextraction by packed sorbent (MEPS) and reversed-phase high-throughput ultra high pressure liquid chromatography (UHPLC) method that uses a gradient elution and diode array detection to quantitate three biologically active flavonols in wines, myricetin, quercetin, and kaempferol, is described. In addition to performing routine experiments to establish the validity of the assay to internationally accepted criteria (selectivity, linearity, sensitivity, precision, accuracy), experiments are included to assess the effect of the important experimental parameters such as the type of sorbent material (C2, C8, C18, SIL, and C8/SCX), number of extraction cycles (extract-discard), elution volume, sample volume, and ethanol content, on the MEPS performance. The optimal conditions of MEPS extraction were obtained using C8 sorbent and small sample volumes (250 μL) in five extraction cycle and in a short time period (about 5 min for the entire sample preparation step). Under optimized conditions, excellent linearity View the MathML source(Rvalues2>0.9963), limits of detection of 0.006 μg mL−1 (quercetin) to 0.013 μg mL−1 (myricetin) and precision within 0.5–3.1% were observed for the target flavonols. The average recoveries of myricetin, quercetin and kaempferol for real samples were 83.0–97.7% with relative standard deviation (RSD, %) lower than 1.6%. The results obtained showed that the most abundant flavonol in the analyzed samples was myricetin (5.8 ± 3.7 μg mL−1). Quercetin (0.97 ± 0.41 μg mL−1) and kaempferol (0.66 ± 0.24 μg mL−1) were found in a lower concentration.The optimized MEPSC8 method was compared with a reverse-phase solid-phase extraction (SPE) procedure using as sorbent a macroporous copolymer made from a balanced ratio of two monomers, the lipophilic divinylbenzene and the hydrophilic N-vinylpyrrolidone (Oasis HLB) were used as reference. MEPSC8 approach offers an attractive alternative for analysis of flavonols in wines, providing a number of advantages including highest extraction efficiency (from 85.9 ± 0.9% to 92.1 ± 0.5%) in the shortest extraction time with low solvent consumption, fast sample throughput, more environmentally friendly and easy to perform.
机译:一种基于填充吸附剂(MEPS)微萃取和反相高通量超高压液相色谱(UHPLC)方法的新方法,该方法使用梯度洗脱和二极管阵列检测来定量测定葡萄酒中的三种生物活性黄酮醇,杨梅素,槲皮素,和山ka酚,描述。除了进行常规实验以建立符合国际公认标准(选择性,线性,灵敏性,精密度,准确性)的测定方法的有效性外,还包括进行实验以评估重要实验参数(如吸附剂材料的类型(C2) ,C8,C18,SIL和C8 / SCX),萃取循环数(废液丢弃),洗脱量,样品量和乙醇含量对MEPS性能的影响。使用C8吸附剂和少量样品(250μL)在五个萃取周期内和较短的时间段内(整个样品制备步骤约为5分钟)获得了MEPS萃取的最佳条件。在优化条件下,出色的线性度(Rvalues2> 0.9963),目标黄酮醇的检测限为0.006μgmL-1(槲皮素)至0.013μgmL-1(杨梅素),精密度在0.5-3.1%之内。实际样品中杨梅素,槲皮素和山奈酚的平均回收率为83.0–97.7%,相对标准偏差(RSD,%)低于1.6%。获得的结果表明,分析样品中最丰富的黄酮醇为杨梅素(5.8±3.7μgmL-1)。发现槲皮素(0.97±0.41μgmL-1)和山1酚(0.66±0.24μgmL-1)的浓度较低。将优化的MEPSC8方法与以反相固相萃取(SPE)为吸附剂的方法进行了比较由亲脂性二乙烯基苯和亲水性N-乙烯基吡咯烷酮(Oasis HLB)两种单体的平衡比例制成的大孔共聚物用作参考。 MEPSC8方法为分析葡萄酒中的黄酮醇提供了一种有吸引力的替代方法,具有许多优势,包括在最短的萃取时间内具有最高的萃取效率(从85.9±0.9%到92.1±0.5%),低溶剂消耗,快速的样品通量,更环保友好且易于执行。

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