Fluorescence Spectra Research Articles

An X-ray fluorescence experimental method for photon-counting detector in computed tomography system

The X-ray fluorescence (XRF) spectrum of specific elements can be utilized in energy calibration, energy resolution measurement, and analysis of energy response functions for photon-counting detectors (PCDs). The applications can be beneficial for PCD threshold accuracy, performance verification, and optimizing image quality. In previous literature, the experimental configuration for the XRF spectrum typically employed a vertical configuration to avoid the influence of the primary X-ray beam. However, such an experimental configuration is constrained by the fixed position of the X-ray source and detector in the computed tomography (CT) system. Hence, the purpose of this study is to investigate a horizontal configuration for XRF measurements and compare the differences in XRF spectrum with vertical configuration. The results indicate that the spectral characteristics of the horizontal and vertical configurations are similar, suggesting that the horizontal configuration could be applied for energy calibration and spectral analysis in PCD-CT systems.

Constructing stable emulsion gel from gelatin and sodium alginate as pork fat substitute: Emphasis on lipid digestion in vitro

This study aimed to develop a gelatin-sodium alginate (G-SA) emulsion gel that can efficiently hold corn oil, as a substitute for pork fat while controlling the digestive behaviors of lipids in vitro. UV, fluorescence, and circular dichroism spectra and surface hydrophobicity measurements of the G-SA mixtures indicated that gelatin and sodium alginate primarily form aggregates through hydrogen bonds and hydrophobic interactions, and the optimum gelatin-to-sodium alginate w/w ratio was identified as 1.9. The final emulsion gel contained 3.15% gelatin and 1.65% sodium alginate (w/w) with a corn oil content of 40% (w/w). G-SA emulsion gel had a higher proportion of polyunsaturated fatty acids (PUFAs, 53.95 g/100 g) than pork fat (15.17 g/100 g). In addition, the G-SA emulsion gel exhibited stable viscoelastic properties without storage and loss moduli changes at increasing shear rates. The G-SA emulsion gel had a higher melting temperature (42.63 °C) than pork fat (35.07 °C). In vitro digestion studies showed that corn oil had a higher free fatty acid release (40.32%) compared to the G-SA emulsion gel (12.66%) and pork fat (8.53%) (P<0.05), indicating that the digestibility of corn oil was reduced in the G-SA emulsion gel. Calcein release experiments revealed that G-SA emulsion gel released the least amount of calcein (P<0.05) during digestion at a slow rate. The G-SA emulsion gel, similar to pork fat, contained evenly distributed digestive particles encapsulating corn oil after in vitro gastric digestion, with the smallest particle size among the treatments. After the in vitro small intestinal digestion phase, the G-SA emulsion gel maintained small droplet sizes with bridging flocculation. The in vitro digesta of the G-SA emulsion gel contained a significantly higher proportion of PUFAs compared to pork fat (P<0.05). Consequently, the G-SA emulsion gel can be a potential substitute for pork fat, offering higher proportions of PUFAs, lower fat content, and controlled lipid digestion with reduced lipid digestibility.

Photoluminescence and Raman analysis of Nd3+ doped in Ytterbium Zinc Lithium Sodium Barium Calcium Aluminophosphate glasses

Glass of the system:(30-x)P2O5:10ZnO:10Li2O:10Na2O:10BaO:10CaO:10Al2O3: 10Y2O3: x Nd2O3. (where x=1, 1.5,2 mol %) have been prepared by melt-quenching method. (where x=1,1.5 and 2 mol%) have been prepared by melt-quenching technique. The amorphous nature of the prepared glass samples was confirmed by X-ray diffraction. Optical absorption, Excitation, fluorescence and Raman spectra have been recorded at room temperature for all glass samples. Judd-Ofelt intensity parameters Ωλ (λ=2, 4 and 6) are evaluated from the intensities of various absorption bands of optical absorption spectra. Using these intensity parameters various radiative properties like spontaneous emission probability, branching ratio, radiative life time and stimulated emission cross–section of various emission lines have been evaluated

Variations of the elemental composition distribution over the thickness of YBa2Cu3O7-δ thin films obtained by pulsed laser deposition from one target

