首页> 外文期刊>Journal of chromatography, A: Including electrophoresis and other separation methods >Using of molecularly imprinted polymers for determination of gallic and protocatechuic acids in red wines by high performance liquid chromatography
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Using of molecularly imprinted polymers for determination of gallic and protocatechuic acids in red wines by high performance liquid chromatography

机译:分子印迹聚合物通过高效液相色谱法测定红酒中的没食子酸和原儿茶酸

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The sorption capacities of gallic- and protocatechuic acid-molecularly imprinted polymers (GA-MIP and PCA-MIP, respectively) and non-imprinted polymer (NIP) have been determined on the piston columns by the frontal analyses (FAs). Mobile phases consisted of MeOH, MeOH/H2O (1:1), 12.5% EtOH or ACN. Solutes concentrations used in FAs were 1 mu g/mL and 50 mu g/mL. All sorption capacities were depended on analyte and solvent used. Results obtained from the FAs have shown that both imprinted polymers almost always were preferentially recognized PCA molecule. Only in MeOH, the GA-MIP had ability to recognize its template molecule positively. Surprisingly, in some cases, also the NIP exhibited higher sorption capacities than the MIPs for their templates, e.g. in ACN for GA or in MeOH for PCA. This behaviour indicates that in some solvents, the low affinity sites of the blank polymer can act as strong interacting sites. In the next, prepared MIPs were successfully used as the SPE-sorbents for the extraction and purification of chosen phenolic acids from red wine samples. The recoveries both of MIPs were the highest for PCA, what was in agreement with the experiments carried out in 12.5% EtOH during FAs. Prepared MIP-beads allowed the purification of chosen red wine samples with satisfactory selectivities and high recoveries. The linearity of the method was in the range from 10 mu g/mL to 70 mu g/mL and 0.1 mu g/mL to 4.5 mu g/mL for GA and PCA, respectively, with the determination coefficients ranging from 0.996-0.999. The LODs (S/N = 3) ranged from 0.1 mu g/mL to 0.4 mu g/mL. The RSDs for the recoveries varied from 4.0% to 8.1%. The PAs-MIPs and corresponding NIP were also characterized by attenuated total reflectance analysis Fourier transform infrared spectroscopy (ATR-FTIR) and scanning electron analysis (SEM). (C) 2014 Elsevier B.V. All rights reserved.
机译:通过正面分析(FAs)确定了没食子酸和原儿茶酸分子印迹聚合物(分别为GA-MIP和PCA-MIP)和非印迹聚合物(NIP)的吸附能力。流动相由MeOH,MeOH / H2O(1:1),12.5%EtOH或ACN组成。 FAs中使用的溶质浓度为1μg/ mL和50μg/ mL。所有吸附能力取决于所用分析物和溶剂。从FA获得的结果表明,两种印迹聚合物几乎总是被优先识别的PCA分子。仅在MeOH中,GA-MIP才能够肯定地识别其模板分子。出人意料的是,在某些情况下,NIP的模板,例如MIP的吸附能力也比MIP高。适用于GA的ACN或适用于PCA的MeOH。此行为表明,在某些溶剂中,空白聚合物的低亲和力位点可以充当强相互作用位点。接下来,将制备好的MIP成功用作SPE吸附剂,以从红酒样品中提取和纯化所选的酚酸。两种MIP的回收率均是PCA的最高值,这与FAs期间在12.5%EtOH中进行的实验一致。制备的MIP珠可以纯化出具有满意的选择性和高回收率的红酒样品。对于GA和PCA,该方法的线性分别在10μg / mL至70μg / mL和0.1μg / mL至4.5μg / mL范围内,测定系数在0.996-0.999之间。 LOD(S / N = 3)介于0.1μg / mL至0.4μg / mL之间。回收率的RSD从4.0%到8.1%不等。 PAs-MIPs和相应的NIP也通过衰减全反射分析傅里叶变换红外光谱(ATR-FTIR)和扫描电子分析(SEM)进行表征。 (C)2014 Elsevier B.V.保留所有权利。

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