盐辅助液液萃取和柱上浓缩用于色谱测定啤酒中的酚类化合物

IF 5.2 Q1 CHEMISTRY, ANALYTICAL Advances in Sample Preparation Pub Date : 2024-02-01 DOI:10.1016/j.sampre.2024.100107
Luís Claudio Martins , Maria Soledad M.S.F. Acevedo , Mariana R. Gama , Fábio R.P. Rocha
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引用次数: 0

摘要

对盐辅助液液萃取(SALLE)和柱上浓缩进行了评估,以简化啤酒中酚类化合物的色谱测定。白藜芦醇、类黄酮(槲皮素和山柰叶醇)和酚酸(咖啡酸、对香豆素和反式阿魏酸)被用作模型化合物,以它们在手工啤酒中的含量为依据。使用乙腈的 SALLE 可以有效地净化样品,回收率在 84% 至 112% 之间。柱上浓缩是在反相模式下用酸化水(样品载流)开始梯度洗脱,在高效液相色谱中进行的。因此,分析物被保留在窄带内,而高极性/离子潜在干扰物则被冲出色谱柱。在 10 至 200 µL 范围内,峰面积与进样体积之间呈线性相关(r ≥ 0.999),峰宽(< 10%)或保留时间(< 0.7%)无明显变化,且峰对称(尾随因子在 0.8-1.1 范围内),这证明了该方法的有效性。对所有分析物而言,从 100 微克/升到 1000 微克/升(r >0.999)均呈线性响应,检测限在 9-82 微克/升范围内。在连续进样色谱法(SIC)中,该方法对白藜芦醇、槲皮素和山奈酚的柱上浓度也很有效,进样量可达 750 µL,线性响应范围为 100-1000 µg L-1(r > 0.997)。该建议减少了有机溶剂的消耗(在 SIC 中每次测定仅需 770 µL),并避免使用固相萃取柱进行分析物预浓缩。
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Salt-assisted liquid-liquid extraction and on-column concentration for chromatographic determination of phenolic compounds in beer

Salt-assisted liquid-liquid extraction (SALLE) and on-column concentration were evaluated to simplify the chromatographic determination of phenolic compounds in beer. Resveratrol, flavonoids (quercetin and kaempferol), and phenolic acids (caffeic, p-coumaric, and trans-ferulic acids) were used as model compounds based on their concentrations reported in craft beers. SALLE with acetonitrile was effective for sample cleanup, with recoveries ranging from 84% to 112%. The on-column concentration was carried out in high performance liquid chromatography by starting the gradient elution with acidified water (sample carrier stream) in a reversed-phase mode. Consequently, the analytes were retained in a narrow band, and highly polar/ionic potentially interfering species were flushed from the column. The effectiveness of the approach was demonstrated by linear correlations between the peak areas and the injected volumes from 10 to 200 µL (r ≥ 0.999), without significant variations in peak width (< 10%) or retention times (< 0.7%), and peak symmetry (tailing factors within the range of 0.8–1.1). For all analytes, a linear response was achieved from 100 to 1000 µg L−1 (r > 0.999), with limits of detection within the range of 9–82 µg L−1. The approach was also effective for on-column concentrations of resveratrol, quercetin, and kaempferol in sequential injection chromatography (SIC), with injected volumes up to 750 µL and linear responses within 100–1000 µg L−1 (r > 0.997). The proposal reduced consumption of organic solvents (with only 770 µL required per determination in SIC) and avoided solid-phase extraction cartridges for analyte preconcentration.

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