Epitaxial YBa2Cu3O7‒δ (YBCO) films 150-200 and 300 nm thick, respectively, were deposited on SrTiO3 (100) substrates by pulsed laser deposition at different conditions: with and without using the velocity filtration technique. The films have T(R=0) in the range of 77.4 - 87 R(T) depending on the conditions of deposition from one target with YBa2Cu3O6.8 composition. The films contain Zn, Sr, Pd, Ag and Ti impurity elements obtained from the target (a total of no more than 2 at. % ). Data of the film resistance temperature dependences, X-ray phase analysis, analysis of X-ray fluorescence (XRF) spectra and study of the surface relief by SEM methods revealed the nonuniform distributions of impurity and matrix Y, Ba, Cu elements over the film depth. Impurity concentrations near the surface lead to the formation of faceted spiral pyramids on the surface, which probably evolve into large elongated particles according to the Ostwald mechanism. This knowledge is practically important for optimizing pulsed laser deposition technologies and creating 2D instruments and devices for studying physical phenomena.

Synthesis and characterization of aniline-based azo molecules: In vitro pharmacological and emission studies.

The present work involves the synthesis of novel dispersed mono-azo dyes using different coupling components and 2-methoxy-5-nitro aniline as amine through a simple and convenient diazo-coupling method. The structures of the newly synthesized mono azo dyes were confirmed by using various spectral techniques such as 1H NMR, Fourier transform infrared, and high-resolution mass spectrometry. At room temperature, the electronic absorption spectra and fluorescence spectra of the synthesized mono azo dyes were recorded with different solvents. The global reactive parameters for the synthesized azo molecules were evaluated by performing density functional theory through the 6-311++G (d, p) basis set. The anti-microbial activities for the synthesized azo compounds were carried out, and the compounds G1 and G2 exhibited good antibacterial and anti-fungal activities. The in silico molecular docking studies of the azo molecules revealed that all the compounds exhibited extraordinary binding affinity as that of the standard drug. Further, the anti-tuberculosis study against the Mycobacterium tuberculosis for the synthesized azo dyes was evaluated, and from the results, it was revealed that the compound G4 showed good sensitivity among the other synthesized azo compounds.

Tuning the optical and photophysical characteristics of DR1 through mixing with JGB

A dye mixture of Disperse red1 (DR1) and Janus green B (JGB) was prepared with different concentrations of the two dyes. The optical properties were studied for the two dyes and their mixtures in terms of the absorbance spectra. The direct optical energy gap in addition to the refractive index, extinction coefficient, dielectric constant and optical conductivity were estimated to the two dyes and their mixtures. The experimental energy gap was found to be 2.234 and 1.666 eV for DR1 and JGB respectively, while the values of the energy gaps for the mixtures were found to be ranging between these two values. On the other hand, the refractive index was found to be changed in a systematic way by changing the contents of the dye mixture. The same behavior was also observed for the dielectric constant and optical conductivity. The emission of the two dyes and their mixtures was studied in terms of fluorescence spectra using excitation wavelength of 300 nm where a change in the fluorescence intensity was observed by changing the contents of the mixture. Finally, TD-DFT simulations were performed for the two dyes and their mixture to study the electron density, electrostatic potential, energy gap and optical absorption spectrum and found to be compatible with the experimental measurements.

Hexagonal-inner-cladding fluorotellurite fiber based on hot-extrusion

Laser output power can be significantly enhanced by a double-cladding fiber, as it possesses a large area of inner-cladding for pumping. However, the coupling efficiency of the double-cladding fiber (DCF) is impacted by the shape of the inner cladding. In this study, the simulation results showed that, the hexagonal inner cladding fiber exhibits the highest absorption efficiency of 94.07 % among the fibers with various typical shapes using the three-dimensional ray tracing method at a length of 100 mm. For the experiments, a type of fluorotellurite (TBY, TeO2-BaF2-Y2O3) glass was chosen for its high capacity of rare-earth ions adoption. Subsequently, a finely structured erbium-doped hexagonal DCF was fabricated based on the hot-extrusion method for the first time, with a minimum loss of 1.25 dB/m at 1310 nm. Additionally, the coupling efficiency of the hexagonal DCF was recorded to be 39.47 % at a fiber length of 53 cm, based on the energy distribution experiment. The damage threshold of the hexagonal DCF at 980 nm could be increased to above 26.5 W, nearly doubling that of the single-cladding fiber. Furthermore, a wider fluorescence spectrum with a full width at half maximum (FWHM) of 30 nm was demonstrated by the hexagonal double-cladding fiber, which indicates its potential for high-power laser applications.

