Luminescence Analysis Research Articles

Regionally extensive ejecta layer of the Australasian tektite strewn field: the MIS 20/19 large meteorite impact in mainland South-East Asia

Aspects of the Quaternary sedimentary geology of South-East Asia have proven problematic in terms of interpretation as to the origins and relationships of the surface sediment layers. The MIS 20 large meteorite impact (c., 788 to 785 ka) occurred within mainland South-East Asia, evident from the well-researched ‘Australasian Tektite Strewn Field’ which extends over at least one tenth of the surface of the Earth. Key questions include: 1) whether the sedimentary impact signature is preserved in the Quaternary sediment cover of the region and 2) whether stratigraphic indicators and dating methods can discriminate meteorite impact-related associations of sedimentary strata, despite subsequent reworking and diagenesis. The importance of the questions raised relate to the search for the impact site, which has not been located conclusively. Moreover, the sedimentary signatures of meteorite impacts are not well known and the descriptions in this study should aid the recognition of impact signatures elsewhere in the world. An hypothesis was developed: Surface Quaternary sediments across a wide area of mainland South-East Asia represent the effects of a regionally significant meteorite impact. Over one hundred sedimentary sections were logged across five countries in mainland South-East Asia. Methods used, defining the stratigraphy and sedimentology, include computed tomography and X-ray scanning, geochemistry, magnetic susceptibility, and environmental luminescence as well as conventional grain size analyses. Luminescence analyses were applied to samples from key strata to provide age constraints and indications of reworking through dose distributional analysis of quartz fractions. The results of the investigation explain the nature of the stratigraphy and relate it specifically to the meteorite impact. In this manner, the strata and sedimentary signatures of the ejecta from a large cosmic impact are defined across a broad region, rather than being described at singular and isolated sections. The novelty is the spatial scale of the investigation which nevertheless remains detailed. A summary model of impact stratigraphy is presented that applies to the regional ejecta blanket covering at least 300,000 km2. Tektites were co-deposited with the ejecta and not introduced by surface processes reworking the deposits. Similar models may be applicable outside of mainland South-East Asia, wherever other large impacts are suspected to have occurred.

Thermoluminescence characteristics of BeO doped with Si, Mg, and Cr: Density functional theory calculations and One trap – One recombination center model simulations

The incorporation of first principles computational methods in Thermoluminescence (TL) enables the comprehensive investigation of the luminescent characteristics exhibited by solid materials. These calculations offer valuable insights into the electronic structures and thermal behavior, providing a deeper understanding of the underlying mechanisms. Density Functional Theory (DFT) is a powerful tool for predicting the electronic structure properties, as the Density of States (DOS) of materials. By theoretically depicting the electronic states arising from electron transitions, the present study focuses on the DFT study of undoped BeO and of BeO with substitutional Si4+,Mg2+ and Cr3+,Mg2+ doping, and the connection of TL emission caused by recombination of electrons in centers, as outlined in the One Trap – One Recombination (OTOR) center model. This approach offers essential details regarding the origins of electron traps, facilitating a deeper exploration of the intrinsic contribution of DFT in Stimulated Luminescence (SL) analysis.

Unlocking Single-Particle Multiparametric Sensing: Decoupling Temperature and Viscosity Readouts through Upconverting Polarized Spectroscopy.

Upconverting particles (UCPs), renowned for their capability to convert infrared to visible light, serve as invaluable imaging probes. Furthermore, their responsiveness to diverse external stimuli holds promise for leveraging UCPs as remote multiparametric sensors, capable of characterizing medium properties in a single assessment. However, the utility of UCPs in multiparametric sensing is impeded by crosstalk, wherein distinct external stimuli induce identical alterations in UCP luminescence, hindering accurate interpretation, and yielding erroneous outputs. Overcoming crosstalk requires alternative strategies in upconverting luminescence analysis. In this study, it is shown how a single spinning NaYF4:Er3+, Yb3+ upconverting particle enables simultaneous and independent readings of temperature and viscosity. This is achieved by decoupling thermal and rehological measurements-employing the luminescence of thermally-coupled energy levels of Er3+ ions for thermal sensing, while leveraging the polarization of luminescence from non-thermally coupled levels of Er3+ ions to determine viscosity. Through simple proof-of-concept experiments, the study validates the capability of a single spinning UCP to perform unbiased, simultaneous temperature, and viscosity sensing, thereby opening new avenues for advanced sensing in microenvironments.

