Search Results (71)

Micro- and nanoplastics (MNPs) are emerging environmental contaminants of increasing relevance to human health. Growing evidence suggests that, following ingestion, inhalation, or, less convincingly, dermal exposure, MNPs may cross biological barriers, enter lymphatic and vascular compartments, and reach the liver. Owing to portal blood flow, sinusoidal architecture and Kupffer cell activity, the liver appears to be one of the principal sites of early particle sequestration. Human biomonitoring, ex vivo and postmortem studies have detected MNPs in blood and multiple organs, including the liver, although the currently available evidence remains limited and methodologically heterogeneous. Their identification relies on multistep analytical procedures that integrate sample pretreatment with FTIR, Raman spectroscopy, LD-IR, Py-GC-MS and supplementary imaging methods. However, each of these techniques presents significant limitations, particularly in the analysis of nanoplastics. Experimental studies indicate that MNPs may induce hepatic injury through oxidative stress, mitochondrial impairment, endoplasmic reticulum stress, inflammation, DNA damage, dysregulated lipid metabolism and disruption of the gut–liver axis, consequently contributing to steatosis, cholestatic anomalies and fibrosis. Consequently, MNPs should be considered potential contributors to liver pathology, although more comprehensive human data are still required. Full article

Mitochondria play a crucial role in cellular bioenergetics, signaling, and metabolism; yet, many fundamental mechanisms such as the proton transfer along the membranes, the link between membrane curvature and oxidative phosphorylation, and the nanoscale organization of enzyme supercomplexes remain poorly understood due to the limitations of classical biochemical approaches. This review addresses this gap by systematically analyzing the contemporary physical methods used to investigate the mitochondrial structure and function from the micro to nano scale. It covers advanced fluorescence and super-resolution microscopy, electron and volume electron microscopy, and scanning probe techniques, as well as cryo-electron tomography for resolving supramolecular assemblies in near-native conditions. The review highlights the applications of the modern fluorescent probes, expansion and phase microscopy, and machine-learning-based image analysis for a quantitative assessment of the mitochondrial morphology, membrane potential, and dynamics in living cells and tissues. Complementary spectroscopic and scattering methods, including Raman spectroscopy, NMR, and X-ray and neutron scattering, are discussed as tools for probing the redox state, metabolite composition, and membrane organization. Emphasis is placed on integrating high-resolution experimental data with advanced computational frameworks to test competing models of mitochondrial function and pathology, and to guide the development of biomimetic and biomedical technologies. Full article

Two folding screens by futurist artist Giacomo Balla (1871–1958) in the collection of the Kröller-Müller Museum (the Netherlands) were investigated: Paravento con linea di velocità (1916–1917) and Paravento (1916/1917–1958). The screens are painted on both sides, the first on four canvases, stretched onto two wooden strainers and framed with painted wooden strips, and the second on wooden panels set into four painted stiles. In the past, damages on Paravento con linea di velocità were restored by conservators, while Paravento was probably first reworked by the artist himself and later restored by conservators. Yellowed varnish and discolored retouches on both screens led to a wish for treatment. The aim of this research was to gain insight into the painting techniques, layer buildup, pigments, binders, and varnishes of the two artworks. This information supported the decision making for treatment, and it broadens the knowledge on the materials used by Balla. Up to now, only a few published studies deal with the technical examination of paintings by this artist. Both folding screens were subjected to technical photography (UV, IR photography, and X-ray) and were examined with portable point X-ray fluorescence (pXRF) and Raman spectroscopy. Moreover, samples were taken. Cross-sections were studied with optical microscopy, scanning electron microscopy with energy-dispersive X-ray spectroscopy (SEM-EDX), attenuated total reflection Fourier-transform infrared (ATR-FTIR) imaging, and micro-Raman spectroscopy. Loose samples were examined with SEM-EDX, FTIR and micro-Raman spectroscopy, and pyrolysis gas chromatography mass spectrometry (Py-GC/MS). For Paravento con linea di velocità, all pigments and fillers of the painted canvases are compatible with the dating of the screen (1916–1917), but they differ from those on the frame. Here, rutile, in combination with various pigments, among which are blue copper phthalocyanine (PB15) and other synthetic organic pigments, was found. This indicates that the frame has been painted later, likely after the Second World War. The composition of the binders differs as well. Drying oil and pine resin have been used on the canvases, explaining the smooth and glossy appearance and solvent-sensitivity of the paint. On the frame, oil with some alkyd resin was identified. The provenance of the screen before 1972 is not clear, nor when the frame was made and painted and by whom. The results for Paravento indicate that the palettes of the two sides—painted in different styles—are comparable. Mainly inorganic pigments were found, except for the dark red areas, where toluidine red (PR3) is present. pXRF showed high amounts of zinc; cross-sections revealed that zinc white is present in the lower layers. These pigments are compatible with the dating of the screen (1916–1917). In many of the upper paint layers though, except for some green, dark red, and black areas, rutile has been identified. This indicates that these layers were applied later, likely after the Second World War. Since this folding screen was used by the artist and his family until his death in 1958, it seems likely that Balla himself reworked the screen. Full article

