1. Molecularly imprinted polymer beads for clean-up and preconcentration of β-lactamase-resistant penicillins in milk
- Author
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María C. Moreno-Bondi, Javier L. Urraca, Raquel Chamorro-Mendiluce, and Guillermo Orellana
- Subjects
Polymers ,Penicillins ,010402 general chemistry ,01 natural sciences ,Biochemistry ,High-performance liquid chromatography ,Dicloxacillin ,beta-Lactamases ,Analytical Chemistry ,Molecular Imprinting ,chemistry.chemical_compound ,Limit of Detection ,medicine ,Animals ,Methacrylamide ,Solid phase extraction ,Chromatography, High Pressure Liquid ,Oxacillin ,Detection limit ,Chromatography ,Elution ,Solid Phase Extraction ,010401 analytical chemistry ,Molecularly imprinted polymer ,Anti-Bacterial Agents ,0104 chemical sciences ,Milk ,chemistry ,Molecular imprinting ,Cloxacillin ,medicine.drug - Abstract
This work describes the development and application of class-selective molecularly imprinted polymers (MIPs) for the analysis of beta-lactamase-resistant penicillins, namely cloxacillin (CLOXA), oxacillin (OXA), and dicloxacillin (DICLOXA), in milk samples. Our method is based on molecularly imprinted solid-phase extraction (MISPE) coupled to high-performance liquid chromatography (HPLC) with diode-array detection (DAD). 2-Biphenylylpenicillin (2BPEN), a surrogate with a close resemblance to beta-lactamase-resistant penicillins in terms of size, shape, hydrophobicity, and functionality, was synthesized and used as the template for the polymer synthesis. A MIP library was prepared and screened to select the optimum functional monomer, N-(2-aminoethyl)methacrylamide, and cross-linker, trimethylolpropane trimethacrylate, that provided the best recognition for the target antibiotics. For the MISPE application, the MIPs were prepared in the form of microspheres, using porous silica beads (40-75 μm) as sacrificial scaffolds. The developed MISPE method enables efficient extraction from aqueous samples and analysis of the antimicrobials, when followed by a selective washing with 2 mL acetonitrile-water (20:80 v/v) and elution with 1 mL 0.05 mol L(-1) tetrabutylammonium in methanol. The analytical method was validated according to EU guideline 2002/657/EC. The limits of quantification (S/N = 10) were in the 5.3-6.3 μg kg(-1) range, well below the maximum residue limits (MRLs) currently established. Inter-day mean recoveries were in the range 99-102 % with RSDs below 9 %, improving on the performance of previously reported MISPE methods for the analysis of CLOXA, OXA, or DICLOXA in milk samples.
- Published
- 2015
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