Electron Spin Resonance Spectrometer Research Articles

Protective effect of luteolin against oxidative stress‑mediated cell injury via enhancing antioxidant systems.

Physiological stress such as excessive reactive oxygen species (ROS) production may contribute normal fibroblasts activation into cancer‑associated fibroblasts, which serve a crucial role in certain types of cancer such as pancreatic, breast, liver and lung cancer. The present study aimed to examine the cytoprotective effects of luteolin (3',4',5,7‑tetrahydroxyflavone) against hydrogen peroxide (H2O2)‑generated oxidative stress in lung fibroblasts. To examine the effects of luteolin against H2O2‑induced damages, cell viability, sub‑G1 cell population, nuclear staining with Hoechst 33342, lipid peroxidation and comet assays were performed. To evaluate the effects of luteolin on the protein expression level of apoptosis, western blot assay was performed. To assess the antioxidant effects of luteolin, detection of ROS using H2DCFDA staining, O2‑ and ·OH using electron spin resonance spectrometer and antioxidant enzyme activity was performed. In a cell‑free chemical system, luteolin scavenges superoxide anion and hydroxyl radical generated by xanthine/xanthine oxidase and the Fenton reaction (FeSO4/H2O2). Furthermore, Chinese hamster lung fibroblasts (V79‑4) treated with H2O2 showed a significant increase in cellular ROS. Intracellular ROS levels and damage to cellular components such as lipids and DNA in H2O2‑treated cells were significantly decreased by luteolin pretreatment. Luteolin increased cell viability, which was impaired following H2O2 treatment and prevented H2O2‑mediated apoptosis. Luteolin suppressed active caspase‑9 and caspase‑3 levels while increasing Bcl‑2 expression and decreasing Bax protein levels. Additionally, luteolin restored levels of glutathione that was reduced in response to H2O2. Moreover, luteolin enhanced the activity and protein expressions of superoxide dismutase, catalase, glutathione peroxidase, and heme oxygenase‑1. Overall, these results indicated that luteolin inhibits H2O2‑mediated cellular damage by upregulating antioxidant enzymes.

Effects of dissolved organic matter from sludge pyrolysis biochar on the triclosan removal from contaminated soil

When sludge biochar (SC) prepared from sewage sludge was used to remove triclosan (TCS) from both aqueous solution and soil, the adsorption capacity increased with increasing pyrolysis temperature, while the degradation rate showed a different pattern, namely, SC-500 > SC-800 > SC-600 > SC-700. TCS degradation rate achieved nearly 100 % at 2 h with SC-500 used as a Fenton catalyst. Aromaticity of dissolved organic matter (DOM) was positively correlated with the degradation of TCS and adding homologous DOM solution shortened the equilibrium time of TCS degradation, while removing DOM from SC prolonged, compared to the original SC. The results of X-ray photoelectron spectroscopy (XPS) and electron paramagnetic resonance spectrometer (EPR) characterization indicated that SC-500 performed a stronger catalytic degradation ability due to the relatively high Fe2+ content to produce more ∙OH and SC-derived DOM act as an electron shuttle to promote other reactive oxidative species generation through two free radical pathways in the activation of H2O2 by Fe2+, which in turn promoted the degradation of TCS.

Free radical production induced by visible light in live fruit flies

Visible light triggers free radical production in alive and intact Drosophila melanogaster. We exposed fruit flies to red (613–631 nm), green (515–535 nm), and blue (455–475 nm) light while we monitored changes in unpaired electron content with an electron spin resonance spectrometer (ESR/EPR). The immediate response to light is a rapid increase in spin content lasting approximately 10 s followed by a slower, linear increase for approximately 170 s. When the light is turned off, the spin population promptly decays with a similar time course, though never fully returning to baseline. The magnitude and time course of the spin production depends on the wavelength of the light. Initially, we surmised that eumelanin might be responsible for the spin change because of its documented ability for visible light absorption and its highly stable free radical content. To explore this, we utilized different fruit fly strains with varying eumelanin content and clarified the relation of melanin types with the spin response. Our findings revealed that flies with darker cuticle have at least three-fold more unpaired electrons than flies with yellow cuticle. However, to our surprise, the increase in unpaired electron population by light was not drastically different amongst the genotypes. This suggests that light-induced free radical production may not exclusively rely on the presence of black melanin, but may instead be dependent on light effects on quinone-based cuticular polymers.