Er3+ -doped oxyfluoroborosilicate glass ceramics with embedded CaF2 nanoparticles for 1.53 μm broad band applications

The CaF2 based oxyfluoroborosilicate glasses and glass ceramics doped with Er3+ ions were prepared via melt quench process followed by heat treatment and characterized for 1.53 μm broadband applications. The optimized glass ceramic sample was obtained at 450oC/1h heat treatment. The Er3+ concentration was optimized as 1.0 mol% for efficient emission at 460 nm excitation through concentration dependent luminescence analysis. The spectroscopic parameters such as Ωλ = 2,4,6 parameters and the radiative parameters such as spontaneous transition probability rates (AR), branching ratios (βR) and decay times (τR) were calculated applying the standard Judd-Ofelt theory. The effective bandwidth (Δλeff), stimulated emission cross-section (σe), gain bandwidth (σe × Δλeff), quantum efficiency (η) and figure of merit (σe × τR) were calculated as 25.78 nm, 13.42 × 10−21 cm2, 3.46 × 10−26 cm3, 82.83% and 5.32 × 10−23 cm2s, respectively for the optimized glass ceramic sample. The exchange type of energy transfer among the excited Er3+ ions results the quenching in luminescence and the non-exponentiality in decay curves. The systematic investigations carried out indicate that the glass ceramic obtained at 450oC/1h heat treatment was proficient for 1.53 μm broadband fiber lasers and optical amplifiers in S and C band communication window.

Improving the Stability, Water Solubility, and Antioxidant Activity of α-Tocopherol by Encapsulating It into Niosomes Modified with Cationic Carbamate-Containing Surfactants.

The low solubility of α-tocopherol in water and its susceptibility to photodegradation make it difficult for biological systems to absorb this natural antioxidant. To overcome these limitations, α-tocopherol was encapsulated in low-toxicity nanocontainers, namely, niosomes based on Tween 80 and cholesterol. The niosomes were modified with cationic surfactants containing a carbamate fragment. The size and charge of the particles were determined and their stability was assessed using dynamic and electrophoretic light scattering methods. It was found that the introduction of cationic surfactants to niosome formulations significantly improved their physicochemical properties and increased stability due to a positive charge of up to +40 mV being generated. Modified niosomes loaded with α-tocopherol were characterized by a hydrodynamic diameter of 100-120 nm, a narrow particle size distribution, and a high encapsulation efficiency of more than 90%. Testing the photochemical stability of α-tocopherol using a spectrophotometric method demonstrated that niosomes were able to protect this substance from UV irradiation. Luminescence analysis showed that the inclusion of α-tocopherol in niosomes increased their antioxidant activity by 30%. An acute toxicity study has demonstrated the safety of the systems. The LD50 value for niosomes modified with carbamate-containing surfactants and loaded with α-tocopherol exceeded 10,000 mg·kg-1 (mice, intraperitoneal and oral administration).

Improving storage duration of tomatoes (Solanum lycopersicum) through electron beam technology.

Electron beam (EB) technology typically consists of high-energy electron streams produced by a linear accelerator. Although promising, the use of EB irradiation as a technique to delay ripening and prevent spoilage in tomatoes has not been extensively investigated. In this study, the effectiveness of EB irradiation in prolonging the shelf life of tomatoes postharvest was investigated. The results indicated that EB irradiation successfully reduced microbial contamination and decay, preserved key quality attributes (such as total soluble solids, titratable acidity, pH, and firmness), and significantly minimized weight loss. Notably, the treatment delayed the biosynthesis of lycopene, a key indicator of ripening, without adversely affecting phenolic content and antioxidant activity, which remained consistent regardless of irradiation. Additionally, different methods for detecting irradiation were evaluated. Thermoluminescence analysis proved to be the most dependable technique, especially for doses exceeding 600Gy, due to its high sensitivity and specificity. In contrast, photostimulated luminescence and electron spin resonance analyses showed limitations in accurately identifying the irradiation status of foods with high moisture content, such as tomatoes. This study confirms that EB irradiation, while maintaining postharvest quality, extends the shelf life of tomatoes by 5-10days, suggesting its potential for commercial application in food preservation.

