Please use this identifier to cite or link to this item: http://elar.urfu.ru/handle/10995/111960
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dc.contributor.authorAlenkina, I. V.en
dc.contributor.authorKis, V. K.en
dc.contributor.authorFelner, I.en
dc.contributor.authorKuzmann, E.en
dc.contributor.authorKlencsár, Z.en
dc.contributor.authorOshtrakh, M. I.en
dc.date.accessioned2022-05-12T08:26:20Z-
dc.date.available2022-05-12T08:26:20Z-
dc.date.issued2020-
dc.identifier.citationStructural and Magnetic Study of the Iron Cores in Iron(III)-Polymaltose Pharmaceutical Ferritin Analogue Ferrifol® / I. V. Alenkina, V. K. Kis, I. Felner et al. // Journal of Inorganic Biochemistry. — 2020. — Vol. 213. — 111202.en
dc.identifier.issn0162-0134-
dc.identifier.otherAll Open Access, Green3
dc.identifier.urihttp://elar.urfu.ru/handle/10995/111960-
dc.description.abstractIron(III)-polymaltose pharmaceutical ferritin analogue Ferrifol® was investigated by high resolution transmission electron microscopy (HRTEM), X-ray diffraction, thermogravimetry, electron magnetic resonance (EMR) spectroscopy, direct current magnetization measurements and 57Fe Mössbauer spectroscopy to get novel information about the structural arrangement of the iron core. The Ferrifol® Mössbauer spectra measured in the range from 295 K to 90 K demonstrated non-Lorentzian two-peak pattern. These spectra were better fitted using a superposition of 5 quadrupole doublets with the same line width. The obtained Mössbauer parameters were different and an unusual line broadening with temperature decrease was observed. Measurements of the Ferrifol® Mössbauer spectra from 60 K to 20 K demonstrated a slow decrease of magnetic relaxation in the iron core. Zero-field-cooled and field-cooled magnetization measurements revealed a blocking temperature at ~33 K and a paramagnetic state of the Ferrifol® iron core at higher temperatures. Isothermal magnetization measurements at 5 K show that the saturation magnetic moment is ~0.31 emu/g. X-band EMR spectroscopy measurements revealed the presence of different magnetic species in the sample. Transmission electron microscopy demonstrated that the size of the iron cores in Ferrifol® is in the range 2–6 nm. The lattice periodicity in these iron cores, measured on the HRTEM images, vary in the range 2.2–2.7 Å. This can be best understood as sets of close packed O(OH) layers in ferrihydrite cores without long range correlation. © 2020 Elsevier Inc.en
dc.description.sponsorshipThe authors wish to thank Prof. Ferenc Simon (Institute of Physics, Budapest University of Technology and Economics, Budapest, Hungary) for making available the applied spectrometer for recording the EMR spectra and Dr. A.V. Chukin (Institute of Physics and Technology, Ural Federal University, Ekaterinburg, Russian Federation) for XRD measurements. This work was supported by the Ministry of Science and Higher Education of the Russian Federation, project No FEUZ-2020-0060, and Act 211 of the Government of the Russian Federation, contract No 02.A03.21.0006. V.K.K. was supported by the János Bolyai Postdoctoral Fellowship of the Hungarian Academy of Sciences and the ÚNKP-19-4 New National Excellence Program of the Ministry for Innovation and Technology. HRTEM facility at the Centre for Energy Research was granted by the European Structural and Investment Funds, grant no. VEKOP-2.3.3-15-2016-00002. This work was in part supported by the Hungarian National Research, Development and Innovation Office – NKFIH (K115784, K115913 and K134770). This work was carried out within the Agreement of Cooperation between the Ural Federal University (Ekaterinburg) and the Eötvös Loránd University (Budapest).en
