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槲皮素印迹色谱吸附剂再探讨:用于自然资源的合成与再结合方案的优化

Quercetin-imprinted chromatographic sorbents revisited: optimization of synthesis and rebinding protocols for application to natural resources.

作者信息

Pardo Antonelle, Mespouille Laetitia, Blankert Bertrand, Trouillas Patrick, Surin Mathieu, Dubois Philippe, Duez Pierre

机构信息

Laboratory of Therapeutic Chemistry and Pharmacognosy, Faculty of Medicine and Pharmacy, University of Mons - UMONS, Place du Parc 20, 7000 Mons, Belgium(1); Laboratory of Polymeric and Composite Materials, Center of Innovation and Research in Materials and Polymers (CIRMAP), University of Mons - UMONS, Place du Parc 20, 7000 Mons, Belgium; Laboratory of Pharmaceutical Analysis, Faculty of Medicine and Pharmacy, University of Mons - UMONS, Place du Parc 20, 7000 Mons, Belgium; Research Institute for Health Sciences and Technology and Research Institute for Biosciences, Belgium.

Laboratory of Polymeric and Composite Materials, Center of Innovation and Research in Materials and Polymers (CIRMAP), University of Mons - UMONS, Place du Parc 20, 7000 Mons, Belgium.

出版信息

J Chromatogr A. 2014 Oct 17;1364:128-39. doi: 10.1016/j.chroma.2014.08.064. Epub 2014 Aug 27.

Abstract

Molecularly imprinted polymers (MIPs) based on quercetin and synthesized by either bulk, precipitation or suspension polymerization were characterized in terms of size and shape by scanning electron microscopy (SEM) and transmission electron microscopy (TEM). After a study of rebinding protocols, the optimal materials were evaluated as sorbents for solid-phase extraction (SPE) and high-performance liquid chromatography (HPLC) to confirm the presence of imprinted cavities and to assess their selectivity. Besides quercetin, other structurally related natural compounds, naringenin, daidzein and curcumin, were employed for selectivity tests of MIPs. Although rebinding protocols previously described for such MIPs are typically based on binding, washing and eluting methanol-based solutions, we show that this highly polar solvent leads to weak specific interactions (imprinting factor<1) and poor sorbent properties, most probably because of hydrogen-bonding interferences between the MIP and MeOH. Similar experiments performed in tetrahydrofuran yield to much more improved properties (imprinting factor>2.4). This calls for reviewing most of previously published data on quercetin-MIPs; in proper binding conditions, published MIPs may prove more performing than initially assessed. As expected, tested MIPs exhibited the highest selective rebinding towards quercetin template (imprinting effect, quercetin, 3.41; naringenin, 1.54; daidzein, 1.38; curcumin, 1.67); the differences in selectivity between quercetin analogues were explained by the ligand geometries and H-bonding patterns obtained from quantum-chemical calculations. The evaluation of MIPs under identical analytical conditions allowed investigating the effect of the production method on chromatographic performances. The MIPs in bead materials (for quercetin, peak width, 0.69; number of theoretical plates, 143; symmetry factor, 2.22) provided a significant improvement in chromatographic efficiency over the bulk materials (for quercetin, peak width, 1.25; number of theoretical plates, 115; symmetry factor, 2.92). Using the quercetin-beaded MIP as SPE sorbent, quercetin was selectively extracted from Allium cepa L. extract. The MIP developed in this work therefore appears highly promising for the enrichment and determination of quercetin in natural products.

摘要

通过扫描电子显微镜(SEM)和透射电子显微镜(TEM)对基于槲皮素、采用本体聚合、沉淀聚合或悬浮聚合法合成的分子印迹聚合物(MIP)的尺寸和形状进行了表征。在研究了再结合方案后,对最佳材料作为固相萃取(SPE)和高效液相色谱(HPLC)的吸附剂进行了评估,以确认印迹空穴的存在并评估其选择性。除了槲皮素外, 还使用了其他结构相关的天然化合物,如柚皮素、大豆苷元和姜黄素,用于MIP的选择性测试。尽管先前针对此类MIP描述的再结合方案通常基于甲醇基溶液的结合、洗涤和洗脱,但我们发现这种高极性溶剂会导致弱的特异性相互作用(印迹因子<1)和较差的吸附剂性能,这很可能是由于MIP与甲醇之间的氢键干扰。在四氢呋喃中进行的类似实验产生了更好的性能(印迹因子>2.4)。这就需要重新审视以前发表的关于槲皮素-MIP的大部分数据;在合适的结合条件下,已发表的MIP可能比最初评估的性能更好。正如预期的那样,测试的MIP对槲皮素模板表现出最高的选择性再结合(印迹效应,槲皮素为3.41;柚皮素为1.54;大豆苷元为1.38;姜黄素为1.67);槲皮素类似物之间选择性的差异由量子化学计算得到的配体几何结构和氢键模式解释。在相同分析条件下对MIP进行评估,可以研究生产方法对色谱性能的影响。珠状材料中的MIP(对于槲皮素,峰宽为0.69;理论塔板数为143;对称因子为2.22)比本体材料(对于槲皮素,峰宽为1.25;理论塔板数为115;对称因子为2.92)的色谱效率有显著提高。使用槲皮素珠状MIP作为SPE吸附剂,从洋葱提取物中选择性提取了槲皮素。因此,本研究中开发的MIP在天然产物中槲皮素富集和测定方面显示出巨大的应用前景。

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