Luminescence, temperature sensing and Judd-Ofelt analysis of Bi2Mo3O12:Eu3+ phosphors and the application in latent fingerprint visualization

Eu3+-activated materials have garnered significant attention due to their outstanding optical characteristics. In this work, the sol–gel method was successfully used to prepare Bi2Mo3O12 phosphors doped with different amounts of Eu3+. The generated samples were identified as orthorhombic Bi2Mo3O12 with a scheelite-like structure by X-ray diffraction analysis of the crystal structure. The sample’s morphology and size were examined using scanning electron microscopy and transmmission electron microscopy, which revealed irregular block morphology and tens to hundreds nanometers scale dimension. From the analysis of the concentration-dependent luminescence intensity of Eu3+, it was confirmed that the exchange interaction was responsible for the quenching of 5D0 fluorescence of Eu3+. When excited at 374 nm, the phosphor emitted brilliant red light, with the highest emission occurring at 616 nm (5D0→7F2 transition), and the calculated color coordinates of the sample were (0.663, 0.336). By examining the temperature dependence of the emission spectra, the temperature sensing performance of the sample and the thermal quenching behavior of Eu3+ luminescence was explored. Furthermore, the optical transition property of Eu3+ was investigated by using the emission spectra and fluorescence lifetime within the context of Judd-Ofelt theory. Ultimately, latent fingerprint visualization of the sample on various object surfaces was studied, thanks to the intense luminescence and small particle size of the Bi2Mo3O12:Eu3+ phosphor. The results indicated that the sample can clearly display the different hierarchical features of fingerprint on different object surfaces.

Downstream change of luminescence sensitivity in sedimentary quartz and the rearrangement of optically stimulated luminescence (OSL) components along two large rivers

Recently, it has been proposed that the luminescence sensitivity of quartz grains, i.e. their luminescence response to unit dose, might be used for sediment fingerprinting. Sensitivity is determined both by the origin of quartz grains and the sedimentary processes they underwent. However, a more detailed understanding of the factors influencing sensitivity is essential in order to expand and specify the applicability of the parameter in sediment sourcing and geomorphological studies alike. In the present research, we examined the spatial changes of sensitivity parameters of coarse grain quartz in modern sediments of the largest rivers of the Carpathian Basin, Central Europe, to determine the role of source areas and transportation distance.Based on the luminescence analysis of 39 samples, quartz extracts with a Carpathian origin (catchment of the Tisza River have a significantly higher sensitivity, except the LM-OSL medium component, than those originating from the Alpine domain (catchment of the Danube River). No clear relationship could be identified between natural sensitisation and transportation distance. In terms of the Tisza the observed downstream increase of quartz sensitivity is due to high sensitivity quartz grains supplied by its tributaries. In the meantime, a recurring change was observed along the Danube, which can be attributed mostly to local erosional processes. Consequently, tributaries and erosion can overprint the potential downstream sensitisation of quartz grains in large rivers.Meanwhile, in terms of the Danube on sections where a significant downstream increase was detected in LM-OSL fast component sensitivity, LM-OSL medium component sensitivity systematically decreased. Additionally, during laboratory sensitization, the CW-OSL sensitivity of Danube samples increased considerably, whereas changes were more moderate in the case of Tisza samples. Moreover, in the case of Tisza-related quartz extracts, the 110°C TL sensitivity and the LM-OSL fast and medium components showed a strong correlation, indicating the stability of luminescence processes (trapping and recombination). Whereas, in the case of the Danube both LM-OSL components show a weak correlation with the 110°C TL intensity. All these indicate that Alpine-origin quartz grains are more susceptible to the rearrangement of electron traps and/or recombination centres, which can also be an indicator of sediment sources in Quaternary studies in the region.