Efficient removal of size-fractionated antibiotic resistance genes (ARGs) in WWTPs secondary effluent by vacuum ultraviolet (VUV) activated potassium peroxymonosulfate (PMS)

Antibiotic resistance genes (ARGs) and mobile genetic elements (MGEs) in secondary effluent from wastewater treatment plants (WWTPs) have a size-fractionated character and conventional processes have difficulties in removing ARGs and MGEs. Therefore, this study aimed to explore the removal efficiency, removal mechanism and regeneration potential of size-fractionated ARGs and MGEs by vacuum ultraviolet (VUV)-activated peroxymonosulfate (PMS) and ascertain their potential hosts in secondary effluent. The proportion of particle-associated (PA)-ARGs and PA-MGEs was 85.07 %, followed by free-living (FL) fraction (14.91 %) and cell-free (CF) fraction (0.02 %). More than 95.00 %∼99.99 % of ARGs and MGEs in PA- and CF- fractions were removed by VUV/PMS, but the average removal efficiency of FL-ARGs and FL-MGEs was 66.15 %. Compared to the regeneration potential of PA- and CF-ARGs and MGEs (0.02 < C/C0 < 5.27), the regeneration occurred mainly in FL-ARGs and FL-MGEs (0.08 < C/C0 < 24.06). ·OH was the dominant radical (16.810 × 10-6 mol/L) in VUV/PMS for the removal of size-fractionated ARGs and MGEs from the secondary effluent, while SO4-· (4.478 × 10-6 mol/L) played a supporting role in the system based on the quenching experiment, electron paramagnetic resonance spectrometer and probe experiments. Based on full-scale classification, conditionally rare or abundant taxa (CRAT) were the core potential hosts in PA-, FL- and CF- fractions, while rare taxa (RT) and conditionally rare taxa (CRT) potential hosts were more diverse in the three fractions. This study suggests that VUV/PMS can effectively remove size-fractionated ARGs and MGEs from secondary effluent and thereby obviously reduce their dissemination risk to receiving water bodies, providing technical support for the engineering application of VUV/PMS in full-scale WWTPs.

Designing unimolecular photoinitiator by installing NHPI esters along the TX backbone for acrylate photopolymerization and their applications in coatings and 3D printing

Developing efficient and long wavelength sensitive unimolecular photoinitiators (PIs) is still facing a great challenge. In this work, a series of thioxanthone-based N-hydroxyphthalimide esters (TX-NHPIEs) were synthesized by installing NHPIEs along the TX backbone and characterized. The investigated TX-NHPIEs have a 60 nm redshift and demonstrate sterling initiating efficiency for free radical photopolymerization (FRP) under LED@450 nm light irradiation compared with the commercialized isopropylthioxanthone (ITX). Real-time 1Hnuclear magnetic resonance (1H NMR), electron spin resonance (ESR), decarboxylation and gas chromatograph-mass spectrometer (GC–MS) experiments and density functional theory (DFT) reveal that TX-NHPIEs can generate one alkyl radical and one N-centered iminyl radical, which can initiate FRP directly and indirectly, respectively. In other words, TX-NHPIEs absorb one photon and can generate two active radicals, which break through the limitations of common PIs. TX-NHPIE-Cpe demonstrates the highest initiating efficiency, and its application in coatings and 3D printing was also studied, indicating TX-NHPIEs have broad potential applications in photopolymerization processes.

