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The cyclotron driven fast quasi-monoenergetic neutron source based on the p+ 9Be (thin target) reaction was studied at the proton energy around 30 MeV Due to higher melting point of Be, the p+ 9Be(thin), reaction could be considered as an alternative to the most used p+Li(thin) neutron source, providing a similar quasi-monoenergetic neutron spectrum at significantly higher neutron output owing to advance in higher incident proton beam current. The neutron spectrum measured by the time-of-flight method agrees with other experimental data and indicates dominant contribution of ground and first excited states leading to only two peaks, separated by some 2–3 MeV, in the p+thin 9Be neutron spectrum.

Numerous domains, in fundamental research as well as in applications, require the study of reactions induced by neutrons with energies from few MeV up to few tens of MeV. Reliable measurements also are necessary to improve the evaluated databases used by nuclear transport codes. This energy range covers a large number of topics like transmutation of nuclear waste, design of future fission and fusion reactors, nuclear medicine or test and development of new detectors. A new facility called Neutrons For Science (NFS) is being built for this purpose on the GANIL site at Caen (France). NFS is composed of a pulsed neutron beam for time-of-flight facility as well as irradiation stations for cross-section measurements. Neutrons will be produced by the interaction of deuteron and proton beams, delivered by the SPIRAL-2 linear accelerator, with thick or thin converters made of beryllium or lithium. Continuous and quasi-mono-energetic spectra will be available at NFS up to 40 MeV. In this fast energy region, the neutron flux is expected to be up to 2 orders of magnitude higher than at other existing time-of-flight facilities. In addition, irradiation stations for neutron-, proton- and deuteron-induced reactions will allow performing cross-section measurements by the activation technique. After a description of the facility and its characteristics, the experiments to be performed in the short and medium term will be presented.

The cyclotron-based fast neutron source at NPI produces mono-energetic neutron fields up to 35 MeV neutron energy using the p + 7Li(carbon backing) reactions. To be applied for activation cross-section measurements, not only the intensity of neutron peak, but also the contribution of low-energy continuum in the spectra must be well determined. Simulations of the spectral flux from present source at a position of irradiated samples were performed using CYRIC TOF-data validated in the present work against LA150h by calculations with the transport Monte Carlo code MCNPX. Simulated spectra were tested by absolute measurements using a proton-recoil telescope technique. The recoil-proton spectrometer consisted of a shielded scattering chamber with polyethylene and carbon radiators and the ΔE1-ΔE2-E telescope of silicon-surface detectors located to the neutron beam axis at 45° in the laboratory system. Si-detectors were handled by usual data acquisition system. Dead-time – and pulse-overlap losses of events were determined from the count rate of pulse generator registered during duty cycle of accelerator operation. The proton beam charge and data were taken in the list mode for later replay and analysis. The calculations for 7Li(p,n) and 12C(p,n) reactions reasonably reproduce CYRIC TOF neutron source spectra. The influence of neutron source set-up (proton beam dimensions, 7Li-foil, carbon stopper, cooling medium, target support/chamber and the geometry-arrangement of irradiated sample) on the spectral flux is discussed in details.

The proton and deuteron induced reactions have a great interest for the assessment of induced radioactivity of accelerator components. Such data are needed for estimation of the potential radiation hazard from the accelerating cavities and beam transport elements. Continuing previous irradiation experiments on copper, we provided two short run to obtain cross-section data for 65Cu(d, p)66Cu reaction. We carried out irradiation experiments with the variable-energy cyclotron U-120M of the Nuclear Physics Institute Řež. The stacked-foil technique was utilized. Because of a relatively short half life (T1/2 = 5, 120 min) and a strong annihilation peak, we placed the 1 cm Pb plate between the irradiated sample and the gamma-ray detector to reduce the dead time. The absolute values of cross-sections were calculated from the induced activities measured by the calibrated HPGe detector. The comparison of present results with data of other authors and prediction of different libraries and model calculation is discussed.

