Search Results (9)

Flavonoids, natural organic compounds from the polyphenolic group with broad bioactive and pharmaceutical properties, are strong ligands for many metal ions. This work describes the formation of the complex between Zn(II) and morin. The synthesized compound is characterized using three analytical techniques, i.e., ¹H NMR, IR, and thermal gravimetric analysis. Importantly, the complex was successfully obtained in the form of a solid, which enables its further physicochemical and structural characterization. Physicochemical characterization of the Morin-Zn complex was performed by steady-state and time-resolved spectroscopy. The absorption spectrum of the complex contains two main bands at ca. 407–415 nm and ca. 265 nm, and the complex emits yellow-green light with higher intensity than the free ligand. In the next step, morin and zinc complex were dispersed in a PMMA (poly (methyl methacrylate)) polymer matrix, and respective thin layers were produced. The studied thin films were deposited on silicon substrates by using the spin-coating method and characterized by X-ray photoelectron spectroscopy (XPS), Atomic Force Microscopy (AFM), Spectroscopic Ellipsometry (SE), UV-VIS spectroscopy, and photoluminescence (PL). The absorption of thin layers showed, similarly to solutions, the presence of two transitions: π→π* and n→π*, and a bathochromic shift for the morin-zinc complex compared to morin. The photoluminescence of the complex thin film showed two bands, the first in the range of 380–440 nm corresponding to PMMA, and the second with a maximum at 490 nm, derived from the synthesized compound. Full article

Non-small-cell lung cancer (NSCLC) remains the leading cause of cancer-related deaths globally, with a persistently low five-year survival rate of only 14–17%. High rates of metastasis contribute significantly to the poor prognosis of NSCLC, in which inflammation plays an important role by enhancing tumor growth, angiogenesis, and metastasis. Targeting inflammatory pathways within cancer cells may thus represent a promising strategy for inhibiting NSCLC metastasis. This study evaluated the anti-inflammatory and anti-metastatic properties of morin, a bioactive compound derived from a Thai medicinal herb, focusing on its effects on NLRP3 inflammasome-mediated pathways in an in vitro NSCLC model. The A549 and H1299 cell lines were stimulated with lipopolysaccharide (LPS) and adenosine triphosphate (ATP) to activate the NLRP3 pathway. The inhibition effects exhibited by morin in reducing pro-inflammatory secretion in LPS- and ATP-stimulated NSCLC cells were assessed by ELISA, while wound healing and trans-well invasion assays evaluated its impact on cell migration and invasion. RT-qPCR measurement quantified the expression of inflammatory genes, and zymography and Western blotting were used to examine changes in invasive protein levels, epithelial-to-mesenchymal transition (EMT) markers, and underlying molecular mechanisms. Our findings demonstrated the significant ability of morin to decrease the production of IL-1β, IL-18, and IL-6 in a dose-dependent manner (p < 0.05), as well as suppress NSCLC cell migration and invasion. Morin downregulated invasive proteins (MMP-2, MMP-9, u-PAR, u-PA, MT1-MMP) and EMT markers (fibronectin, N-cadherin, vimentin) (p < 0.01) while also reducing the mRNA levels of NLRP3, IL-1β, IL-18, and IL-6. Mechanistic investigations revealed that morin suppressed NLRP3 inflammasome activity and inactivated MAPK pathways. Specifically, it decreased the expression of NLRP3 and ASC proteins and reduced caspase-1 activity, while reducing the phosphorylation of ERK, JNK, and p38 proteins. Collectively, these findings suggest that morin’s inactivation of the NLRP3 inflammasome pathway could offer a novel therapeutic strategy for counteracting pro-tumorigenic inflammation and metastatic progression in NSCLC. Full article