Remnant of the Late Holocene sand beach reveals ancient settlement-related sea level change from western Thailand

Archaeological findings and analysis of the sand beach at the Ban Khu Bua site in western Thailand indicate substantial sea-level shifts, which relate to sea-level regression during the late Holocene. This research focused on analyzing the paleo-shoreline and determining the age of ancient sandy beach deposits. Satellite imagery (Sentinel-2A) taken in 2021 facilitated classification of the paleo-coastal landforms into four main categories: colluvium, recent floodplain, old tidal flat, and old sandy beach. The latter, running predominantly north to south, is composed of fine to very fine sand characterized by sub-angular to round shapes, high sphericity, and well sorted. The sediment’s mineral composition is primarily quartz, accompanied by smaller rock fragments, organic matter, heavy minerals, and feldspars. Optically Stimulated Luminescence analysis of quartz-rich samples from the inner and outer areas suggested deposition of the old sandy beach sediments between 1,500 and 3,000 years ago in the inner part, pre-dating the establishment of the Khu Bua community in the Dvaravati period. Continuous beach sand deposition along Thao U-Thong Road aligns with the community settlement approximately 200 to 1,000 years ago.

Optical Characteristics of a New Molecular Complex: "Nafion-Colloidal CdSe/CdS/ZnS Nanocrystals".

Here, the optical properties of the Nafion polymer membrane containing colloidal CdSe/CdS/ZnS nanocrystals embedded by diffusion have been studied. The CdSe/CdS/ZnS nanocrystals have a core/shell/shell appearance. All experiments were carried out at room temperature (22 ± 2) °C. A toluene solution was used to provide mobility to the active sulfone groups of the Nafion membrane and to embed the nanocrystals inside the membrane. The diffusion process of colloidal CdSe/CdS/ZnS nanocrystals into Nafion proton exchange membrane has resulted in a new molecular complex "Nafion-colloidal CdSe/CdS/ZnS nanocrystals". The kinetics of the nanocrystals embedding into the membrane matrix was investigated using luminescence analysis and absorption spectroscopy techniques. The embedding rate of CdSe/CdS/ZnS nanocrystals into the Nafion polymer membrane was approximately 4·10-3 min-1. The presence of new luminescence centers in the membrane was proved independently by laser emission spectroscopy. The luminescence spectrum of the resulting molecular complex contains intensity maxima at wavelengths of 538, 588, 643 and 700 nm. The additional luminescence maximum observed at the 643 nm wavelength was not recorded in the original membrane, solvent or in the spectrum of the semiconductor nanoparticles. The luminescence maximum of the colloidal CdSe/CdS/ZnS nanocrystals was registered at a wavelength of 634 nm. The intensity of the luminescence spectrum of the membrane with embedded nanocrystals was found to be higher than the intensity of the secondary emission peak of the initial nanocrystals, which is important for the practical use of the "Nafion-colloidal nanocrystals" complex in optical systems. The lines contained in the luminescence spectrum of the membrane, which has been in solution with colloidal nanocrystals for a long time, registered upon its drying, show the kinetics of the formation of the molecular complex "Nafion membrane-nanocrystals". Colloidal nanocrystals located in the Nafion matrix represent an analog of a luminescent transducer.

Silver sulfide quantum dots stabilized with l-Cysteine - Optimization of synthesis in aqueous phase and optical characterization

In this study, we investigate the properties of silver sulfide (Ag₂S) quantum dots (QDs) coated with l-cysteine (L-Cys). We elucidate the formation mechanism of Ag₂S/L-Cys QDs from AgNO₃, Na₂S, and L-Cys through FT-IR, TEM and luminescent analyses. The influence of reaction parameters on the spectroscopic properties, including absorption spectra, emission spectra, fluorescence lifetime, and quantum yield, is thoroughly examined. We propose an optimal fabrication processing by analyzing the properties of QDs throughout the reaction process. Additionally, we demonstrate that 4–6 nm Ag₂S QDs can be effectively imaged using high resolution transmission electron microscopy (HR-TEM) which is particularly beneficial for developing layers incorporating these nanoparticles. Our findings are systematically compared with previous literature, providing a comprehensive understanding of the properties and potential applications of L-Cys coated Ag₂S QDs.

