PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection

Permanent URI for this collectionhttps://hdl.handle.net/11147/7645

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Department: search.filters.department.İzmir Institute of Technology. Materials Science and EngineeringPublisher: search.filters.publisher.Royal Society of Chemistry

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Now showing 1 - 4 of 4
  • Article
    Citation - WoS: 2
    Citation - Scopus: 2
    Size Driven Barrier To Chirality Reversal in Electric Control of Magnetic Vortices in Ferromagnetic Nanodiscs
    (Royal Society of Chemistry, 2022) Aldulaimi, W. A. S.; Okatan, Mahmut Barış; Şendur, Kürşat; Onbaşlı, Mehmet Cengiz; Mısırlıoğlu, İbrahim Burç
    New high density storage media and spintronic devices come about with a progressing demand for the miniaturization of ferromagnetic structures. Vortex ordering of magnetic dipoles in such structures has been repeatedly observed as a stable state, offering the possibility of chirality in these states as a means to store information at high density. Electric pulses and magnetoelectric coupling are attractive options to control the chirality of such states in a deterministic manner. Here, we demonstrate the chirality reversal of vortex states in ferromagnetic nanodiscs via pulsed electric fields using a micromagnetic approach and focus on the analysis of the energetics of the reversal process. A strong thickness dependence of the chirality reversal in the nanodiscs is found that emanates from the anisotropy of the demagnetizing fields. Our results indicate that chiral switching of the magnetic moments in thin discs can give rise to a transient vortex-antivortex lattice not observed in thicker discs. This difference in the chirality reversal mechanism emanates from profoundly different energy barriers to overcome in thin and thicker discs. We also report the polarity-chirality correlation of a vortex that appears to depend on the aspect ratio of the nanodiscs.
  • Article
    Citation - WoS: 67
    Citation - Scopus: 66
    Bilayers of Janus Wsse: Monitoring the Stacking Type: Via the Vibrational Spectrum
    (Royal Society of Chemistry, 2018) Kandemir, Ali; Şahin, Hasan
    Motivated by the recent successful synthesis of Janus type single layers of transition metal dichalcogenides, we investigate the stability, vibrational and electronic properties of the Janus single layer structure of WSSe and its bilayers by means of density functional theory. The structural and vibrational analysis show that the Janus single layer of WSSe forms a dynamically stable structure in the 2H phase. Owing to its non-centrosymmetric structure, the Janus WSSe single layer has two in-plane (E) and two out-of-plane (A) Raman active phonon modes. The eigen-frequencies of the prominent Raman active modes are calculated to be 277 (A) and 322 (E) cm-1. Similar to single layer WS2 and WSe2, Janus WSSe is a direct band gap semiconductor that has two electronically different faces. In addition, the possible bilayer stacking orders of the Janus WSSe single layers are investigated. It is found that there are 3 stacking types of bilayer Janus WSSe and each stacking type has distinctive Raman characteristics in its vibrational spectrum. Our results show that thanks to the vibrational characteristics, which stem from the distinctive interlayer interactions at different sides, the stability and stacking types of the bilayer of WSSe Janus structure can be monitored.
  • Article
    Citation - WoS: 33
    Citation - Scopus: 36
    Epr Studies of Intermolecular Interactions and Competitive Binding of Drugs in a Drug-Bsa Binding Model
    (Royal Society of Chemistry, 2016) Akdoğan, Yaşar; Emrullahoğlu, Mustafa; Tatlıdil, Diğdem; Üçüncü, Muhammed; Çakan Akdoğan, Gülçin
    Understanding intermolecular interactions between drugs and proteins is very important in drug delivery studies. Here, we studied different binding interactions between salicylic acid and bovine serum albumin (BSA) using electron paramagnetic resonance (EPR) spectroscopy. Salicylic acid was labeled with a stable radical (spin label) in order to monitor its mobilized (free) or immobilized (bound to BSA) states. In addition to spin labeled salicylic acid (SL-salicylic acid), its derivatives including SL-benzoic acid, SL-phenol, SL-benzene, SL-cyclohexane and SL-hexane were synthesized to reveal the effects of various drug binding interactions. EPR results of these SL-molecules showed that hydrophobic interaction is the main driving force. Whereas each of the two functional groups (-COOH and -OH) on the benzene ring has a minute but detectable effect on the drug-protein complex formation. In order to investigate the effect of electrostatic interaction on drug binding, cationic BSA (cBSA) was synthesized, altering the negative net charge of BSA to positive. The salicylic acid loading capacity of cBSA is significantly higher compared to that of BSA, indicating the importance of electrostatic interaction in drug binding. Moreover, the competitive binding properties of salicylic acid, ibuprofen and aspirin to BSA were studied. The combined EPR results of SL-salicylic acid/ibuprofen and SL-ibuprofen/salicylic acid showed that ibuprofen is able to replace up to ∼83% of bound SL-salicylic acid, and salicylic acid can replace only ∼14% of the bound SL-ibuprofen. This indicates that ∼97% of all salicylic acid and ibuprofen binding sites are shared. On the other hand, aspirin replaces only ∼23% of bound SL-salicylic acid, and salicylic acid replaces ∼50% of bound SL-aspirin, indicating that ∼73% of all salicylic acid and aspirin binding sites are shared. These results show that EPR spectroscopy in combination with the spin labeling technique is a very powerful method to investigate drug binding dynamics in detail.
  • Article
    Citation - WoS: 24
    Citation - Scopus: 27
    Physiological Concentrations of Albumin Favor Drug Binding
    (Royal Society of Chemistry, 2015) Tatlıdil, Diğdem; Üçüncü, Muhammed; Akdoğan, Yaşar
    The ability to track drug binding and release makes electron paramagnetic resonance (EPR) spectroscopy well suited for drug delivery studies. Using the continuous wave (cw) EPR technique to extract information about the dynamics of the spin labeled drugs we can simultaneously determine the bound and unbound drugs. Here, spin labeled salicylic acid (SLSA) binding to and release from bovine serum albumin (BSA) is investigated, as a model for drug-transport protein interaction. We studied SLSA-BSA binding in a wide concentration range and found that the stoichiometry of the drug-protein increases significantly when the physiological range of BSA concentration is reached. Our EPR results explicitly reveal that up to ∼7 SLSA can bind to one albumin at the physiological concentration, whereas at lower BSA concentrations (<0.125 mM) the SLSA-BSA stoichiometry is maximum 2. Moreover, we studied drug release and showed that the ratio of bound to unbound SLSA concentrations remains relatively stable during dialysis. This indicates that the binding equilibrium of SLSA is not altered through the process of dialysis. This study demonstrates that cw EPR spectroscopy in combination with spin labeled drugs is an effective technique for binding and release studies and stoichiometric analysis of drug-protein interactions.