The inherent existence of multi phases in iron oxide nanostructures highlights the significance of them being investigated deliberately to understand and possibly control the phases. Here, the effects of annealing at 250 °C with a variable duration on the bulk magnetic and structural properties of high aspect ratio biphase iron oxide nanorods with ferrimagnetic Fe₃O₄ and antiferromagnetic α-Fe₂O₃ are explored. Increasing annealing time under a free flow of oxygen enhanced the α-Fe₂O₃ volume fraction and improved the crystallinity of the Fe₃O₄ phase, identified in changes in the magnetization as a function of annealing time. A critical annealing time of approximately 3 h maximized the presence of both phases, as observed via an enhancement in the magnetization and an interfacial pinning effect. This is attributed to disordered spins separating the magnetically distinct phases which tend to align with the application of a magnetic field at high temperatures. The increased antiferromagnetic phase can be distinguished due to the field-induced metamagnetic transitions observed in structures annealed for more than 3 h and was especially prominent in the 9 h annealed sample. Our controlled study in determining the changes in volume fractions with annealing time will enable precise control over phase tunability in iron oxide nanorods, allowing custom-made phase volume fractions in different applications ranging from spintronics to biomedical applications. Full article

Morin (M) is one of the most widely distributed flavonoids with several beneficial effects on human health, and has the potential of being used as a possible treatment for COVID-19. To achieve a better understanding of the process of M dissolution, the fluorescent (FL) emission from M solutions prepared with different polar and nonpolar solvents (methanol, DMSO, and chloroform) was measured and compared with the FL emission from M powder and M crystals. In the FL spectra of the solutions with high M concentration, as well as in the spectra of M in solid state, two features, at 615 nm and 670 nm, were observed. As the solution concentration decreases, the maxima of FL spectra of the M solutions in all considered solvents shift to the blue side of the spectrum until reaching the value of 520 nm. To explain the experimental results, the TDDFT-M06-2X/6-31++G(d,p) method was used to determine the possible electronic transitions in the M molecule. The computations show that the FL emission in the spectral range of detection of our setup (405–800 nm) is related to the excited state intramolecular proton transfer (ESIPT). Comparison of the experimental data with the computations strongly suggests that in low-concentrated solutions, the FL emission is mostly due to electronic transitions in the keto OH3 form, whereas in aggregated states, the dominate contribution to the FL emission spectra is due to the transitions in keto OH5 form. Moreover, the time evolution of the M solutions FL spectra was observed, measured and explained for the first time. Full article

A temperature-dependent Raman experiment between 80 and 600 K was performed in a nanoparticulated coating of single-phase hematite grown on a silica substrate. In that range, a thermal Raman shift hysteresis was identified in the vibrational modes that accompanies the Morin transition, observing large effects in the two-magnon Raman frequency position and in its relative intensity. Interestingly, no decrease in coercivity occurs when the hematite crosses the Morin transition below 230 K. The spin-flop processes produced in the coating leads to a strong decompensation of the surface spins, generating a ferromagnetic component over the whole temperature range studied. Such unusual effects might be promoted by a certain degree of structural disorder and the stresses produced by the nanoparticulation growth approach of the hematite coating. As a result, a high stability of the two-magnon excitation is obtained over a wide temperature range and considerable advances are made for the development of spintronic devices based on semiconductor antiferromagnetic materials. Full article

MoO₂-Fe₂O₃ nanoparticle systems were successfully synthesized by mechanochemical activation of MoO₂ and α-Fe₂O₃ equimolar mixtures throughout 0–12 h of ball-milling. The role of the long-range ferromagnetism of MoO₂ on a fraction of more defect hematite nanoparticles supporting a defect antiferromagnetic phase down to the lowest temperatures was investigated in this work. The structure and the size evolution of the nanoparticles were investigated by X-ray diffraction, whereas the magnetic properties were investigated by SQUID magnetometry. The local electronic structure and the specific phase evolution in the analyzed system versus the milling time were investigated by temperature-dependent Mössbauer spectroscopy. The substantially shifted magnetic hysteresis loops were interpreted in terms of the unidirectional anisotropy induced by pinning the long-range ferromagnetic order of the local net magnetic moments in the defect antiferromagnetic phase, as mediated by the diluted magnetic oxide phase of MoO₂, to those less defect hematite nanoparticles supporting Morin transition. The specific evolutions of the exchange bias and of the coercive field versus temperature in the samples were interpreted in the frame of the specific phase evolution pointed out by Mössbauer spectroscopy. Depending on the milling time, a different fraction of defect hematite nanoparticles is formed. Less nanoparticles supporting the Morin transition are formed for samples exposed to a longer milling time, with a direct influence on the induced unidirectional anisotropy and related effects. Full article

