| 1. |
- Ansari, Shaquib Rahman, 1993-, et al.
(författare)
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Hyperthermia-Induced In Situ Drug Amorphization by Superparamagnetic Nanoparticles in Oral Dosage Forms
- 2022
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Ingår i: ACS Applied Materials and Interfaces. - : American Chemical Society (ACS). - 1944-8244 .- 1944-8252. ; 14:19, s. 21978-21988
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Tidskriftsartikel (refereegranskat)abstract
- Superparamagnetic iron oxide nanoparticles (SPIONs) generate heat upon exposure to an alternating magnetic field (AMF), which has been studied for hyperthermia treatment and triggered drug release. This study introduces a novel application of magnetic hyperthermia to induce amorphization of a poorly aqueous soluble drug, celecoxib, in situ in tablets for oral administration. Poor aqueous solubility of many drug candidates is a major hurdle in oral drug development. A novel approach to overcome this challenge is in situ amorphization of crystalline drugs. This method facilitates amorphization by molecular dispersion of the drug in a polymeric network inside a tablet, circumventing the physical instability encountered during the manufacturing and storage of conventional amorphous solid dispersions. However, the current shortcomings of this approach include low drug loading, toxicity of excipients, and drug degradation. Here, doped SPIONs produced by flame spray pyrolysis are compacted with polyvinylpyrrolidone and celecoxib and exposed to an AMF in solid state. A design of experiments approach was used to investigate the effects of SPION composition (Zn0.5Fe2.5O4 and Mn0.5Fe2.5O4), doped SPION content (10–20 wt %), drug load (30–50 wt %), and duration of AMF (3–15 min) on the degree of drug amorphization. The degree of amorphization is strongly linked to the maximum tablet temperature achieved during the AMF exposure (r = 0.96), which depends on the SPION composition and content in the tablets. Complete amorphization is achieved with 20 wt % Mn0.5Fe2.5O4 and 30 wt % celecoxib in the tablets that reached the maximum temperature of 165.2 °C after 15 min of AMF exposure. Furthermore, manganese ferrite exhibits no toxicity in human intestinal Caco-2 cell lines. The resulting maximum solubility of in situ amorphized celecoxib is 5 times higher than that of crystalline celecoxib in biorelevant intestinal fluid. This demonstrates the promising capability of SPIONs as enabling excipients to magnetically induce amorphization in situ in oral dosage forms.
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| 2. |
- Breijaert, T. C., et al.
(författare)
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Self-assembly of ferria – nanocellulose composite fibres
- 2022
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Ingår i: Carbohydrate Polymers. - : Elsevier Ltd. - 0144-8617 .- 1879-1344. ; 291
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Tidskriftsartikel (refereegranskat)abstract
- An environmentally benign synthesis of a magnetically responsive carboxymethylated cellulose nanofibril-based material is reported. Applied experimental conditions lead to the in-situ formation of magnetite nanoparticles with primary particle sizes of 2.0–4.0 nm or secondary particles of 3.6–16.4 nm depending on whether nucleation occurred between individual carboxymethylated cellulose nanofibrils, or on exposed fibril surfaces. The increase in magnetite particle size on the cellulose fibril surfaces was attributed to Ostwald ripening, while the small particles formed within the carboxymethyl cellulose aggregates were presumably due to steric interactions. The magnetite nanoparticles were capable of coordinating to carboxymethylated cellulose nanofibrils to form large “fibre-like” assemblies. The confinement of small particles within aggregates of reductive cellulose molecules was most likely responsible for excellent conservation of magnetic characteristics on storage of this material. The possibility for using the material in drug delivery applications with release rate controlled by daylight illumination is presented. © 2022 The Author(s)
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| 3. |
- Clulow, Rebecca, et al.
(författare)
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Magnetic and Structural Properties of the Fe5Si1-xGexB2 System
- 2022
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Ingår i: Journal of Solid State Chemistry. - : Elsevier BV. - 0022-4596 .- 1095-726X. ; 316
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Tidskriftsartikel (refereegranskat)abstract
- A series of compounds with compositions Fe5Si1-xGexB2 were synthesised and their structural and magnetic properties were investigated. The Mo5SiB2-type structure with tetragonal I4/mcm space group is maintained for all compounds with x < 0.15, which is estimated as the compositional limit of the system. The unit cell pa-rameters expand with Ge content before reaching a plateau of a = 5.5581(1) and c = 10.3545(1) angstrom at x = 0.15. The saturation magnetisation (MS) decreased slightly with increasing Ge content whilst the magnetocrystalline anisotropy energy (MAE) remains almost unaffected. The Curie temperature for all compounds studied is at 790 K whilst the spin-reorientation temperature shows suppression from 172 K to 101 K where x = 0.15. Ab Initio calculations reveal an increase in MAE for compositions up to x = 0.25 and a decreased magnitude of MAE of-0.14 MJ/m3 for the hypothetical compound Fe5GeB2 relative to the parent compound Fe5SiB2.
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| 4. |
- Dutta, Soma, et al.