Continuous ion beam-induced luminescence (IBIL) spectroscopy of air-borne particulate matter hourly collected from the atmosphere

We investigated the applicability of Ion Beam Induced Luminescence (IBIL) analysis for identifying biological components in sequentially collected airborne particulate matter (PM) samples obtained using the automated sampler. A series of micro-IBIL spectroscopies were performed on a PTFE (polytetrafluoroethylene) membrane tape filter from the Atmospheric Environmental Regional Observation System (AEROS) during a highly concentrated air pollution event on 26–27 March 2020, collected at Ota, Japan (36.290°n, 139.381°e) using an external 3 MeV proton microprobe. IBIL at typical wavelengths associated with organic compounds such as NADH and riboflavin were identified through the series of IBIL analyses, which is a key factor for identifying existence of organic pollutions, or bioaerosols. The decay times of the IBIL indicate that the peak measured is due to organic compounds rather than inorganic particles or ambient substances. These results suggest that micro-IBIL spectroscopy can be used to identify bioaerosols in hourly collected AEROS PTFE membrane tape filters taken from the atmosphere.

Multi-excitation photoluminescence spectroscopy system for gemstone analysis.

Luminescence spectra can reveal important chemical and structural information that can be used for gemstone characterization and identification. Traditionally, gemstone UV-excited luminescence is evaluated visually under mercury vapor lamp illumination. This approach is limited by several factors, including the mixture of mercury's emission peaks, possible filter degradation, an inability to separate overlapping emission features, and the sensitivity and subjectivity of human vision and color interpretation. A multi-excitation photoluminescence (PL) spectroscopy system has been built for gemstone analysis, incorporating 261 and 405nm laser excitations to study gemstone emission features between 270 to 1000nm. This system presents significant improvements, extending the detection spectral range, increasing the sensitivity, accuracy and reproducibility of gemstone luminescence analysis. Luminescence analysis of commercially valuable gemstones are presented to demonstrate the system's suitability for gemstone identification. Examples include distinguishing natural from laboratory-grown diamonds, thermal and color treatment detection for corundum and pearls, respectively, and mineral type separation of emeralds and other green gemstones.

Mechanism and dynamic analysis of persistent luminescence in phosphors Sr2MgSi2O7: Eu2+, Dy3+

The persistent luminescent (PSL) phosphors Sr2-x-yMgSi2O7: xEu2+, yDy3+ (x = 0∼0.08, y = 0∼0.08) were synthesized by a solid-state reaction method in a weak reductive atmosphere of 5%-H2/N2. Comprehensive measurements were carried out to study the effects of Eu2+ and Dy3+ doping amount on the crystal phase, photoluminescence (PL), afterglow decay properties, and trap energy levels. The results indicated that the impurity phases decreased and disappeared, and crystalline grains tended to be larger and denser with the doping amount of Eu2+ and Dy3+ increasing. We shed light on the origination of asymmetric PL peak, concentration quenching of Eu2+ ions, time evolution of PSL specture and chromaticity of Eu2+, Dy3+ co-doped phosphors. Based on the deconvolutions of X-ray photoelectron spectroscopy (XPS) spectra and thermoluminescence (TL) spectra, the types and energy depth of traps in these phosphors were systematically studied. According to the data of PL, PLE, and TL, we deduced a schematic diagram of the energy level and discussed the mechanism of PSL of the phosphors. As Dy3+ dopant increases, the Eu2+, Dy3+ co-doped phosphors not only generate more defects of VO•• and VSrʺ, but also introduce DySr• defect with proper trap depth, meanwhile, a thermally assisted tunneling mechanism will gradually dominate during the persistent luminescence, which is responsible for that the phosphor with x = 0.02, y = 0.01 presents the best long afterglow property.

Synthesis of eco-friendly borosilicate glass with Eu3+ dopants: Harnessing recovered silica gel waste for reddish-orange emission materials

In this study, recovered silica gel waste (RSGW) is used as a key raw material to create borosilicate glass doped with Eu3+ ions in a new and environmentally friendly way. The glass compositions were fabricated using the melt quenching method, with different amounts of RSGW and a constant 1.0 mol% Eu3+ doping concentration. The study shows that increasing the doping concentration of RSGW improves the glass density and rigidity while reducing the molar volume, indicating enhanced glass stability. Photoluminescence and X-ray luminescence analyses confirm that the optimal composition with 50 mol% RSGW exhibits the strongest emission. Based on the phonon sideband analysis, the host glasses have a phonon energy of 966.53 cm− 1. An X-ray absorption near-edge structure (XANES) analysis showed that most of the europium ions were in the 3+ oxidation state. The CIE 1931 chromaticity investigation shows the x,y color coordinates at (0.645, 0.351) in the reddish-orange region. To optimize the doping concentration of Eu2O3, it was determined that a fixed concentration of 50 mol% RSGW created the most suitable mixture. Both luminescence emission spectra exhibit strong luminescence, with a peak emission wavelength of 615 nm (⁵D0→⁷F2), confirming concentration quenching in both photoluminescence and x-ray luminescence at a concentration of 1.0 mol%. The study explores potential applications of this novel material in photonics and suggests that this eco-friendly synthesis approach holds great promise for sustainable and efficient production of reddish-orange emission materials.