While existing studies on Guatemalan jadeite have predominantly focused on green varieties, the coloration mechanisms and origin of its blue counterparts remain poorly understood. Therefore, the present study provides the first comprehensive investigation of the Guatemalan blue jadeite using an integrated analytical approach, which combines Raman spectroscopy, micro X-ray fluorescence (µ-XRF), electron microprobe analysis (EMPA), X-ray diffraction (XRD), UV-Vis spectroscopy, and Cathodoluminescence (CL) imaging on seven representative samples. The results demonstrate that these jadeites consist of two distinct phases: a primary jadeite phase (NaAlSi₂O₆) and a secondary omphacite that form by metasomatic alteration by Mg-Ca-Fe-rich fluids. Spectroscopic analysis reveals that the blue coloration is primarily controlled by Fe³⁺ electronic transitions (with characteristic absorption at 381 nm and 437 nm) coupled with Fe²⁺-Ti⁴⁺ intervalence charge transfer, supported by μ-XRF mapping showing strong Fe-Ti spatial correlation with color intensity. CL imaging documents a multi-stage formation history involving initial high-pressure crystallization (Jd-I) followed by fluid-assisted recrystallization forming Jd-II and omphacite. The detection of CH₄, CO and H₂O in the fluid inclusions by Raman spectroscopy indicates formation in a serpentinization-related reducing environment, while distinct CL zoning patterns confirm a fluid-directed crystallization (P-type) origin. These findings not only clarify the chromogenic processes and petrogenesis of Guatemalan blue jadeite but also establish key diagnostic criteria for its identification, advancing our understanding of fluid-derived jadeite formation in subduction zone environments. Full article

Plant gums have long served as essential binding media in polychrome cultural heritage, contributing to pigment adhesion, surface cohesion, and long-term stability. This review evaluates recent advances in analytical technologies, including FTIR, Raman spectroscopy, GC-MS, LC-MS/MS, MALDI-TOF MS, hyperspectral imaging, and immunological assays, for the identification of gums such as gum arabic, peach gum, and tragacanth in diverse cultural contexts. Drawing on case studies from 19th-century watercolours, ancient Egyptian coffins, and Maya murals, the paper demonstrates how these methods enable precise chemical characterization even in complex, aged, and mineral-rich matrices. Such information directly aids conservators in selecting compatible restoration materials, tailoring treatment protocols, and assessing deterioration mechanisms. Persistent challenges remain, including gum degradation, spectral interference from pigments and restoration materials, sample heterogeneity, and limited reference libraries, particularly for non-European species. Future research directions emphasize multi-modal, non-invasive workflows that integrate hyperspectral imaging with spectroscopic and chromatographic methods, drone-assisted micro-Raman for inaccessible surfaces, machine learning-assisted spectral databases, and bio-inspired adhesives replicating historical rheology. By linking molecular identification to conservation decision-making, plant gum analysis not only deepens our understanding of historical material practices but also strengthens the scientific basis for sustainable heritage preservation strategies. Full article