Abstract The intensities of γ -rays from the 196m2Au decay adopted in 1998 and 2007 ENSDF evaluations differ up to 20%. Gold samples were irradiated in intensive neutron fluxes with energies up to 35 MeV to produce the isotopes 196Au in all isomeric states. The intensities of gammas from the radioactive decay of the isomer 196m2Au were measured by means of the nuclear γ -ray spectrometry (HPGe detectors) and compared to the existing adopted data. [ABSTRACT FROM AUTHOR]

Dynamic compaction is a soil improvement technique which involves the repeated application of an impact load to a contact area of the soil surface induced by heavy weights. Experimental measurements were prepared for evaluation of the ground wave propagation induced by the rapid impact compaction. Influence of increase of subsoil stiffness during compaction and terrain configuration were investigated. When the shear strength of soil is exceeded during the penetration of the compaction footing, increase of peak particle velocities is slower but still clearly visible along the measurement line. The peak particle velocity is damped by the subsoil below 5 mm s -1 within 40-50 m from the source of excitation. Attenuation radius is affected by the terrain configuration, when terrain elevations cause the increase of acceleration amplitudes. Rigid bodies in the ground, such as foundation structures, could have similar influence. Dominant frequencies are in the interval from 20 to 40 Hz regardless the distance from the source of excitation or the density of the treated subsoil. Obtained results are preferably related to the given boundary conditions. However, wave propagation pattern and change of its characteristics during densification of the subsoil are applicable at another construction sites considering their particularities., (© 2024. The Author(s).)

The coronavirus disease 2019 (COVID-19) pandemic, caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), has prompted great interest in novel broad-spectrum antivirals, including perylene-related compounds. In the present study, we performed a structure-activity relationship analysis of a series of perylene derivatives, which comprised a large planar perylene residue, and structurally divergent polar groups connected to the perylene core by a rigid ethynyl or thiophene linker. Most of the tested compounds did not exhibit significant cytotoxicity towards multiple cell types susceptible to SARS-CoV-2 infection, and did not change the expressions of cellular stress-related genes under normal light conditions. These compounds showed nanomolar or sub-micromolar dose-dependent anti-SARS-CoV-2 activity, and also suppressed the in vitro replication of feline coronavirus (FCoV), also termed feline infectious peritonitis virus (FIPV). Perylene compounds exhibited high affinity for liposomal and cellular membranes, and efficiently intercalated into the envelopes of SARS-CoV-2 virions, thereby blocking the viral-cell fusion machinery. Furthermore, the studied compounds were demonstrated to be potent photosensitizers, generating reactive oxygen species (ROS), and their anti-SARS-CoV-2 activities were considerably enhanced after irradiation with blue light. Our results indicated that photosensitization is the major mechanism underlying the anti-SARS-CoV-2 activity of perylene derivatives, with these compounds completely losing their antiviral potency under red light. Overall, perylene-based compounds are broad-spectrum antivirals against multiple enveloped viruses, with antiviral action based on light-induced photochemical damage (ROS-mediated, likely singlet oxygen-mediated), causing impairment of viral membrane rheology., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023. Published by Elsevier B.V.)

Diphyllin is a natural arylnaphtalide lignan extracted from tropical plants of particular importance in traditional Chinese medicine. This compound has been described as a potent inhibitor of vacuolar (H + )ATPases and hence of the endosomal acidification process that is required by numerous enveloped viruses to trigger their respective viral infection cascades after entering host cells by receptor-mediated endocytosis. Accordingly, we report here a revised, updated, and improved synthesis of diphyllin, and demonstrate its antiviral activities against a panel of enveloped viruses from Flaviviridae, Phenuiviridae, Rhabdoviridae, and Herpesviridae families. Diphyllin is not cytotoxic for Vero and BHK-21 cells up to 100 µM and exerts a sub-micromolar or low-micromolar antiviral activity against tick-borne encephalitis virus, West Nile virus, Zika virus, Rift Valley fever virus, rabies virus, and herpes-simplex virus type 1. Our study shows that diphyllin is a broad-spectrum host cell-targeting antiviral agent that blocks the replication of multiple phylogenetically unrelated enveloped RNA and DNA viruses. In support of this, we also demonstrate that diphyllin is more than just a vacuolar (H + )ATPase inhibitor but may employ other antiviral mechanisms of action to inhibit the replication cycles of those viruses that do not enter host cells by endocytosis followed by low pH-dependent membrane fusion.

