Oxytetracycline recovery from aqueous media using computationally designed molecularly imprinted polymers

Date

2016-08-03

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Publisher

Springer Verlag (Germany)

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Article

ISSN

1618-2642

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Citation

Rodríguez-Dorado R, Carro AM, Chianella I, et al., Oxytetracycline recovery from aqueous media using computationally designed molecularly imprinted polymers, Analytical and Bioanalytical Chemistry, Vol. 408, Issue 24, September 2016, pp. 6845-6856

Abstract

Polymers for recovery/removal of the antimicrobial agent oxytetracycline (OTC) from aqueous media were developed with use of computational design and molecular imprinting. 2-Hydroxyethyl methacrylate, 2-acrylamide-2-methylpropane sulfonic acid (AMPS), and mixtures of the two were chosen according to their predicted affinity for OTC and evaluated as functional monomers in molecularly imprinted polymers and nonimprinted polymers. Two levels of AMPS were tested. After bulk polymerization, the polymers were crushed into particles (200–1000 μm). Pressurized liquid extraction was implemented for template removal with a low amount of methanol (less than 20 mL in each extraction) and a few extractions (12–18 for each polymer) in a short period (20 min per extraction). Particle size distribution, microporous structure, and capacity to rebind OTC from aqueous media were evaluated. Adsorption isotherms obtained from OTC solutions (30–110 mg L-1) revealed that the polymers prepared with AMPS had the highest affinity for OTC. The uptake capacity depended on the ionic strength as follows: purified water > saline solution (0.9 % NaCl) > seawater (3.5 % NaCl). Polymer particles containing AMPS as a functional monomer showed a remarkable ability to clean water contaminated with OTC. The usefulness of the stationary phase developed for molecularly imprinted solid-phase extraction was also demonstrated.

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Software Description

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Github

Keywords

Computational design, Molecularly imprinted polymer, Oxytetracycline, Rebinding isothern, Solid-phase extraction, Groundwater remediation

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Attribution-NonCommercial 4.0 International

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