Graphene, a two-dimensional carbon material, possesses exceptional properties such as high electron mobility, exceptional strength that surpasses that of steel, chemical resistance, environmental friendliness, and a large specific surface area. In this study, we used the modified Hummer process to produce graphene oxide, which was applied to an aluminum alloy substrate as a corrosion-resistant coating. The aluminum alloy used in our study is AA2024, which is widely applied in industry and aircraft. The coating layer was characterized by micro-Raman spectroscopy and atomic force microscopy (AFM) before and after the reduction process. Micro-Raman spectroscopy provided information on the degree of reduction and the presence of functional groups in the coating layer. AFM images enabled the study of surface morphology and topography. After the reduction process, achieved by annealing in an argon atmosphere at 140 °C, micro-Raman spectroscopy and AFM were again used to assess structural and morphological changes. The reduction resulted in the formation of reduced graphene oxide (RGO), which exhibited improved conductivity and stability. The combination of micro-Raman spectroscopy and AFM characterization techniques provided detailed information on the properties and effectiveness of the coating layer. This research contributes to developing anti-corrosion methods using advanced materials and surface engineering techniques. Full article

In this study, a lamella prepared using focused ion beam (FIB) milling from a magnesium–silver alloy wire was investigated. The wire, intended for biomedical applications, was initially degraded in simulated body fluid (SBF) under physiological conditions. Raman spectroscopy was performed across the entire FIB specimen and the results were correlated with findings from scanning transmission electron microscopy (STEM). Our micro-Raman analysis identified chemical compounds at distinct regions within the specimen. Dominant Raman modes at ~1350 cm⁻¹ and ~1590 cm⁻¹, likely derived from elemental carbon from the FIB protection layer, were observed. Additionally, modes indicative of the alloy’s interaction with SBF, attributable to the constituents of SBF, were detected. Notably, Raman modes at ~3650 cm⁻¹ corresponding to the OH stretching mode were identified in the targeted areas of the lamella, highlighting the chemical interaction between magnesium (Mg) and the SBF. The micro-Raman mapping images showed localized Mg(OH)₂ distributions, which correlated strongly with the STEM analyses. This study underscores the effectiveness of correlating Raman spectroscopy, revealing chemical changes and STEM, capturing the corresponding microstructural changes. The combined approach is crucial for a deeper understanding of material degradation and reactivity in biocompatible alloys under physiological conditions and advances the characterization of biocompatible materials in physiological environments. Full article

Here in this work, we report on micro-Raman spectroscopy investigations performed on freestanding Ni-rich NCM (Li_xNi_0.83Co_0.11Mn_0.06O₂) microcrystals transferred to flexible polyethylene terephthalate (PET) host substrates. This technological procedure introduces a first building block for future on-chip-integrated micro-accumulators for applications in flexible optoelectronics, sensors, microbiology, and human medicine. An after-synthesis thermal treatment was used to help improve the material homogeneity and perfection of the cathode material. To this end, a local laser micro-annealing process was applied to the freestanding Ni-rich NCM microcrystals. The thermally initialized structural processes in the singular micro-cathode units were characterized and determined by micro-Raman spectroscopy. Micro-Raman mapping images revealed the evolution of a recrystallization process after the local annealing procedure. Furthermore, laser micro-annealing led to the suppression of the pristine “polycrystalline morphology” of the investigated micro-cathode regions. Besides the dominant characteristic Raman mode at ~1085 cm⁻¹, most likely ascribed to lithium carbonate, metal oxides with Raman modes around ~550 cm⁻¹ were identified. This highly efficient transfer and integration technology represents a basic building block towards micrometer-sized accumulators for a large range of emerging applications. Full article

