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首页> 外文期刊>Journal of chromatography, A: Including electrophoresis and other separation methods >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
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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

机译:基于高灵敏度和超快速分析策略的定量葡萄酒中呋喃衍生物的定量分析,该策略基于填充吸附剂与超高压液相色谱相结合的数控微萃取

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摘要

An improved, reliable and powerful analytical strategy based on digitally controlled microextraction by packed sorbent (MEPS) combined with ultrahigh pressure liquid chromatography ((JHPLC) 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-OC and PGC, were also tested. The optimal analytical conditions involved loading 3 x 200 mu L of wine samples through a C8 sorbent in a MEPS syringe placed in the semi-automatic eVolH syringe followed by elution using 200 mu L MeOH:H2O (95:5, v/v). The furanic derivates separation was achieved using a CORTECS UPLC (R) C18 analytical column in an ultrafast chromatographic run (within 4min). 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.
机译:验证了一种基于填充吸附剂(MEPS)与超高压液相色谱((JHPLC)结合的数控微萃取的改进,可靠且功能强大的分析策略,用于同时鉴定和定量主要呋喃衍生物,即5-羟甲基-2-呋喃醛(5HMF),5-甲基-2-糠醛(5MF),2-糠醛(2F)和2-糠基甲基酮(2FMK),为提高目标呋喃衍生物的提取效率,一些影响提取参数评估和优化了负载循环次数,洗脱溶剂的性质和洗脱体积,此外还对不同的MEPS吸附剂材料C2,C8,C18,SIL,M1,R-AX,R-OC和最佳分析条件包括将3 x 200μL的葡萄酒样品通过C8吸附剂装入置于半自动eVolH注射器中的MEPS注射器中,然后使用200μL MeOH:H2O(95:5 , v / v)。使用CORTECS UPLC C18分析柱在超快色谱运行中(4分钟内)实现呋喃衍生物的分离。对干/中干(D / MD)和甜/中甜(S / MS)模型酒的方法性能进行了评估,包括选择性,线性,检测限(LOD),定量限(LOQ),准确性,精确度和基质效果,使用模型葡萄酒基质匹配校准。获得了良好的线性,回归系数(r(2))高于0.992。 D / MD(4.5-129.3 ng L-1)和S / MS(6.9-285.2 ng L-1)模型酒达到了良好的精度(RSD <5%),并且LOD较低。 D / MD型葡萄酒的定量限(LOQ)为14.9至431.0 ng L-1,而S / MS型葡萄酒的定量限为23.1至950.5 ng L-1。该方法在准确度方面也提供了令人满意的结果,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%。

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