cris.boxmetadata.label.title
Use of two functional monomers for a new approach to the synthesis of a magnetic molecularly imprinted polymer for ciprofloxacin
cris.boxmetadata.label.dateissued
01 browse.startsWith.months.november 2021
cris.boxmetadata.label.accesslevel
open access
cris.boxmetadata.label.resourcetype
journal article
cris.boxmetadata.label.authors
Silva L.M.
Foguel M.V.
TABOADA SOTOMAYOR, MARIA DEL PILAR
National Institute for Alternative Technologies of Detection, Toxicological Evaluation & Removal of Mi-cropollutants and Radioactives (INCT-DATREM)
cris.boxmetadata.label.publisher
Elsevier Editora Ltda
cris.boxmetadata.label.abstract
Ciprofloxacin is an antibiotic widely used in the treatment of human and animal diseases and can be found as a contaminant in some foods of animal origin, such as milk. Thus, the use of molecularly imprinted polymers based on magnetic nanoparticles (mag-MIP) has interesting advantages for extraction in complex samples. Mag-MIP selectivity is provided by careful selection of the functional monomer that will interact with specific groups of the model molecule. Thus, this work presents, for the first time, the performance comparison of mag-MIPs for ciprofloxacin that were synthesized using one functional monomer (mag-MIP1) the acrylic acid, as well as two functional monomers (mag-MIP2), using acrylic acid and 1-vinylimidazole. Both polymers were characterized using different techniques, and the conditions for rebinding the analyte to specific cavities were optimized. Mag-MIP2 showed faster rewiring of ciprofloxacin to polymeric cavities (30 min versus 120 min for mag-MIP1) and better selectivity. Both magnetic polymers were applied to samples of whole and skimmed milk and showed that the percentage range of ciprofloxacin adsorbed to mag-MIP1 was 47–98%, while that for mag-MIP2 was 87–99%. Therefore, mag-MIP synthesized with two functional monomers (mag-MIP2) showed a more promising performance to be applied in the extraction of ciprofloxacin in complex matrices, such as milk.
cris.boxmetadata.label.citationstartpage
511
cris.boxmetadata.label.citationendpage
523
cris.boxmetadata.label.volume
15
cris.boxmetadata.label.language
English
cris.boxmetadata.label.ocdeknowledgeArea
Química
Métodos de investigación bioquímica
cris.boxmetadata.label.subjects
cris.boxmetadata.label.doi
cris.boxmetadata.label.scopusidentifier
2-s2.0-85113559859
cris.boxmetadata.label.source
Journal of Materials Research and Technology
cris.boxmetadata.label.containerissn
22387854
cris.boxmetadata.label.sponsor
The authors are grateful for the financial support for this research project provided by the Brazilian National Council for Scientific and Technological Development (CNPq, grants #408050/2018-7 and #465571/2014-0 ), FAPESP (grants #2019/00677-7 and #2014/25264-3 ). LMS wishes to thank to the Coordination of Superior Level Staff Improvement (CAPES) for provision Master scholarships.
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Directorio de Producción Científica
Scopus