(författare)
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Manipulating ultrafast magnetization dynamics of ferromagnets using the odd-even layer dependence of two-dimensional transition metal di-chalcogenides
- 2024
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Ingår i: Nanoscale. - : Royal Society of Chemistry. - 2040-3364 .- 2040-3372. ; 16:8, s. 4105-4113
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Tidskriftsartikel (refereegranskat)abstract
- Two-dimensional transition metal dichalcogenides (TMDs) have drawn immense interest due to their strong spin-orbit coupling and unique layer number dependence in response to spin-valley coupling. This leads to the possibility of controlling the spin degree of freedom of the ferromagnet (FM) in thin film heterostructures and may prove to be of interest for next-generation spin-based devices. Here, we experimentally demonstrate the odd-even layer dependence of WS2 nanolayers by measurements of the ultrafast magnetization dynamics in WS2/Co3FeB thin film heterostructures by using time-resolved Kerr magnetometry. The fluence (photon energy per unit area) dependent magnetic damping (alpha) reveals the existence of broken symmetry and the dominance of inter- and intraband scattering for odd and even layers of WS2, respectively. The higher demagnetization time, tau m, in 3 and 5 layers of WS2 is indicative of the interaction between spin-orbit and spin-valley coupling due to the broken symmetry. The lower tau m in even layers as compared to the bare FM layer suggests the presence of a spin transport. By correlating tau m and alpha, we pinpointed the dominant mechanisms of ultrafast demagnetization. The mechanism changes from spin transport to spin-flip scattering for even layers of WS2 with increasing fluence. A fundamental understanding of the two-dimensional material and its odd-even layer dependence at ultrashort timescales provides valuable information for designing next-generation spin-based devices. Odd-even WS2 layer number dependent ultrafast demagnetization and damping are studied by varying the pump fluence.
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| 5. |
- Forslund, Ola Kenji, et al.
(författare)
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Intertwined magnetic sublattices in the double perovskite compound LaSrNiReO6
- 2020
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Ingår i: Physical Review B. - : American Physical Society. - 2469-9969 .- 2469-9950. ; 102:14
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Tidskriftsartikel (refereegranskat)abstract
- We report a muon spin rotation (μ+SR) study of the magnetic properties of the double perovskite compound LaSrNiReO6. Using the unique length and time scales of the μ+SR technique, we successfully clarify the magnetic ground state of LaSrNiReO6, which was previously deemed as a spin glass state. Instead, our μ+SR results point toward a long-range dynamically ordered ground state below TC=23 K, for which a static limit is foreseen at T=0. Furthermore, between 23K250 K) state. Our results reveal how two separate yet intertwined magnetic lattices interact within the unique double perovskite structure and the importance of using complementary experimental techniques to obtain a complete understanding of the microscopic magnetic properties of complex materials.
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| 6. |
- Ghorai, Sagar, et al.
(författare)
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A setup for direct measurement of the adiabatic temperature change in magnetocaloric materials
- 2023
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Ingår i: IEEE Transactions on Instrumentation and Measurement. - : Institute of Electrical and Electronics Engineers (IEEE). - 0018-9456 .- 1557-9662. ; 72, s. 1-9
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Tidskriftsartikel (refereegranskat)abstract
- In order to find a highly efficient, environmentally-friendly magnetic refrigerant, direct measurements of the adiabatic temperature change ΔTadb are required. Here, in this work, a simple setup for the ΔTadb measurement is presented. Using a permanent magnet Halbach array with a maximum magnetic field of 1.8 T and a rate of magnetic field change of 5 T/s, accurate determination of ΔTadb is possible in this system. The operating temperature range of the system is from 100 to 400 K, designed for the characterization of materials with potential for room temperature magnetic refrigeration applications. Using the setup, ΔTadb of a first-order and two second-order compounds have been studied. Results from the direct measurement for the first-order compound have been compared with ΔTadb calculated from the temperature and magnetic field-dependent specific heat data. By comparing results from direct and indirect measurements, it is concluded that for a reliable characterization of the magnetocaloric effect (MCE), direct measurement of ΔTadb should be adopted.
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| 7. |
- Ghorai, Sagar
(författare)
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Direct and indirect magnetocaloric properties of first- and second-order phase transition materials
- 2022
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Doktorsavhandling (övrigt vetenskapligt/konstnärligt)abstract
- The energy-efficient and environmentally friendly alternative cooling technology based on the magnetocaloric effect (MCE) is discussed in this thesis. The thesis has two major parts, one devoted to material characterization and the other to instrument development. Different magnetic oxides and intermetallic compounds with second-order and first-order magnetic transitions, respectively, were studied with the aim of finding materials suitable for magnetic refrigeration. For the application of the MCE, a high value of the isothermal entropy changes and the relative cooling power (RCP), along with minimal temperature hysteresis are required. The temperature hysteresis is negligible for all studied second-order compounds, while an almost ten times higher value of the isothermal entropy change has been observed for the first-order compounds. The highest value of isothermal entropy change (20 J/kgK at 2 T applied magnetic field) has been observed for the MnNiSi-type compounds exhibiting magneto-structural phase transitions, while the largest value of the RCP (176 J/kg at 2 T applied magnetic field) has been observed for the Fe2P-type compounds exhibiting magneto-elastic phase transitions.For the characterization of magnetocaloric properties, one important parameter is the adiabatic temperature change, which is often not reported in literature owing to the lack of experimental setups for direct measurements of the magnetocaloric effect. This thesis also includes the development of a setup for the direct measurement of the adiabatic temperature change upon a change in a magnetic field.