The study of dosimetric properties of sulfanilic acid in low radiation dose range using the ESR technique

The development of new dosimeters with good dosimetric properties is important for quality control in radiation applications. In this study, the potential of sulfanilic acid (C6H7NO3S) powder form, as a dosimeter in low-dose ionizing radiation (<30 Gy), was analyzed by an Electron Spin Resonance spectrometer (Bruker EMX-131 X-band). Gamma irradiations were performed at room temperature (290 K) using a 60Co gamma cell supplying a dose rate of 32 Gy/h and X photon irradiations at 6 and 18 MV energies were performed using a variant DHX model clinical linear accelerator (Linac) at a dose rate of 3 Gy/min. While unirradiated (control) sulfanilic acid exhibited no ESR signal, the irradiated sample showed a single-line ESR spectrum spread over a magnetic field range of 100 G, as shown in Figure 2. Variations of the peak heights with the sample mass irradiated at 2 Gy gamma dose were studied in the range of 130–330 mg. The ESR signal intensity observed at g-factor = 2.0053 of this compound is dependent on sample mass, so ∼250 mg was chosen at each step of the study. The paramagnetic center formed in the gamma-irradiated sulfanilic acid was followed over 50 days. The dose-response curves were given in the dose range from 0.05 to 10 Gy for the sample exposed to gamma radiation and for the sample exposed in the range of 0.05 Gy–30 Gy at 6 and 18 MV X-ray energies. The fitting values of the function that best describes dose-response curves are calculated. In the g value region, where the ESR signal was observed in the irradiated sample, the lowest dose value at which the signal could be read was 50 mGy, significantly different from the noise. With all these investigations, sulfanilic acid can be used to estimate gamma radiation dose within boundary conditions in medical applications.

Study of Photodegradation of Thiazion Dye Methylene Blue under Exposure to a Laser for Photodynamic Therapy

Purpose. To study the process of photodegradation of methylene blue under the influence of laser radiation with a wavelength of 660 nm, used for photodynamic therapy installations, for the formation of reactive oxygen species, in particular short-lived hydroxyl radicals, using electron paramagnetic resonance (EPR) spectroscopy.Methods. The residual concentration of methylene blue during photodegradation was determined using an HR2000 spectrometer. The formation of hydroxyl groups was detected using an EPR spectrometer SPINSCAN X.Results. Analysis of data on the photodegradation of methylene blue shows that under the influence of laser radiation with a wavelength of 660 nm, the structure of methylene blue is destroyed, manifested in the gradual discoloration of the dye solution. When trypaflavin is added to the solution, the rate of photodegradation of methylene blue slows down significantly. Analysis of ESR spectroscopy data shows that when methylene blue is exposed to a red laser, (OH’) radicals begin to intensively form in the solution. Their content increases significantly with increasing irradiation power.Conclusion. Irradiation of an aqueous solution of the thiazion dye methylene blue by a laser source with a power of 0.3÷1 W and a wavelength of 660 nm leads to its active photodegradation. The addition of trypaflavin leads to a slowdown in the process of photodegradation of methylene blue when irradiated with red light due to the consumption of part of the generated oxygen-containing radicals for the degradation of trypaflavin. According to EPR spectroscopy data using DMPO spin traps, it has been proven that when methylene blue is irradiated with a red laser, active formation of hydroxyl OH' radicals occurs. It was found that with increasing laser radiation intensity, the amount of generated hydroxyl radicals (OH') increases significantly. The presented results may contribute to the development of effective photosensitizers for photodynamic therapy of tumor tumors.

Simple and effective in situ sample illumination for electron paramagnetic resonance.

Illumination into an electron paramagnetic resonance (EPR) spectrometer is commonly carried out through the optical window, perpendicular to the sample and magnetic field. Here we show that significant improvements can be obtained by using the walls of the EPR tube as a light guide, with the light scattered only around the sample-containing area.

Understanding the Reaction Mechanism and Kinetics of Mediated Li-O2 Batteries Using Flow Set-Ups and Cyclic Voltammetry