Mesoproterozoic magnesite deposits are found associated with dolomitic marble and intercalated with metasedimentary rocks of the Grenville Supergroup in the granulite facies Morin terrane (Grenville Province, Quebec). This study examines one of the remaining ore deposits exposed on the surface (at the Dobbie mine), and presents stable isotope and mineralogical data for a marine evaporitic origin. The magnesite ore zone has δ¹⁸O(Mag) = 25.5 ± 0.4‰ (VSMOW) and δ¹³C(Mag) = 1.7 ± 0.2‰ (VPDB; n = 7), while surrounding dolomitic marble has δ¹⁸O(Dol) = 24.2 ± 0.6‰ and δ¹³C(Dol) = −0.2 ± 0.7‰ (n = 11). These values are at the high end of the range for other Morin terrane marbles, and this and sharp transitions in stable isotope ratios between lithologies argue for preservation of evaporitic enrichment in δ¹⁸O and δ¹³C. Boron isotope ratios (δ¹¹B = 15.5‰ to 22.7‰) are also consistent with a marine evaporite origin. Identifying evaporitic protoliths in metasedimentary rocks is important for determining pre-metamorphic depositional environments, and in this case links the sedimentary setting of the Morin terrane to the Adirondack Lowlands (New York, NY, USA). The identification of the Kilmar magnesite deposits as evaporitic also has implications for the formation of sedimentary exhalative base metal deposits in the Grenville Supergroup. Full article

Spectra of quantum beats (QBs) of nuclear resonant forward scattering contain the interference information of all allowed energy transitions of a nucleus, which makes it complicated to extract hyperfine structure directly. Here, we propose a new method, based upon the extraction of prime beat components, to understand QBs. In this method, the origin of major spectral lines in the Fourier Transformation of QBs is studied, and the energy levels of hyperfine structure are obtained directly from the QBs. We applied this method to the temperature dependent QBs of hematite. The Morin temperature and hyperfine structure obtained by this method are in consistent with that by conventional Mössbauer spectroscopy (MS). It serves to interpret the components of QBs of nuclear resonant forward scattering as simple as the conventional (MS). Full article

Iron oxide nanoparticles are widely prevalent in our aqueous environment (e.g., streams, seawater, hydrothermal vents). Their aggregation and crystal growth depend on their chemical surroundings, for instance just a change in pH or salt concentration can greatly affect this. In turn this influences their properties, mobility, fate, and environmental impact. We studied the growth of α-Fe₂O₃ (hematite), starting from 8 nm hematite particles in weakly acidic (HNO₃) aqueous suspension with different states of particle aggregation, using salt (NaCl and NaH₂PO₄) to control their initial aggregation state. The samples were then subject to hydrothermal treatment at 100–140 °C. We followed the development in aggregation state and particle size by dynamic light scattering, X-ray diffraction, small angle neutron scattering and transmission electron microscopy, and the magnetic properties by Mössbauer spectroscopy. The addition of NaCl and NaH₂PO₄ both led to aggregation, but NaCl led to linear chains of hematite nanoparticles (oriented parallel to their hexagonal c-axis), such that the crystalline lattice planes of neighboring hematite particles were aligned. However, despite this oriented alignment, the particles did not merge and coalesce. Rather they remained stable as mesocrystals until heat-treated. In turn, the addition of NaCl significantly increases the rate of growth during hydrothermal treatment, probably because the nanoparticles, due to the chain formation, are already aligned and in close proximity. With hydrothermal treatment, the magnetic properties of the particles transform from those characteristic of small (aggregated) hematite nanoparticles to those of particles with more bulk-like properties such as Morin transition and suppression of superparamagnetic relaxation, in correspondence with the growth of particle size. Full article