Multifaceted Analysis of Bempedoic Acid Binding to Subdomain IIA of Human Serum Albumin

The molecular association between bempedoic acid (BAC) and the major blood plasma transporter, human serum albumin (HSA), was investigated using molecular docking, molecular dynamics (MD) simulation, isothermal titration calorimetry (ITC), atomic force microscopy (AFM), and spectroscopic techniques. During the docking and MD simulation investigations, it was observed that BAC interacted with subdomain IIA (Site I) of HSA through hydrogen bonds and hydrophobic interactions. This interaction ensured the stability of the complex throughout the duration of 100 ns. The observed enhancement in the fluorescence intensity of HSA after BAC inclusion and the swelling of HSA generated by BAC in the AFM data also suggested the formation of a complex between BAC and HSA. The BAC demonstrated a moderate affinity towards HSA, with a binding constant (Ka) of 1.21 ± 0.05 × 105 M−1 at 300 K. Notable modifications in the secondary and tertiary structures of the protein, as well as changes in the protein's Tyr/Trp surroundings, were observed using circular dichroism and three-dimensional fluorescence spectra when the protein was attached to BAC. Insightful information regarding molecular interactions that regulate the stability of the BAC-HSA complex is provided by these investigations.

Exploration of pyridine-thiazolidin-4-one: Synthesis, DFT study, UV–Vis/ fluorescence spectroscopy analysis, antibacterial evaluation and molecular docking

The synthesis of the objective pyridine-thiazolidin-4-one (DCPI-MBT) was involved via the Knoevenagel reaction between 2-((3,5-dichloropyridinyl)imino)thiazolidinone derivative 1 and 4-methylbenzaldehyde 2 over refluxing in acetic acid and sodium acetate. The confirmed structure of this hybrid was elucidated through detailed spectral analyses. A comparison was made between the density functional theory (DFT) configurations of the frontier molecular orbitals in both the gas and solvated ground state (So) and the solvated excited state (S1). UV–Visible and fluorescence spectra of the thiazolidin-4-one derivative were obtained in DMSO, displaying a significant Stokes’ shift (Δν¯= 3136.81 cm−1). The synthesized DCPI-MBT was established to see how well they killed different kinds of pathogenic microbes, such as bacteria, viruses, and fungi. These results demonstrate that the synthesized DCPI-MBT has a broad-spectrum antibacterial capability that is on par with or even superior to conventional treatments in certain instances. Moreover, molecular docking simulation was used to evaluate the bindings of the synthesized DCPI-MBT with a target protein (PDB: 1kzn). The binding energies, RMSD values, kinds of interactions with amino acid residues, and interaction distances of the hybrids were determined based on their substituent changes. This study analyzed the pharmacokinetic profiles of newly DCPI-MBT, using SwissADME predictions to focus on their potential as therapeutic agents. The DCPI-MBT has the promising pharmacokinetic profile for future development as a therapeutic drug, with optimum solubility, bioavailability, and a favorable interaction profile with biological targets.

Spectrofluorimetric Method for Simultaneous Determination of Trimethoprim and Sulfamethoxazole with &lt;i&gt;O&lt;/i&gt;-phthaladehyde Reagent by H-point Standard Addition Method

Simultaneous spectrofluorometric method described for the determination of trimethoprim (TMP) and sulfamethoxazole (SMZ) in pure and pharmaceutical preparations using H-point standard addition method (HPSAM) according to the reaction of nanograms of drugs with O-phthaladehyde (OPA) reagent to forms highly fluorescence compounds. The formed fluorophore excitation and emission at 342 and 458 nm, respectively, for OPA-TMP compound, at 424 and 508 nm, respectively, for OPA-SMZ compound under basic condition (pH 9.8) in the presence of 2-mercabtoethanol. A simple and accurate HPSAM is reported to resolve the overlapping in the fluorescence spectrum of these two drugs without prior separation of samples. The linear range was 100–1200 ng/mL for TMP and 100–1100 ng/mL for SMZ. The LOD and LOQ were 16.64 and 36.80 ng/mL, as well as 15.76 and 33.88 ng/mL for TMP and SMZ, respectively. The relative standard deviations and recovery percentages were 0.641% and 101.29% for TMP as well as 0.558% and 100.96% for SMZ, respectively. The procedure has been applied successfully in various pharmaceutical preparations. It was discovered that the experimental F- and t-values at a 95% confidence level were no higher than the theoretical values, showing that the HPSAM method is accurate and valid.