Li-O2 batteries are very promising candidates for electromobility because of their very high theoretical energy density. Moreover, they are composed of abundant materials, as opposed to Li-ion batteries, which would make them a greener and cheaper alternative. The principal reaction in Li-O2 batteries is the formation of lithium peroxide during discharge via the oxygen reduction reaction (ORR), that is then oxidised during the charge by the oxygen evolution reaction (OER). One of the major challenges of Li-O2 batteries is related to the insulating nature of their discharge product, that significantly limits the capacity and hinders performance. A strategy to overcome this is by using redox mediators (RMs), which shuttle electrons from the electrode surface to the solution and thus facilitate a solution-based mechanism for the formation of large crystals. Understanding the reaction kinetics of these RMs can therefore aid in increasing the battery performance.Quinones, specifically 2,5-Di-tert-butyl-1,4-benzoquinone (DBBQ),is a commonly used discharge RM in this type of batteries. However, their reaction kinetics and how these vary with different electrolyte conditions are not yet well understood. DBBQ undergoes two single electron reductions, whose potentials and kinetics vary with salt concentrations and solvent having a direct effect on its ability to mediate the ORR.In this work, we have developed a Li-O2 flow cell to study the reaction mechanism and kinetics of DBBQ, and performed cyclic voltammetry (CV) studies to better understand how these vary with changing solvent and salt conditions. In the Li-O2 flow set-up the battery is positioned outside the nuclear magnetic resonance (NMR) magnet and plastic tubing then runs through the NMR and electron paramagnetic resonance (EPR) spectrometers. In this way, the reduction of the DBBQ can be monitored while the battery is cycling. In the proton NMR, the neutral DBBQ signals disappear on discharge as the singly reduced DBBQ semiquinone monoanion is a radical. The fast electron exchange between the neutral and radical species broaden out the NMR signals on discharge as the EPR signal grows. On charge, the neutral DBBQ signal reappears and the EPR signal disappears. The Li-O2 flow set-up is very sensitive to air and moisture exposure as the tubing is not perfectly impermeable to them. Therefore, having the CVs as a complementary method to study the reaction mechanisms and kinetics is very useful.We have developed a theoretical framework of Li-coupled electron transfer reactions that can predict the electrochemical kinetics in the presence of high and low donor number solvents and used to quantify thermodynamic and kinetic parameters. We define E0 app and k0 app as the apparent thermodynamic and kinetic parameters that describe the overall system and can be derived from the Nernst equation and Butler Volmer kinetics. These overall descriptors depend on the pathway the reaction takes (Figure 1). The different pathways in different solvents/salts are due to changes in the Li+ solvation strength as well as the competing ionic association of the counter anion.Experimentally, we have shown that in three different solvents, DME, tetraglyme and DMSO the behaviour of DBBQ can be explained by this theoretical framework. In DME, the DBBQ behaviour is most reminiscent of pathway 1 where the kinetics slow down with increasing Li+ concentration. In DMSO the kinetics present a maximum at Li+ concentrations around 1M. Simulations and fitting of the CV experiments in DMSO for the first reduction are in good agreement with pathways 2 and 3, while in tetraglyme it is harder to explain the trends as they do not fit into just one of the pathways.In conclusion we have studied the mechanism and kinetics of DBBQ as a RM for Li-O2 batteries with an in-situ flow set up and CVs and build a theoretical framework to understand how these vary in different electrolyte conditions. This method can be extended to study both the second reduction of DBBQ and other discharge and charge RMs for Li-O2 batteries. Figure 1

First magnetic and spectroscopic constraints on attenuated space weathering at the Chang'e-5 landing site

Space weathering is a primary process altering the lunar surface, producing submicroscopic iron particles embedded in soil grains, which have diagnostic magnetic and spectroscopic effects. However, the space weathering of lunar soils from young geological units remains mysterious without solid constraints from returned samples. Chang'e-5 mission is the first lunar sample-return mission in decades. The Chang'e-5 landing and sampling unit (∼2.0 Ga) is much younger than all Apollo and Luna units (>3.0 Ga). It has provided an unprecedented opportunity to reveal the recent space weathering characteristics with both returned soil samples and in situ investigation data. In this study, magnetic approaches (Vibrating Sample Magnetometer, Electron Paramagnetic Resonance Spectrometer, Mössbauer Spectrometer) were used to characterize the Chang'e-5 lunar soil for the first time after the return of the samples, strongly supporting it is among the most immature soils on the Moon with a metallic iron abundance of 0.42% and an Is/FeO value of 14−10+6. Additional Landing Camera and Lunar Mineralogical Spectrometer (480–3200 nm) data obtained surrounding the sampling area were used to study the lateral effects of rocket exhaust. All data from soil samples and in situ observations have offered magnetic and spectroscopic constraints on the space weathering state of the Chang'e-5 site. The combined effects of rocket exhaust by removing the top highly weathered soil and the young age of the landing site with lesser degree of impact reworking may attenuate the maturity of Chang'e-5 lunar soils.

