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Co-precipitation polymerization of dual functional monomers and polystyrene-co-divinylbenzene for ciprofloxacin imprinted polymer preparation
Novel ciprofloxacin composite imprinted materials are synthesized by using co-precipitation polymerization of dual functional monomers (methacrylic acid and 2-vinylpyridine) and polystyrene-co-divinylbenzene. The intermolecular interactions between monomers and template are evaluated by molecular mo...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9042346/ https://www.ncbi.nlm.nih.gov/pubmed/35497320 http://dx.doi.org/10.1039/d1ra05505d |
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author | Nguyen, Huy Truong Vuong Bui, Nhat Thao Kanhounnon, Wilfried G. Vu Huynh, Kim Long Nguyen, Tran-Van-Anh Nguyen, Hien Minh Do, Minh Huy Badawi, Michael Thach, Ut Dong |
author_facet | Nguyen, Huy Truong Vuong Bui, Nhat Thao Kanhounnon, Wilfried G. Vu Huynh, Kim Long Nguyen, Tran-Van-Anh Nguyen, Hien Minh Do, Minh Huy Badawi, Michael Thach, Ut Dong |
author_sort | Nguyen, Huy Truong |
collection | PubMed |
description | Novel ciprofloxacin composite imprinted materials are synthesized by using co-precipitation polymerization of dual functional monomers (methacrylic acid and 2-vinylpyridine) and polystyrene-co-divinylbenzene. The intermolecular interactions between monomers and template are evaluated by molecular modeling analysis. The physicochemical properties of the obtained polymers are characterized using FT-IR, TGA, and SEM. Batch adsorption experiments are used to investigate adsorption properties (kinetic, pH, and isotherm). These polymers are employed to prepare the solid phase extraction cartridges, and their extraction performances are analyzed by the HPLC-UV method. DFT calculations indicate that hydrogen bonding and π−π stacking are the driving forces for the formation of selective rebinding sites. The obtained polymers exhibit excellent adsorption properties, including fast kinetics and high adsorption capacity (up to 10.28 mg g(−1)) with an imprinted factor of 2.55. The Scatchard analysis indicates the presence of specific high-affinity adsorption sites on the imprinted polymer. These absorbents are employed to extract CIP in river water with recoveries in the range of 65.97–119.26% and the relative standard deviation of 3.59–14.01%. Furthermore, the used cartridges could be reused at least eight times without decreasing their initial adsorption capacity. |
format | Online Article Text |
id | pubmed-9042346 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-90423462022-04-28 Co-precipitation polymerization of dual functional monomers and polystyrene-co-divinylbenzene for ciprofloxacin imprinted polymer preparation Nguyen, Huy Truong Vuong Bui, Nhat Thao Kanhounnon, Wilfried G. Vu Huynh, Kim Long Nguyen, Tran-Van-Anh Nguyen, Hien Minh Do, Minh Huy Badawi, Michael Thach, Ut Dong RSC Adv Chemistry Novel ciprofloxacin composite imprinted materials are synthesized by using co-precipitation polymerization of dual functional monomers (methacrylic acid and 2-vinylpyridine) and polystyrene-co-divinylbenzene. The intermolecular interactions between monomers and template are evaluated by molecular modeling analysis. The physicochemical properties of the obtained polymers are characterized using FT-IR, TGA, and SEM. Batch adsorption experiments are used to investigate adsorption properties (kinetic, pH, and isotherm). These polymers are employed to prepare the solid phase extraction cartridges, and their extraction performances are analyzed by the HPLC-UV method. DFT calculations indicate that hydrogen bonding and π−π stacking are the driving forces for the formation of selective rebinding sites. The obtained polymers exhibit excellent adsorption properties, including fast kinetics and high adsorption capacity (up to 10.28 mg g(−1)) with an imprinted factor of 2.55. The Scatchard analysis indicates the presence of specific high-affinity adsorption sites on the imprinted polymer. These absorbents are employed to extract CIP in river water with recoveries in the range of 65.97–119.26% and the relative standard deviation of 3.59–14.01%. Furthermore, the used cartridges could be reused at least eight times without decreasing their initial adsorption capacity. The Royal Society of Chemistry 2021-10-22 /pmc/articles/PMC9042346/ /pubmed/35497320 http://dx.doi.org/10.1039/d1ra05505d Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/ |
spellingShingle | Chemistry Nguyen, Huy Truong Vuong Bui, Nhat Thao Kanhounnon, Wilfried G. Vu Huynh, Kim Long Nguyen, Tran-Van-Anh Nguyen, Hien Minh Do, Minh Huy Badawi, Michael Thach, Ut Dong Co-precipitation polymerization of dual functional monomers and polystyrene-co-divinylbenzene for ciprofloxacin imprinted polymer preparation |
title | Co-precipitation polymerization of dual functional monomers and polystyrene-co-divinylbenzene for ciprofloxacin imprinted polymer preparation |
title_full | Co-precipitation polymerization of dual functional monomers and polystyrene-co-divinylbenzene for ciprofloxacin imprinted polymer preparation |
title_fullStr | Co-precipitation polymerization of dual functional monomers and polystyrene-co-divinylbenzene for ciprofloxacin imprinted polymer preparation |
title_full_unstemmed | Co-precipitation polymerization of dual functional monomers and polystyrene-co-divinylbenzene for ciprofloxacin imprinted polymer preparation |
title_short | Co-precipitation polymerization of dual functional monomers and polystyrene-co-divinylbenzene for ciprofloxacin imprinted polymer preparation |
title_sort | co-precipitation polymerization of dual functional monomers and polystyrene-co-divinylbenzene for ciprofloxacin imprinted polymer preparation |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9042346/ https://www.ncbi.nlm.nih.gov/pubmed/35497320 http://dx.doi.org/10.1039/d1ra05505d |
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