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| 8. |
- Ghorai, Sagar, et al.
(författare)
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Effect of reduced local lattice disorder on the magnetic properties of B-site substituted La0.8Sr0.2MnO3
- 2021
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Ingår i: Journal of Magnetism and Magnetic Materials. - : Elsevier. - 0304-8853 .- 1873-4766. ; 529
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Tidskriftsartikel (refereegranskat)abstract
- Disorder induced by chemical inhomogeneity and Jahn-Teller (JT) distortions is often observed in mixed valence perovskite manganites. The main reasons for the evolution of this disorder are connected with the cationic size differences and the ratio between JT active and non-JT active ions. The quenched disorder leads to a spin-cluster state above the magnetic transition temperature. The effect of Cu, a B-site substitution in the La0.8Sr0.2MnO3 compound, on the disordered phase has been addressed here. X-ray powder diffraction reveals rhombohedral (R-3c) structures for both the parent and B-site substituted compound with negligible change of lattice volume. The chemical compositions of the two compounds were verified by ion beam analysis technique. With the change of electronic bandwidth, the magnetic phase transition temperature has been tuned towards room temperature (318 K), an important requirement for room temperature magnetic refrigeration. However, a small decrease of the isothermal entropy change was observed with Cu-substitution, related to the decrease of the saturation magnetization.
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| 9. |
- Ghorai, Sagar, et al.
(författare)
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Effect of small cation occupancy and anomalous Griffiths phase disorder in nonstoichiometric magnetic perovskites
- 2022
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Ingår i: Journal of Alloys and Compounds. - : Elsevier. - 0925-8388 .- 1873-4669. ; 895
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Tidskriftsartikel (refereegranskat)abstract
- The structural, magnetic, magnetocaloric and Griffiths phase (GP) disorder of non-stoichiometric perovskite manganites La0.8-xSr0.2-yMn1+x+yO3 are reported here. Determination of valence states and structural phases evidenced that the smaller cations Mn2+ and Mn3+ will not occupy the A-site of a perovskite under atmospheric synthesis conditions. The same analysis also supports that the vacancy in the A-site of a perovskite induces a similar vacancy in the B-site. The La3+ and Sr2+ cation substitutions in the A-site with vacancy influences the magnetic phase transition temperature (TC) inversely, which is explained in terms of the electronic bandwidth change. An anomalous non-linear change of the GP has been observed in the Sr substituted compounds. The agglomeration of Mn3+-Mn4+ pairs (denoted as dimerons), into small ferromagnetic clusters, has been identified as the reason for the occurrence of the GP. A threshold limit of the dimeron formation explains the observed non-linear behaviour of the GP formation. The Sr-substituted compounds show a relatively large value of isothermal entropy change (maximum 3.27 J/kgK at mu H-0 = 2T) owing to its sharp magnetic transition, while the broad change of magnetization in the La-substituted compound enhances the relative cooling power (maximum 98 J/kg at mu H-0 = 2T).
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| 10. |
- Ghorai, Sagar, et al.
(författare)
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Evolution of Griffiths phase and critical behaviour of La1-xPbxMnO3 +/- y solid solutions
- 2021
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Ingår i: Journal of Physics. - : Institute of Physics Publishing (IOPP). - 0953-8984 .- 1361-648X. ; 33:14
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Tidskriftsartikel (refereegranskat)abstract
- Polycrystalline La1-xPbxMnO3 +/- y (x = 0.3, 0.35, 0.4) solid solutions were prepared by solid state reaction method and their magnetic properties have been investigated. Rietveld refinement of x-ray powder diffraction patterns showed that all samples are single phase and crystallized with the rhombohedral structure in the R-3c space group. A second order paramagnetic to ferromagnetic (FM) phase transition was observed for all materials. The Griffiths phase (GP), identified from the temperature dependence of the inverse susceptibility, was suppressed by increasing magnetic field and showed a significant dependence on A-site chemical substitution. The critical behaviour of the compounds was investigated near to their Curie temperatures, using intrinsic magnetic field data. The critical exponents (beta, gamma and delta) are close to the mean-field approximation values for all three compounds. The observed mean-field like behaviour is a consequence of the GP and the formation of FM clusters. Long-range FM order is established as the result of long-range interactions between FM clusters. The magnetocaloric effect was studied in terms of the isothermal entropy change. Our study shows that the material with the lowest chemical substitution (x = 0.3) has the highest potential (among the three compounds) as magnetic refrigerant, owing to its higher relative cooling power (258 J kg(-1) at 5 T field) and a magnetic phase transition near room temperature.
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