A Fluorescent Probe for Hydrazine Based on 4-hydroxycoumarin with High Selectivity and Sensitivity

Background: Therefore, the development of reliable analytical techniques with high selectivity and sensitivity to detect hydrazine is required for the protection of human health and safety. Objectives: Traditional methods for detecting N2H4 are frequently time-consuming, less accurate, and unsuitable for the analysis of living systems. Numerous fluorescent probes for hydrazine have been produced and gained some valuable results recently. The creation of a simple fluorescent probe for hydrazine detection is the goal of this project Method: In this study, 300 µL of probe 3-methyl-2-oxo-2H-chromen-7-yl propionate (MOCP) was mixed with an equivalent amount of the solution of each analyte to obtain the measurement solution. Following a 10-minute room temperature incubation period, the fluorescence spectra of the resultant solution were recorded. Results: The fluorescence intensity of the probe was noticeably enhanced when N2H4 was added to the probe, but almost no fluorescence enhancement was observed when other competitive ions were added. Conclusion: A hydrazine fluorescent probe based on 4-hydroxycoumarin fluorophore was developed. The probe MOCP displayed high sensitivity and selectivity for hydrazine, with a color change from colourless to blue for detection by the naked eye. Moreover, it demonstrated a low detection limit of 20 nM and a fast reaction time of 30 s.

Continuous Wavelet Transform as a Signal Processing Technique for Spectrofluorimetric Analysis of Rosuvastatin and Losartan: Greenness and Blueness Assessment.

In this study, the application of continuous wavelet transform as a signal processing technique for the spectrofluorimetric determination of rosuvastatin and losartan is investigated. Both rosuvastatin and losartan exhibited native spectrofluorometric signals with severe overlapping peaks, making their simultaneous determination challenging. To address this issue, rbio 2.4 wavelet transformation was employed to obtain zero-crossing points in the synchronous fluorescence spectra of losartan and rosuvastatin at 346 and 408 nm, respectively, making their quantification possible. The developed method was validated according to the ICH guidelines and displayed high accuracy, precision, and specificity. The method exhibited excellent linearity over concentration ranges 0.2-2.0 and 0.25-2.0 μg/mL for losartan and rosuvastatin, respectively. In addition, LOD and LOQ were 0.046 and 0.140 μg/mL for losartan and 0.036 and 0.110 μg/mL for rosuvastatin, respectively, indicating the high sensitivity of the developed method. Moreover, greenness and blueness assessments were carried, revealing a high AGREE score of 0.71 and BAGI score of 77.5 for the developed method, making it a promising greener alternative for the reported chromatographic methods. Finally, the developed method was applied to the determination of rosuvastatin and losartan in pharmaceutical formulations, posing it as a powerful greener alternative in quality control laboratories.

Effect of AlF3 and KF addition on the structure and luminescent properties of P2O5 – K2O – Nb2O5 – Bi2O3 glasses doped with Eu3+

Based on the developed phosphate glasses P2O5–K2O–Bi2O3–Nb2O5 doped with Eu3+, the influence of AlF3 and KF on the structural and luminescent properties was investigated. For this purpose, three series of glasses containing from 5 to 15 mol% fluorides were synthesized. Two of the series included the KF additive, which was introduced in two ways - proportionally and disproportionately at the expense of the K2O share. The structural characterization (XRD, FTIR) allowed us to determine the evolution of the internal structure of the glasses caused by changes in the type and content of the introduced additives and the presence of the Eu dopant. Similarly, using DSC/DTA, the thermal properties of undoped matrices were defined. The luminescence enhancement caused by the addition of ≥10 mol% fluorides was confirmed by the obtained fluorescence spectra. The presented studies not only expand the state of knowledge about the effects of fluorides on phosphate glasses but also demonstrate the ease of obtaining materials with improved properties suitable for use as phosphor in LEDs.

Low-temperature treatment optimization for diesel-contaminated kaolin: Mutual impacts of generated pyrolytic carbon and particle agglomeration

Efficiency improvement in low-temperature treatment for diesel-contaminated sites is urgent because changes in soil properties and the generation of new substance during the remediation process can influence the duration and energy utilization. This paper focuses on low-temperature treatment optimization based on the mutual impacts of pyrolytic carbon and kaolin aggregation. Results reveal that the peak mass loss rate occurred between 100–150°C, with minimal loss beyond 200°C. Samples thermally treated at 150–200°C exhibited darker colors, indicating pyrolytic carbon formation, corroborated by x-ray photoelectron spectroscopy (XPS), fourier transform infrared spectroscopy (FTIR), and three-dimensional fluorescence spectrum (3D-EEM) analyses. Additionally, diesel contamination influenced the fractal dimension of aggregates by influencing adhesion forces (<10000 mg/kg) and forming liquid bridges (≥10000 mg/kg) in untreated kaolin, resulting in an initial increase and subsequent fall in fractal dimension with increasing concentration. Decline rates of pollutant gas concentration were closely correlated with fractal dimension changes under thermal conditions due to pollutant volatilization and pyrolytic carbon formation. Based on the consistency between fractal dimension and decline rate, two critical remediation concentrations (C0) and temperatures (T0) indices were identified to optimize the low-temperature remediation.