The paper describes neutron field characterisation of low-flux multipurpose educational irradiator developed at Czech Technical University in Prague. The irradiator is aimed for demonstration experiments including neutron activation analysis, delayed neutron counting, or studies related to neutron and/or gamma detection and spectrometric devices. It may accommodate various neutron sources including 252 Cf or AmBe radionuclide sources, D-D generator, or in-reactor irradiated nuclear material serving as delayed neutron source, or gamma sources including radionuclide ones or short-lived sources produced in the adjacent reactor. The characterisation was performed based on neutron activation technique using gold foils. It included two experimental parts. The first one verified the level of response symmetry in the four irradiation channels and characterisation of the axial distribution in the irradiation channels. Within the second one, the responses to thermal and epithermal neutrons and the cadmium ratio in the central irradiation position were determined. Whereas the former was determined solely with the 252 Cf source, the latter was performed for all available sources: 252 Cf, AmBe, and the D-D generator. The experimental results were further compared to calculations by the MCNP Monte Carlo code., (Copyright © 2020 Elsevier Ltd. All rights reserved.)

Emerging flaviviruses are causative agents of severe and life-threatening diseases, against which no approved therapies are available. Among the nucleoside analogues, which represent a promising group of potentially therapeutic compounds, fluorine-substituted nucleosides are characterized by unique structural and functional properties. Despite having first been synthesized almost 5 decades ago, they still offer new therapeutic opportunities as inhibitors of essential viral or cellular enzymes active in nucleic acid replication/transcription or nucleoside/nucleotide metabolism. Here, we report evaluation of the antiflaviviral activity of 28 nucleoside analogues, each modified with a fluoro substituent at different positions of the ribose ring and/or heterocyclic nucleobase. Our antiviral screening revealed that 3'-deoxy-3'-fluoroadenosine exerted a low-micromolar antiviral effect against tick-borne encephalitis virus (TBEV), Zika virus, and West Nile virus (WNV) (EC 50 values from 1.1 ± 0.1 μM to 4.7 ± 1.5 μM), which was manifested in host cell lines of neural and extraneural origin. The compound did not display any measurable cytotoxicity up to concentrations of 25 μM but had an observable cytostatic effect, resulting in suppression of cell proliferation at concentrations of >12.5 μM. Novel approaches based on quantitative phase imaging using holographic microscopy were developed for advanced characterization of antiviral and cytotoxic profiles of 3'-deoxy-3'-fluoroadenosine in vitro In addition to its antiviral activity in cell cultures, 3'-deoxy-3'-fluoroadenosine was active in vivo in mouse models of TBEV and WNV infection. Our results demonstrate that fluoro-modified nucleosides represent a group of bioactive molecules with excellent potential to serve as prospective broad-spectrum antivirals in antiviral research and drug development., (Copyright © 2021 American Society for Microbiology.)

197Au, 209Bi, 59Co, natFe and 169Tm samples were irradiated several times with quasi-monoenergetic neutrons from the p+7Li reaction in the energy range of 18-34 MeV. The activities of the samples were measured with the HPGe detector and the reaction rates were calculated. The cross sections were extracted using the SAND-II code with the reference cross sections from the IRDFF database.

The neutrons for science (NFS) facility is a component of SPIRAL-2, the new superconducting linear accelerator built at GANIL in Caen (France). The proton and deuteron beams delivered by the accelerator will allow producing intense neutron fields in the 100 keV-40 MeV energy range. Continuous and quasi-mono-kinetic energy spectra, respectively, will be available at NFS, produced by the interaction of a deuteron beam on a thick Be converter and by the 7Li(p,n) reaction on thin converter. The pulsed neutron beam, with a flux up to two orders of magnitude higher than those of other existing time-of-flight facilities, will open new opportunities of experiments in fundamental research as well as in nuclear data measurements. In addition to the neutron beam, irradiation stations for neutron-, proton- and deuteron-induced reactions will be available for cross-sections measurements and for the irradiation of electronic devices or biological cells. NFS, whose first experiment is foreseen in 2018, will be a very powerful tool for physics, fundamental research as well as applications like the transmutation of nuclear waste, design of future fission and fusion reactors, nuclear medicine or test and development of new detectors.

