Efficient and Selective Separation of Metronidazole From Human Serum by Using Molecularly Imprinted Magnetic Nanoparticles

dc.contributor.author Bilici, Mustafa
dc.contributor.author Zengin, Adem
dc.contributor.author Ekmen, Elvan
dc.contributor.author Cetin, Demet
dc.contributor.author Aktas, Nahit
dc.date.accessioned 2025-05-10T17:05:11Z
dc.date.available 2025-05-10T17:05:11Z
dc.date.issued 2018
dc.description Cetin, Demet/0000-0003-1186-4229; Zengin, Adem/0000-0002-6889-5387; Aktas, Nahit/0000-0001-9341-607X en_US
dc.description.abstract Magnetic molecularly imprinted nanoparticles were prepared through surface-initiated reversible addition fragmentation chain transfer polymerization by using metronidazole as a template. The molecularly imprinted magnetic nanoparticles were characterized by attenuated total reflection Fourier transform infrared spectroscopy, X-ray photoelectron spectroscopy, transmission electron microscopy, X-ray diffraction, and vibrating sample magnetometry. The adsorption characteristics were also investigated and the kinetics of the adsorption of metronidazole on the imprinted nanoparticles were described by the second-order kinetic model with the short equilibrium adsorption time (30min). The adsorption isotherm was well matched with the Langmuir isotherm in which the maximum adsorption capacity was calculated to be 40.1mg/g. Furthermore, the imprinted magnetic nanoparticles showed good selectivity as well as reusability even after six adsorption-desorption cycles. The imprinted magnetic nanoparticles were used as a sorbent for the selective separation of metronidazole from human serum. The recoveries of metronidazole from human serum changed between 97.5 and 99.8% and showed similar sensitivity as an enzyme-linked immunoassay method. Therefore, the molecularly imprinted magnetic nanoparticles might have potential application for the selective and reliable separation of metronidazole from biological fluids in clinical applications. en_US
dc.description.sponsorship Research Fund of the Van Yuzuncu Yil University [FBA-2017-5804] en_US
dc.description.sponsorship Mustafa Bilici and Adem Zengin are grateful for the financial support from the Research Fund of the Van Yuzuncu Yil University (Project No. FBA-2017-5804). en_US
dc.identifier.doi 10.1002/jssc.201800428
dc.identifier.issn 1615-9306
dc.identifier.issn 1615-9314
dc.identifier.scopus 2-s2.0-85050484249
dc.identifier.uri https://doi.org/10.1002/jssc.201800428
dc.identifier.uri https://hdl.handle.net/20.500.14720/6220
dc.language.iso en en_US
dc.publisher Wiley-v C H verlag Gmbh en_US
dc.rights info:eu-repo/semantics/closedAccess en_US
dc.subject Magnetic Nanoparticles en_US
dc.subject Metronidazole en_US
dc.subject Molecularly Imprinted Polymers en_US
dc.subject Selective Separation en_US
dc.title Efficient and Selective Separation of Metronidazole From Human Serum by Using Molecularly Imprinted Magnetic Nanoparticles en_US
dc.type Article en_US
dspace.entity.type Publication
gdc.author.id Cetin, Demet/0000-0003-1186-4229
gdc.author.id Zengin, Adem/0000-0002-6889-5387
gdc.author.id Aktas, Nahit/0000-0001-9341-607X
gdc.author.scopusid 6603833662
gdc.author.scopusid 36718519300
gdc.author.scopusid 57203099739
gdc.author.scopusid 57661109900
gdc.author.scopusid 35434412700
gdc.author.wosid Cetin, Demet/Aag-5793-2019
gdc.author.wosid Aktas, Nahit/Glr-4607-2022
gdc.coar.access metadata only access
gdc.coar.type text::journal::journal article
gdc.description.department T.C. Van Yüzüncü Yıl Üniversitesi en_US
gdc.description.departmenttemp [Bilici, Mustafa] Van Yuzuncu Yil Univ, Fac Sci & Arts, Dept Chem, Van, Turkey; [Zengin, Adem; Ekmen, Elvan; Aktas, Nahit] Van Yuzuncu Yil Univ, Fac Engn, Dept Chem Engn, TR-65080 Van, Turkey; [Cetin, Demet] Gazi Univ, Gazi Fac Educ, Dept Math & Sci Educ, Ankara, Turkey en_US
gdc.description.issue 14 en_US
gdc.description.publicationcategory Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı en_US
gdc.description.scopusquality Q2
gdc.description.volume 41 en_US
gdc.description.woscitationindex Science Citation Index Expanded
gdc.description.wosquality Q2
gdc.identifier.pmid 29813175
gdc.identifier.wos WOS:000439808600010
gdc.index.type WoS
gdc.index.type Scopus
gdc.index.type PubMed

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