Computational and optoelectronic investigations of red-emissive europium (III) β-diketonate with n-donor ligands for display applications

Europium complexes exhibiting red luminescence were prepared by employing β-diketone as main ligand and 1,10-phenanthroline as an additional ligand. Various methods, including 1H NMR, IR spectroscopy and analysis of optical band gap were employed to examine these complexes. The luminescent photophysical properties were investigated using PL spectroscopy and theoretical calculations were conducted to explore radiative transitions probabilities and Judd-Ofelt (J-O) parameters for transitions of type 5D0 → 7F2, 4. J-O parameters were determined using the JOES computer program and results were in good agreement with the outcomes obtained experimentally. The luminescence analysis results have verified the vibrant, single-color red emission of the prepared complexes. The band gap of ternary europium complexes, determined optically, electronically, and theoretically, falls within the range of 3–4 eV. This similarity indicates that these complexes are potentially suitable as semiconductor materials. The results from absorption, electrochemical and photophysical analyses indicate the potential use of synthesized complexes in lighting and display applications.

Study of structural and optical properties of Gd doped ZnO nanostructures synthesized by one-step, mass-scale productive method

In the present work, one-step, mass-scale productive solid state reaction method has been employed for the preparation of gadolinium (Gd) doped ZnO (GZOx: x = 0, 2, 4, 6, 8 wt%) nanostructures. The prepared GZOx samples have been studies their structural, morphological, elemental diffusion profile and optical properties using P-XRD, FE-SEM, EDS, FTIR, and photoluminescence (PL) spectroscopy. The powder X-ray diffractometer (P-XRD) results clearly indicate strong and sharp diffraction peaks with broadening that confirms the formation of hexagonal nanocrystalline structure of ZnO and Gd doped ZnO. The hexagonal morphology formation of the grains after doping of Gd contents into the ZnO nanostructures system is seen from the FE-SEM micrographs and the sizes of the grains are found to close to the results obtained from XRD patterns. The presence of Gd contents in ZnO matrix confirms its doping by EDS spectrum of 4 wt% Gd doped ZnO nanostructures. Fourier transform infrared (FTIR) results confirm the presence of functional groups and chemical bonding of ZnO at room temperature. Investigation of optical emission is interesting and the PL spectra reveal two emission peaks, one in UV-region located in the range of ∼385 to 395 nm and other is defects related emission centred at ∼450, ∼468, ∼503 and ∼562 nm in visible region for all the samples. The enhanced PL intensity is observed in the higher doped Gd contents in ZnO nanostructures and can be attributed to the presence of Gd ions into ZnO lattice. The detailed structural and luminescence analysis has been carried out and correlated. The study of structural and optical properties GZOx samples suggest the luminescent optoelectronic applications.

Real-time monitoring of CdTe quantum dots growth in aqueous solution

Quantum dots (QDs) are remarkable semiconductor nanoparticles, whose optical properties are strongly size-dependent. Therefore, the real-time monitoring of crystal growth pathway during synthesis gives an excellent opportunity to a smart design of the QDs luminescence. In this work, we present a new approach for monitoring the formation of QDs in aqueous solution up to 90 °C, through in situ luminescence analysis, using CdTe as a model system. This technique allows a detailed examination of the evolution of their light emission. In contrast to in situ absorbance analysis, the in situ luminescence measurements in reflection geometry are particularly advantageous once they are not hindered by the concentration increase of the colloidal suspension. The synthesized particles were additionally characterized using X-ray diffraction analysis, transition electron microscopy, UV-Vis absorption and infrared spectroscopy. The infrared spectra showed that 3-mercaptopropionic acid (MPA)-based thiols are covalently bound on the surface of QDs and microscopy revealed the formation of CdS. Setting a total of 3 h of reaction time, for instance, the QDs synthesized at 70, 80 and 90 °C exhibit emission maxima centered at 550, 600 and 655 nm. The in situ monitoring approach opens doors for a more precise achievement of the desired emission wavelength of QDs.

