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基于填充吸附剂数字控制微萃取结合超高压液相色谱的高灵敏度超快分析策略对加香葡萄酒中呋喃衍生物的定量分析

Quantification of furanic derivatives in fortified wines by a highly sensitive and ultrafast analytical strategy based on digitally controlled microextraction by packed sorbent combined with ultrahigh pressure liquid chromatography.

作者信息

Perestrelo Rosa, Silva Catarina L, Câmara José S

机构信息

CQM, Centro de Química da Madeira, Universidade da Madeira, 9000-390, Funchal, Portugal.

CQM, Centro de Química da Madeira, Universidade da Madeira, 9000-390, Funchal, Portugal; Centro de Ciências Exatas e de Engenharia da Universidade da Madeira, Campus Universitário da Penteada, 9000-390 Funchal, Portugal.

出版信息

J Chromatogr A. 2015 Feb 13;1381:54-63. doi: 10.1016/j.chroma.2015.01.020. Epub 2015 Jan 15.

Abstract

An improved, reliable and powerful analytical strategy based on digitally controlled microextraction by packed sorbent (MEPS) combined with ultrahigh pressure liquid chromatography (UHPLC) was validated for the simultaneous identification and quantification of major furanic derivatives, namely 5-hydroxymethyl-2-furaldehyde (5HMF), 5-methyl-2-furaldehyde (5MF), 2-furaldehyde (2F) and 2-furyl methyl ketone (2FMK), in fortified wines. To enhance the extraction efficiency of the target furanic derivates, several influencing extraction parameters, such as number of loading cycles, nature of elution solvent and elution volume, were evaluated and optimized. In addition the ability of different MEPS sorbent materials, namely C2, C8, C18, SIL, M1, R-AX, R-CX and PGC, were also tested. The optimal analytical conditions involved loading 3×200 μL of wine samples through a C8 sorbent in a MEPS syringe placed in the semi-automatic eVolH syringe followed by elution using 200 μL MeOH:H2O (95:5, v/v). The furanic derivates separation was achieved using a CORTECS UPLC(®) C18 analytical column in an ultrafast chromatographic run (within 4 min). The method performance was assessed for dry/medium dry (D/MD) and sweet/medium sweet (S/MS) model wines in terms of selectivity, linearity, limit of detection (LOD), limit of quantitation (LOQ), accuracy, precision and matrix effect, using model wine matrix-matched calibration. Good linearity was obtained with a regression coefficient (r(2)) higher than 0.992. A good precision was attained (RSD<5%) and low LODs were achieved for D/MD (4.5-129.3 ng L(-1)) and S/MS (6.9-285.2 ng L(-1)) model wines. The quantification limits (LOQ) for D/MD model wines ranged from 14.9 to 431.0 ng L(-1), whereas for S/MS model wines range from 23.1 to 950.5 ng L(-1). The method also afforded satisfactory results in terms of accuracy, ranging from 74 to 97% for D/MD wines and between 84 and 99% for S/MS wines. The MEPS(C8)/UHPLC-PDA analytical strategy was successfully applied to analyze furanic derivates in 26 fortified Madeira wines from different types (D/MD, S/MS) and ages. The obtained results revealed the analytical strategy as a suitable tool which combines sensitivity, effectiveness, reduced analysis time and simple analytical procedure. Principal component analysis (PCA) suggested that fortified wines can be organized based on their age on PC1, which are mainly characterized by 5HMF.

摘要

一种基于填充吸附剂数字控制微萃取(MEPS)与超高压液相色谱(UHPLC)联用的改进、可靠且强大的分析策略,用于在强化葡萄酒中同时鉴定和定量主要呋喃衍生物,即5-羟甲基-2-糠醛(5HMF)、5-甲基-2-糠醛(5MF)、2-糠醛(2F)和2-呋喃基甲基酮(2FMK)。为提高目标呋喃衍生物的萃取效率,对多个影响萃取参数,如进样循环次数、洗脱溶剂性质和洗脱体积进行了评估和优化。此外,还测试了不同MEPS吸附剂材料,即C2、C8、C18、SIL、M1、R-AX、R-CX和PGC的性能。最佳分析条件为通过置于半自动eVolH注射器中的MEPS注射器中的C8吸附剂进样3×200μL葡萄酒样品,然后用200μL甲醇:水(95:5,v/v)洗脱。使用CORTECS UPLC® C18分析柱在超快速色谱运行(4分钟内)实现呋喃衍生物的分离。使用模型葡萄酒基质匹配校准,从选择性、线性、检测限(LOD)、定量限(LOQ)、准确度、精密度和基质效应方面评估了该方法对干型/半干型(D/MD)和甜型/半甜型(S/MS)模型葡萄酒的性能。获得了回归系数(r²)高于0.992的良好线性。对于D/MD(4.5 - 129.3 ng L⁻¹)和S/MS(6.9 - 285.2 ng L⁻¹)模型葡萄酒,实现了良好的精密度(RSD<5%)和低检测限。D/MD模型葡萄酒的定量限(LOQ)范围为14.9至431.0 ng L⁻¹,而S/MS模型葡萄酒的定量限范围为23.1至950.5 ng L⁻¹。该方法在准确度方面也获得了令人满意的结果,D/MD葡萄酒的准确度为74%至97%,S/MS葡萄酒的准确度为84%至99%。MEPS(C8)/UHPLC - PDA分析策略成功应用于分析26种来自不同类型(D/MD、S/MS)和年份的马德拉强化葡萄酒中的呋喃衍生物。所得结果表明该分析策略是一种合适的工具,具有灵敏度高、有效性好、分析时间缩短和分析程序简单的特点。主成分分析(PCA)表明,强化葡萄酒可以根据其在PC1上的年份进行分类,主要特征为5HMF。

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