Covalent organic frameworks doped with manganese-metal organic framework for peroxymonosulfate activation

A novel N, O modified Mn3O4@porous carbon catalyst (NOC-Mn3O4) was prepared by direct carbonization using the manganese-metal organic framework (Mn-MOF) and covalent organic framework (COF) as precursors to activate peroxymonosulfate (PMS) for the degradation of bisphenol A (BPA) and rhodamine B (RhB). Benefiting from the N and O co-doping of COF, larger specific surface area, faster electron transfer and Mn cycling, the optimum 1NOC-Mn3O4 could significantly improve the degradation performance of BPA and RhB (92.1% and 96.9% within 30 min) as compared to C-Mn3O4 without COF doping. In addition, 1NOC-Mn3O4 showed good reusability and strong anti-interference ability. Radical quenching experiments, X-ray photoelectron spectroscopy (XPS), Electron paramagnetic resonance spectrometer (EPR) and electrochemical tests showed that the 1NOC-Mn3O4/PMS system degraded BPA and RhB by both radical and non-radical pathways. Moreover, the possible degradation pathways of BPA and RhB were proposed by liquid chromatography-mass spectrometry (LC-MS). Except for that, the toxicity of BPA, RhB and their intermediates were evaluated. This study opens up a new prospect for the design of COF-doped PMS catalysts.

Enhancement of microwave fields in pulse EPR of quantum paraelectrics

The pulse electron paramagnetic resonance (EPR) is widely used in different branches of material and life sciences, including promising applications in quantum information processing and quantum sensing. Here, we study the effect of the high polarizability of KTaO3 and SrTiO3 quantum paraelectrics on local electric and magnetic field components of microwaves (MW) at Fe3+ and Mn2+ paramagnetic ions. The measurements are performed with a commercial EPR spectrometer using dielectric and split-ring resonators. It is found that the power of MW pulses used in coherent spin manipulation at nanoseconds timescale decreases to milliwatts as compared to the tens–hundreds of watts usually used for spins in conventional materials. The amplification of MW fields is related to the very high dielectric permittivity (up to 25 000 in SrTiO3) of quantum paraelectrics at GHz frequencies and temperatures below 20 K. This creates the large induced polarization and, thus, huge displacement current and in turn the secondary MW magnetic field. Numerical simulations support the observation of the enhanced magnetic MW field in the high-permittivity sample. The low MW power for excitation of spin transitions in quantum paraelectrics eliminates the requirement of expensive high-power MW equipment. This approach also allows to globally control spin qubits in tandem with integrated devices based on conventional semiconductor MW circuits working at mW powers. It is suggested that quantum paraelectrics can also be used as substrates for deposition of nanoparticles or films of other materials, which would be manipulated by the low-power MW pulses.

Alteration in the molecular structure of the adenine base exposed to gamma irradiation: An ESR study

Abstract Adenine polycrystals were obtained from their powder form under effective crystallization conditions by adjustment of the concentration of chemical solutions. The adenine samples were irradiated with a 60Co gamma-ray source at room temperature for 12, 24, 48, and 72 h, and then these samples were investigated between 240 and 400 K using an electron spin resonance (ESR) spectrometer. No signals were observed in the non-irradiated samples irradiated for 12, 24, and 48 h; however, when irradiated for 72 h, the samples exhibited complex ESR spectra. The analysis indicated the presence of a radical structure, NH ̇ \dot{{NH}} . The hyperfine splitting and g-values were calculated from the spectra by simulation programs. Also, during the measurements, it was observed that the shapes of the ESR lines changed slightly with the temperature.