Probing mechanism of Rhodamine B decolorization under homogeneous conditions via pH-controlled photocatalysis with anionic porphyrin

Porphyrins are acknowledged for their efficacy as photosensitizers and show potential for the treatment of water contaminated with diverse dyes. This research emphasizes the use of meso-tetra(4-sulfonatophenyl)porphyrin (TPPS) as a photosensitizer for purifying water contaminated with rhodamine B. Investigations were conducted under homogeneous conditions using visible light irradiation, revealing the efficacy of the porphyrin in the decolorization of rhodamine B strongly depends on pH of the solution. This study demonstrated that within 120 min, the decolorization process rapidly removed about 95% of RhB at an initial pH of 3.0, while at pH 6.0, the removal rate was significantly lower, at only 12%. An extensive photophysical study of the TPPS was carried out at pH 6.0 and pH 3.0 including absorption and fluorescence spectra, fluorescence quantum yields, triplet absorption spectra, triplet lifetimes, triplet and singlet oxygen quantum yields in order to explain difference in the efficiency of RhB discoloration. A thorough investigation into mechanism revealed that neither reactive oxygen species nor singlet oxygen played a role in RhB decolorization within this system. Instead, the predominant route was found to be the electron transfer from photoexcited TPPS to RhB, followed by proton transfer at pH 3.0, leading to the generation of a colorless leuco form.

A terphenyl derivative-based colorimetric-fluorimetric probe for the detection of lysine and arginine and their bioimaging

Lysine (Lys) and arginine (Arg) play a crucial role in the human diets, medical diagnostics, and functional biomaterial synthesis. The imbalance of intake for these two amino acids causes various diseases. Although many analytical techniques have been reported for the detection of amino acids, there are still some issues such as the need for bulky instruments, professional operators, sensitivity to be improved, and real-time detection. Here, a novel colorimetric-fluorimetric probe based on a terphenyl derivative (TPT) has been synthesized for the precise detection of Lys and Arg. In the EtOH-H2O solution of TPT, the NH2 group at the chain end of Lys/Arg undergoes a nucleophilic addition reaction with CN groups of benzothiazole groups of the probe TPT, which breaks the initial long-conjugated system of the probe molecule. As a result, blue shifts can be observed for both UV–vis absorption spectra and fluorescence spectra, accompanying with color changes of the TPT solution. The UV–vis absorption peak of TPT solution shifts from ∼410 nm to ∼325 nm, and the solution color changes from light-yellow to colorless. The fluorescence emission shifts from ∼580 nm to ∼470 nm and the bright-yellow TPT solution changes to blue under the irradiation of 365 nm UV light. For colorimetric method, the limits of detection (LoD) are 0.82 μM and 0.90 μM for Lys and Arg, respectively. For fluorimetric method, they are 2.02 nM and 1.62 nM for Lys and Arg, respectively. In addition, TPT has good selectivity and anti-interference for Lys and Arg. The synthesized probe TPT has been successfully used for the precise detection of Lys and Arg in drugs and for fluorescence imaging of living cells. This work demonstrates that terphenyl-based derivatives are promising organic probes for the detection of Lys and Arg, providing a new way for designing other amino acids probes.

Synthesis of Ferrocenyl Chalcone-Containing Aminourea Schiff Bases and Their Detection on Tryptophan.

In this paper, 1-phenyl-3-ferrocenylenone aminourea Schiff bases were synthesized by a novel method. A multifunctional molecular probe (Probe A) of 1-phenyl-3-ferrocenylenone, carbon-based solid acid, aminourea, and anhydrous ethanol was synthesized by adding them to a vessel at elevated temperatures and refluxing for the synthesis of a multifunctional molecular probe (Probe A) of 1-phenyl-3-ferrocenylenone aminourea Schiff base, and it was found that it recognizes tryptophan (Trp) in solution, and that the catalyst can be reused more than five times after recycling. This method is characterised by low cost, high efficiency, green environment and no waste acid. Fluorescence and UV spectra show that probe A specifically recognizes tryptophan (Trp) without interference by other amino acids or pH and time does not affect it within 45min. The lowest limit of detection for Trp was 1.307 × 10- 4 mol/L for probe A. The binding ratios of probe A to Trp were measured to be 1:1 by Job's plotting method, respectively. The complexation constant of probe A with Trp was found to be 2.733 × 107 L/mol according to the Benesi-Hildebrand equation. The bonding mechanism was explored through IR spectroscopy and ¹H NMR titration.