Recent Advances in Detection of Hydroxyl Radical by Responsive Fluorescence Nanoprobes.

Hydroxyl radical (•OH), a highly reactive oxygen species (ROS), is assumed as one of the most aggressive free radicals. This radical has a detrimental impact on cells as it can react with different biological substrates leading to pathophysiological disorders, including inflammation, mitochondrion dysfunction, and cancer. Quantification of this free radical in-situ plays critical roles in early diagnosis and treatment monitoring of various disorders, like macrophage polarization and tumor cell development. Luminescence analysis using responsive probes has been an emerging and reliable technique for in-situ detection of various cellular ROS, and some recently developed •OH responsive nanoprobes have confirmed the association with cancer development. This paper aims to summarize the recent advances in the characterization of •OH in living organisms using responsive nanoprobes, covering the production, the sources of •OH, and biological function, especially in the development of related diseases followed by the discussion of luminescence nanoprobes for •OH detection.

COMPARATIVE CHROMATOGRAPHIC AND SPECTRAL STUDY OF THE ALKALOID COMPOSITION OF THE BIOMASS OF TISSUE CULTURE AND THE HERB OF GLAUCIUM FLAVUM

Introduction. The culture of plant cells and tissues is an effective technology for obtaining various secondary metabolites, including for use in the pharmaceutical industry. Compounds synthesized in callus and suspension cultures may be identical to plant ones, and the yield of secondary metabolites, in some cases, exceeds plant sources. In this regard, yellow hornpoppy (Glaucium flavum Crantz.) is of great interest, containing glaucin, which has a unique antitussive effect and is a source of a number of medications. The purpose of this study is a comparative phytochemical study of the alkaloid composition of the tissue culture and the herb of Glaucium flavum. Material and methods. Callus tissue cultures of yellow hornpoppy yellow hornpoppy (Glaucium flavum Crantz.) were obtained in the laboratory of the Institute of Pharmacy of Kazan State Medical University. The herb of the Glaucium flavum cultivated on the territory of the Botanical Garden of Samara University was collected during the flowering period of plants in 2021. A comparative study of the alkaloid composition of the callus culture and the herb of Glaucium flavum was carried out by methods of luminescent microscopy on an Altami LUM-2 microscope (Russia), thin-layer chromatography (TLC) on Sorbfil-PTSH-AF-A-UV plates, as well as spectrophotometry. A mixture of solvents n-butanol-acetic acid-water 4:1:2 was used as a solvent system. The detection of separated substances was carried out by scanning chromatographic plates in UV light at a wavelength of 366 and 254 nm, followed by the manifestation of Dragendorf reagent. The identification of the isolated glaucin hydrochloride was carried out on the basis of UV, 1H-NMR, 13C-NMR spectroscopy data. 1H NMR spectra were obtained on the "JNM-ECX 400" device (399.78MHz), 13C NMR spectra were obtained on the "JNM–ECX 400" device (100.52 MHz). The spectra were recorded using a Specord 40 spectrophotometer (Analytik Jena AG, Germany) in the wavelength range of 190-500 nm. Results. During the luminescent analysis of the tissue culture of the Glaucium flavum Crantz., as well as intact plants, the type of luminescence characteristic of isoquinoline alkaloids was noted. Using TLC analysis, isoquinoline alkaloids, including glaucin, were found in samples of callus cultures and the aerial parts of Glaucium flavum, however, a lower glaucin content was noted in the sample of the callus culture compared to that of the intact plant. The spectrophometric analysis of the studied samples showed that the nature of the absorption curve in intact plants and crops of the so-called Glaucium flavum has both common and distinctive features. The UV spectrum of water-alcohol extraction from a sample of Glaucium flavum tissue culture has a similar spectrophotometric profile, however, it contains only one absorption maximum (288 nm), coinciding with that of the UV spectrum of water-alcohol extraction from the herb of this plant. Conclusions. Therefore, the final conclusion regarding the content of glaucin in the studied samples can be made only during the preparative isolation of substances from the biomass of Glaucium flavum using column chromatography