Highly effective degradation of ibuprofen by alkaline metal-doped copper oxides via peroxymonosulfate activation: Mechanisms, degradation pathway and toxicity assessments

Redox ratios of Cu2+/Cu+ and adsorbed oxygen species (Oads) have shown great activity toward radical generation by activating peroxymonosulfate (PMS). Herein, different alkaline metal oxides (CaO, MgO and BaO) and various amounts of CaO are incorporated into CuO, which could tune the main active sites of redox ratios of Cu2+/Cu+ and Oads. The results show that CaO-CuO-5% exhibits the outstanding performance of PMS activation toward ibuprofen (IBF) degradation with excellent kinetics (k = 0.812 min−1). The X-ray absorption spectroscopy (XAS) and density functional theory (DFT) calculation show that the CaO-CuO-5% has the higher electron density with superior electron transfer ability and lower PMS adsorption energy. Based on radical scavengers and electron paramagnetic resonance spectrometer (EPR), a nonradical process is proposed to play the dominant role. The degradation pathway and the corresponding toxicity of degraded intermediates with residue PMS after reaction is evaluated by LC-MS/MS and bioassay experiments, indicating the lower antagonistic influence on human hormone receptors after advanced oxidation process. Mitigation of the Cu leaching with cyclic stability can be achieved. This study provides a facile method to optimize high-performance catalysts to activate PMS and offer practical environmental applications in the remediation of emerging contaminants.

Ultrasonic assisted activation of persulfate for the treatment of spent porous biochar: Degradation of adsorbed PFOA and adsorbent regeneration

In this work, the regeneration of spent biochar adsorbent and the degradation of adsorbed PFOA by the system of ultrasonic assisted activation of persulfate were explored. The effects of ultrasound, persulfate and biochar on PFOA removal were investigated through a series of regeneration and degradation experiments. Meanwhile, the degradation mechanism and reaction pathways of PFOA were investigated with electron paramagnetic resonance (EPR) and high-resolution quadrupole orbitrap mass spectrometer. The results showed that PFOA adsorbed by biochar could be degraded efficiently with the synergistic effect of ultrasound and persulfate. The degradation of PFOA in biochar could be finished in 4 h, while the defluorination took longer, with a defluorination efficiency of 50.6% after 4 h and 99.6% after 10 h. In this process, PFOA was degraded and defluorinated gradually by thermal decomposition caused by cavitation bubbles and degradation caused by the attack of SO4•ˉ and •OH. Two different free radicals controlled different degradation pathways, with SO4•ˉ playing a dominant role. In this system, the regeneration of the waste biochar adsorbent was achieved by eliminating PFOA, which could be recycled more than three times. The application potential of the system was evaluated using real water sample, and it was found that the removal of PFOA in real water sample was satisfactory even with the influence of inorganic ions and organic matter, indicating that it has promising application prospects. This work provided new insight into the degradation of adsorbed PFOA and adsorbent regeneration.

Insights into a Removal Mechanism of Triclosan Using an Electroactivated Persulfate-Coupled Carbon Membrane System

Triclosan (TCS), a broad-spectrum bacteriostatic agent with bactericidal and disinfectant properties, is one of the emerging pollutants of great interest. The electrically activated persulfate-coupled carbon membrane system was studied in this paper. The removal of triclosan achieved 90% within 40 min. Complete degradation can be achieved within 90 min. The electrode was characterized by scanning electron microscope (SEM) and X-ray photoelectron spectroscopy (XPS). The optimal reaction conditions were explored. The catalytic mechanism of the reaction was investigated. It was proved that hydroxyl radicals, sulfate radicals, and singlet oxygen were the main reactive oxygen species in the reaction process by the free radical quenching experiment and electron paramagnetic resonance spectrometer. The degradation path and mechanism of triclosan were investigated.

Order-of-magnitude SNR improvement for high-field EPR spectrometers via 3D printed quasi-optical sample holders.

Here, we present a rapidly prototyped, cost-efficient, and 3D printed quasi-optical sample holder for improving the signal-to-noise ratio (SNR) in modern, resonator-free, and high-field electron paramagnetic resonance (HFEPR) spectrometers. Such spectrometers typically operate in induction mode: The detected EPR ("cross-polar") signal is polarized orthogonal to the incident ("co-polar") radiation. The sample holder makes use of an adjustable sample positioner that allows for optimizing the sample position to maximize the 240-gigahertz magnetic field B1 and a rooftop mirror that allows for small rotations of the microwave polarization to maximize the cross-polar signal and minimize the co-polar background. When optimally tuned, the sample holder was able to improve co-polar isolation by ≳20 decibels, which is proven beneficial for maximizing the SNR in rapid-scan, pulsed, and continuous-wave EPR experiments. In rapid-scan mode, the improved SNR enabled the recording of entire EPR spectra of a narrow-line radical in millisecond time scales, which, in turn, enabled real-time monitoring of a sample's evolving line shape.