dc.format.mimetypeapplication/pdfen
dc.language.isoenen
dc.publisherElsevier Inc.en1
dc.publisherElsevier BVen
dc.rightsinfo:eu-repo/semantics/openAccessen
dc.sourceJ. Inorg. Biochem.2
dc.sourceJournal of Inorganic Biochemistryen
dc.subjectFERRIFOL® AND FERRITINen
dc.subjectHIGH RESOLUTION TRANSMISSION ELECTRON MICROSCOPYen
dc.subjectIRON COREen
dc.subjectMAGNETIZATION MEASUREMENTSen
dc.subjectMÖSSBAUER SPECTROSCOPYen
dc.subjectFERRIC HYDROXIDEen
dc.subjectFERRIFOLen
dc.subjectFERRITINen
dc.subjectIRON 57en
dc.subjectIRON POLYMALTOSEen
dc.subjectLIQUID NITROGENen
dc.subjectUNCLASSIFIED DRUGen
dc.subjectDRUGen
dc.subjectFERRIC IONen
dc.subjectFERRITINen
dc.subjectMALTOSEen
dc.subjectARTICLEen
dc.subjectCOMPARATIVE STUDYen
dc.subjectCONTROLLED STUDYen
dc.subjectDIRECT CURRENTen
dc.subjectDRUG STRUCTUREen
dc.subjectELECTRON SPIN RESONANCEen
dc.subjectHIGH RESOLUTION TRANSMISSION ELECTRON MICROSCOPYen
dc.subjectISOTHERMen
dc.subjectMAGNETIC FIELDen
dc.subjectMICROWAVE RADIATIONen
dc.subjectMOSSBAUER SPECTROSCOPYen
dc.subjectPERIODICITYen
dc.subjectQUADRUPOLE MASS SPECTROMETRYen
dc.subjectSCANNING TRANSMISSION ELECTRON MICROSCOPYen
dc.subjectTEMPERATURE DEPENDENCEen
dc.subjectTHERMOGRAVIMETRYen
dc.subjectTRANSMISSION ELECTRON MICROSCOPYen
dc.subjectX RAY DIFFRACTIONen
dc.subjectX RAY POWDER DIFFRACTIONen
dc.subjectCHEMICAL STRUCTUREen
dc.subjectCHEMISTRYen
dc.subjectMAGNETISMen
dc.subjectTEMPERATUREen
dc.subjectFERRIC COMPOUNDSen
dc.subjectFERRITINSen
dc.subjectMAGNETICSen
dc.subjectMALTOSEen
dc.subjectMICROSCOPY, ELECTRON, TRANSMISSIONen
dc.subjectMOLECULAR STRUCTUREen
dc.subjectPHARMACEUTICAL PREPARATIONSen
dc.subjectSPECTROSCOPY, MOSSBAUERen
dc.titleStructural and Magnetic Study of the Iron Cores in Iron(III)-Polymaltose Pharmaceutical Ferritin Analogue Ferrifol®en
dc.typeArticleen
dc.typeinfo:eu-repo/semantics/articleen
dc.typeinfo:eu-repo/semantics/publishedVersionen
dc.identifier.doi10.1016/j.jinorgbio.2020.111202-
dc.identifier.scopus85094963988-
local.contributor.employeeAlenkina, I.V., Department of Experimental Physics, Institute of Physics and Technology, Ural Federal University, Ekaterinburg, 620002, Russian Federation; Kis, V.K., Centre for Energy Research, Konkoly-Thege Miklós út. 29-33, Budapest, 1121, Hungary, Institute of Environmental Sciences, University of Pannonia, Egyetem út. 10, Veszprém, H-8200, Hungary; Felner, I., Racah Institute of Physics, The Hebrew University, Jerusalem, 91904, Israel; Kuzmann, E., Laboratory of Nuclear Chemistry, Institute of Chemistry, Eötvös Loránd University, Budapest, Hungary; Klencsár, Z., Centre for Energy Research, Konkoly-Thege Miklós út. 29-33, Budapest, 1121, Hungary; Oshtrakh, M.I., Department of Experimental Physics, Institute of Physics and Technology, Ural Federal University, Ekaterinburg, 620002, Russian Federationen
local.volume213-
dc.identifier.wos000594687700006-
local.contributor.departmentDepartment of Experimental Physics, Institute of Physics and Technology, Ural Federal University, Ekaterinburg, 620002, Russian Federation; Centre for Energy Research, Konkoly-Thege Miklós út. 29-33, Budapest, 1121, Hungary; Institute of Environmental Sciences, University of Pannonia, Egyetem út. 10, Veszprém, H-8200, Hungary; Racah Institute of Physics, The Hebrew University, Jerusalem, 91904, Israel; Laboratory of Nuclear Chemistry, Institute of Chemistry, Eötvös Loránd University, Budapest, Hungaryen
local.identifier.pure20116710-
local.description.order111202-
local.identifier.eid2-s2.0-85094963988-
local.identifier.wosWOS:000594687700006-
local.fund.feuzFEUZ-2020-0060-
local.identifier.pmid33139022-
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