A well-defined neutron spectrum is an essential tool not only for calibration and testing of neutron detectors used in dosimetry and spectroscopy but also for validation and verification of evaluated cross sections. A new evaluation of thermal-neutron induced 235 U PFNS was performed by the International Atomic Energy Agency (IAEA) in the CIELO (Collaborative International Evaluated Library Organisation Project) project; new measurements of Spectral Averaged Cross sections averaged in the evaluated spectrum are to be obtained. In general, a neutron spectrum in the core is not identical to the pure fission one because fission neutrons undergo many scattering reactions, but it can be shown that PFNS and reactor spectra become undistinguishable from a certain energy boundary. This limit is important for experiments, because when the studied reaction threshold is over this limit, the spectral averaged cross sections in PFNS can be derived from the measured reactions in the reactor core. The evaluation of the neutron spectrum measurements in three different thermal-reactor cores shows that this lower limit is around the energy of 5.5 - 6 MeV. Above this energy the reactor spectra becomes identical with the 235 U PFNS. IAEA CIELO PFNS is within 5% of the measured PFNS from 10 to 14 MeV in a LR-0 reactor, while ENDF/B-VII evaluated PFNS underestimated measured neutron spectra., (Copyright © 2018 Elsevier Ltd. All rights reserved.)

Arthropod-borne flaviviruses are human pathogens of global medical importance, against which no effective small molecule-based antiviral therapy has currently been reported. Arbidol (umifenovir) is a broad-spectrum antiviral compound approved in Russia and China for prophylaxis and treatment of influenza. This compound shows activities against numerous DNA and RNA viruses. The mode of action is based predominantly on impairment of critical steps in virus-cell interactions. Here we demonstrate that arbidol possesses micromolar-level anti-viral effects (EC 50 values ranging from 10.57 ± 0.74 to 19.16 ± 0.29 µM) in Vero cells infected with Zika virus, West Nile virus, and tick-borne encephalitis virus, three medically important representatives of the arthropod-borne flaviviruses. Interestingly, no antiviral effects of arbidol are observed in virus infected porcine stable kidney cells (PS), human neuroblastoma cells (UKF-NB-4), and human hepatoma cells (Huh-7 cells) indicating that the antiviral effect of arbidol is strongly cell-type dependent. Arbidol shows increasing cytotoxicity when tested in various cell lines, in the order: Huh-7 < HBCA < PS < UKF-NB-4 < Vero with CC 50 values ranging from 18.69 ± 0.1 to 89.72 ± 0.19 µM. Antiviral activities and acceptable cytotoxicity profiles suggest that arbidol could be a promising candidate for further investigation as a potential therapeutic agent in selective treatment of flaviviral infections., Competing Interests: The authors declare that they have no competing interests.

There are currently no approved antiviral therapies against medically important human flaviviruses. The imino-C-nucleoside BCX4430 shows broad-spectrum antiviral activity against a wide range of RNA viruses. Here, we demonstrate that BCX4430 inhibits tick-borne species of the genus Flavivirus; however, the antiviral effect varies against individual species. Micro-molar BCX4430 levels inhibited tick-borne encephalitis virus (TBEV); while, approximately 3-8-fold higher concentrations were needed to inhibit louping ill virus and Kyasanur Forest disease virus. Moreover, the compound strongly inhibited in vitro replication of West Nile virus, a typical mosquito-transmitted flavivirus. Two chemical forms of the compound, i.e. BCX4430 and BCX4430 hydrochloride, were compared and both exerted similar inhibitory profiles in our in vitro antiviral assay systems and no or negligible cytotoxicity in porcine kidney stable and Vero cells. The obtained data indicate that, in addition to mosquito-borne flaviviruses, the compound has strong antiviral activity against members of the TBEV serocomplex., (Copyright © 2017 Elsevier B.V. All rights reserved.)