MEPROS – Modular electron paramagnetic resonance operating software for multifunctional high-frequency EPR spectrometer

We present a software solution developed in LabVIEW for a home-built High–Frequency Electron Paramagnetic Resonance (HF-EPR) spectrometer. A modular approach was applied to control the spectrometer subsystems and simplify the adaptation to hardware changes during the development. The solution implements measuring procedures for conventional Continuous Wave EPR (CW-EPR), Frequency–Swept EPR (FS-EPR), and Two-Dimensional EPR (2D-EPR) mapping, which are relevant in different cases. The software’s automation capabilities were tested in several trial measurements to obtain CW-EPR spectra of Silicon Carbide doped by vanadium (SiC + V) at various temperatures and microwave frequencies, multi-frequency spectra via 2D-EPR mapping, and dense FS-EPR data of a lithium phthalocyanine crystal rotated in a magnetic field. Several prospective modifications of the software are discussed in the conclusion. A modular character allows the easy re-use of code portions in other experimental setups. The spectrometer and the software are currently deployed and utilized in a laboratory of EPR spectroscopy at Central European Institute of Technology (CEITEC) in Brno, and data obtained by it has been already used in a number of publications.

The measurement of radiation doses in brachytherapy using an alanine dosimeter

Background: Brachytherapy involves the use of high radiation doses to treat cancer patients, making it essential to have appropriate dosimeter properties to confirm the accuracy and precision of the dose delivered to the patient. Objectives: This study was to investigate the relationship between radiation dose and electron spin resonance (ESR) signal and to evaluate the optimal conditions for the ESR technique. Additionally, the radiation dose from brachytherapy was measured in a solid phantom using alanine in combination with the ESR technique. Materials and methods: The alanine dosimeter (FWT-50-10, Steris, USA), ionization chamber (TW30013, PTW Freiburge, Germany), and transferring tube were positioned inside the solid phantom (Krieger, T9193, PTW Freiburge, Germany), with the BEBIG Co-60 source located at the center of the phantom. Dwell times were calculated to obtain a radiation dose range of 0.06-1.5 Gy. Following irradiation, the alanine derivative was measured using an ESR spectrometer, and a graph was generated to determine the relationship between radiation dose and ESR signal. The uncertainty and fading of the ESR signal were also evaluated. Results: The results indicate that there is a linear relationship (R2 = 0.877) between the radiation dose range of 0.49-1.5 Gy and ESR signal, with a microwave power of 1.5 milliwatt. The uncertainty of the ESR signal was found to be in the range of 0.12% - 3.79%. Signal fading was observed to be in the range of 7.2% - 27.4% over a period of two weeks. Conclusion: Alanine and ESR technique can be used to measure absorbed dose in brachytherapy. The dose response of alanine was linear for radiation doses above 0.49 Gy. The advantages of alanine dosimetry are that alanine is tissue equivalent, nondestructive, small in size, and has low signal uncertainty.

Large cross-effect dynamic nuclear polarisation enhancements with kilowatt inverting chirped pulses at 94 GHz

Dynamic nuclear polarisation (DNP) is a process that transfers electron spin polarisation to nuclei by applying resonant microwave radiation, and has been widely used to improve the sensitivity of nuclear magnetic resonance (NMR). Here we demonstrate new levels of performance for static cross-effect proton DNP using high peak power chirped inversion pulses at 94 GHz to create a strong polarisation gradient across the inhomogeneously broadened line of the mono-radical 4-amino TEMPO. Enhancements of up to 340 are achieved at an average power of a few hundred mW, with fast build-up times (3 s). Experiments are performed using a home-built wideband kW pulsed electron paramagnetic resonance (EPR) spectrometer operating at 94 GHz, integrated with an NMR detection system. Simultaneous DNP and EPR characterisation of other mono-radicals and biradicals, as a function of temperature, leads to additional insights into limiting relaxation mechanisms and give further motivation for the development of wideband pulsed amplifiers for DNP at higher frequencies.