Understanding the Hydrocarbon Accumulation Process in Deep–ultradeep Oil and Gas Reservoirs in Complex Structural Areas—The Qixia Formation in the Shuangyushi Structure in Northwestern Sichuan Basin, China

Deep-ultradeep oil and gas reservoirs in complex structural areas have typically undergone multistage tectonic processes that have a considerable influence on the hydrocarbon composition, isotopic composition, and other geochemical characteristics of petroleum. By assessing the charging period of hydrocarbon accumulation during a particular age we can determin these changes. We studied the characteristics of fluid inclusions developed in the dolomite reservoir in the Middle Permian Qixia Formation in the Shuangyushi structure of the northwestern Sichuan Basin using methods such as inclusion petrography, microbeam fluorescence fluorescence spectroscopy, and inclusion homogenization temperature. Furthermore, the main peak wavelength of the fluorescence spectrum, red–green ratio/chromatic parameter, Q650/500, as well as the chromatic parameter corresponding to emission flux at 535 nm (QF535) and their correlations with the homogenization temperature distribution, were used to identify the charging period of hydrocarbons in the Qixia Formation. The results show that different types of fluid inclusions were developed in the Qixia Formation. The fluorescence of hydrocarbon inclusions is mainly blue, with a small amount of yellow–green and orange–yellow. The max of orange–yellow, yellow–green, and blue fluorescence of the hydrocarbon inclusions range between 562 ∼ 579 nm, 497 ∼ 548 nm, and 447 ∼ 497 nm, respectively. The distribution of the homogenization temperatures during the same period ranges from 100 °C to 110 °C, from 120 °C to 140 °C, and from 160 °C to 170 °C, respectively. By combining the burial and thermal evolution histories of the Qixia Formation, we concluded that the Qixia Formation has experienced three stages of oil and gas charging, with the time of 204, 185 and 158 Ma. This method is of great significance to determine the date and duration of oil and gas accumulation, and provides technical support for the recovery of ultra-deep hydrocarbon accumulations in complex structural areas.

Optimization of GEM detectors for applications in X-ray fluorescence imaging

In this work a set of simulations that aim at the optimization of Micropattern Gaseous Detectors (MPGD) for applications in X-ray fluorescence imaging in the energy range of 3–30keV is presented. By studying the statistical distribution of electrons from interactions of X-rays with gases, the energy resolution limits after charge multiplication for 6keV X-ray photons in Ar/CO2(70/30) and Kr/CO2(90/10) were calculated, resulting in energy resolutions of 15.4(4)% and 14.6(2)% respectively. These two mixtures were studied in simulations to evaluate the advantages of using krypton-based mixtures to reduce the presence of escape peaks in fluorescence spectra. A model to evaluate the X-ray fluorescence from the conductive materials inside the detectors was implemented, serving as a tool to estimate the extent of contamination of fluorescence spectra when using copper or aluminum layers in the material composition of MPGDs.

A new approach to assessing the consequences of radiation on the eye

The authors propose a new approach to assessing the consequences of exposure to ionizing radiation on the structures of the eye. The approach is based on the results recently obtained by the authors together with employees of the Joint Institute for Nuclear Research in Dubna, according to which radiation exposure causes oxidation of the bisretinoids contained in the structures of the eye - the retina and retinal pigment epithelium. As a result of this oxidation, the fluorescence spectrum of bisretinoids shifts to the blue region of the visible spectrum. The shift in the fluorescence spectrum can be recorded non-invasively using the method of recording fundus autofluorescence, which is currently generally accepted in ophthalmology. Since the oxidation of bisretinoids occurs during radiation exposure, it becomes possible almost immediately after irradiation to assess the degree of impact of ionizing radiation on both the structures of the eye and the body as a whole. There is no analogue to such a non-invasive assessment of the effects of radiation on the body. The proposed approach may become important for assessing the radiation safety of nuclear industry workers, astronauts, and patients undergoing proton or gamma therapy.