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

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

Journal of chromatography. A (2014-09-10)
Antonelle Pardo, Laetitia Mespouille, Bertrand Blankert, Patrick Trouillas, Mathieu Surin, Philippe Dubois, Pierre Duez
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.

MATERIALS
Product Number
Brand
Product Description

Supelco
Quercetin, Pharmaceutical Secondary Standard; Certified Reference Material
USP
Quercetin, United States Pharmacopeia (USP) Reference Standard
Sigma-Aldrich
Zirconyl chloride octahydrate, reagent grade, 98%
Sigma-Aldrich
Naringenin, natural (US), 98%
Sigma-Aldrich
Quercetin, ≥95% (HPLC), solid
Supelco
Acrylamide, certified reference material, TraceCERT®, Manufactured by: Sigma-Aldrich Production GmbH, Switzerland
Sigma-Aldrich
Ethylene glycol dimethacrylate, 98%, contains 90-110 ppm monomethyl ether hydroquinone as inhibitor
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Methacrylic anhydride, contains 2,000 ppm topanol A as inhibitor, ≥94%
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Acrylamide, purum, ≥98.0% (GC)
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Triethylamine, for amino acid analysis, ≥99.5% (GC)
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Acrylamide, for Northern and Southern blotting, powder blend
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Triethylamine, BioUltra, ≥99.5% (GC)
Supelco
Acrylamide, analytical standard
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Triethylamine, ≥99.5%
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Triethylamine, puriss. p.a., ≥99.5% (GC)
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Acrylamide, for molecular biology, ≥99% (HPLC)
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Triethylamine, ≥99%
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Acrylamide, suitable for electrophoresis, ≥99%
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(±)-Naringenin, ≥95%
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Acrylamide, suitable for electrophoresis, ≥99% (HPLC), powder
Supelco
Triethylamine, analytical standard
Supelco
(±)-Naringenin, analytical standard
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Triethylamine, for protein sequence analysis, ampule, ≥99.5% (GC)
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Triethylamine, ≥99.5%
Supelco
Curcumin, analytical standard
Supelco
Daidzein, analytical standard
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Perfluoro-1,3-dimethylcyclohexane, technical grade, 80%
Supelco
Acrylamide solution, 40% in H2O, for molecular biology
Sigma-Aldrich
Curcumin, ≥94% (curcuminoid content), ≥80% (Curcumin)
Sigma-Aldrich
Acrylamide solution, 40%, suitable for electrophoresis, sterile-filtered