A method for identifying six estrogen preparations by thin-layer chromatography combined with Raman imaging microscopy (TLC-RIM) was established. An appropriate pretreatment method was adopted to extract and purify the six estrogen preparations. After that, each estrogen extraction solution was spotted on a thin-layer chromatography plate. Estriol (E3), estradiol (E2), estradiol valerate (EV), estradiol benzoate (EB), nilestriol (CEE), and ethinylestradiol (EE2) were separated by TLC, and their R_f value and localization were determined under a UV lamp at 254 nm, followed by the in situ enrichment of the drug component. Using a 532 nm laser as the light source, the Raman scattering spectrum of the component was directly collected by micro-Raman imaging. The R_f values after TLC separation of the six estrogens and their Raman spectra can, respectively, reflect differences in polarity and structure, and they are not affected by the excipients of preparation. The detection limits of the six estrogens are 0.636, 1.00, 0.687, 0.497, 0.649, and 0.626 mg/mL. Based on the intensity of the minimum characteristic peak, the stability results within 40 min showed that the RSD of each substance is 1.34, 2.06, 1.65, 3.99, 1.16, and 2.71%, respectively. This method has strong specificity, good stability, and high sensitivity, and it can provide a new reference for improving the identification standards of estrogen preparations. Full article

The ancient Roman town of Turris Libisonis was located on the northern coast of Sardinia and was known in the past as an important naval port. Located in the Gulf of Asinara, it was a Roman colony from the 1st century BCE and became one of the richest towns on the island. Among the archaeological finds in the area, the cippus exhibited in the Antiquarium Turritano is of great interest for its well-preserved traces of polychromy. The artefact dates back to the early Imperial Age and could have had a funerary or votive function. The artefact was first examined using a portable and non-invasive protocol involving multi-band imaging (MBI), portable X-ray fluorescence (p-XRF), portable FT-IR in external reflectance mode (ER FT-IR) and Raman spectroscopy. After this initial examination, a few microfragments were collected and investigated by optical microscopy (OM), X-ray powder diffraction (XRPD), Fourier-transform infrared spectroscopy in ATR mode (ATR FT-IR) and micro-ATR mode (μATR FT-IR) and Scanning Electron Microscopy/Energy Dispersive Spectroscopy (SEM-EDS) to improve our knowledge and characterize the materials and to determine their provenience. The results contribute to a better understanding of the provenance of materials and shed light on pigments on stone and their use outside the Italian peninsula and, in particular, Roman Sardinia. Full article

The Hispanic Society Museum & Library (HSML) holds a collection of nine viceregal barniz de Pasto objects, made by Indigenous artisans in the 17th and 18th centuries. Designed to imitate Asian lacquers and intended for European aesthetic tastes, barniz de Pasto is an example of Indigenous technique and knowledge that has survived to the present day. An in-depth analysis of five of these barniz de Pasto objects, dated to the first half and last quarter of the 17th century based on their iconography, was carried out through a combination of non-invasive and micro-invasive techniques, including portable X-ray fluorescence (pXRF) spectroscopy to investigate the possible presence of inorganic pigments, and fiber-optics reflectance spectroscopy (FORS) and reflectance imaging spectroscopy (RIS) to provide molecular information on colorants and their distributions across the objects. Dyes and pigments were also identified using Raman spectroscopy, Fourier-transform infrared (FTIR) spectroscopy, and liquid chromatography/mass spectrometry (LC/MS). The nature of the resin was determined by FTIR and pyrolysis-gas chromatography/mass spectrometry (Py-GC/MS), while the decoration stratigraphy and composition were analyzed by scanning electron microscopy with energy-dispersive X-ray spectroscopy (SEM-EDS). This paper confirms the use of mopa mopa, the resin used in the barniz de Pasto technique, in two objects not previously analyzed, and identifies indigo, insect-based red, calomel, lead white, and an unknown flavonol-based yellow dye, and challenges the use of calomel as a temporal marker for these works. Taken together, these results expand our understanding of the material use and explorations undertaken by artists during this time period to create such elaborate and enduring objects. Full article

Nephrite is a very precious gemstone material. As a non-renewable resource, the discovery of new nephrite deposits and the study of the genesis of nephrite have aroused great interest. A new occurrence of nephrite known as Xinyu nephrite was discovered in Xinyu Country, Jiangxi province, China. Field investigations reveal that nephrite appears in a contact zone between the Mengshan composite granitic pluton and Permian carbonate rock. The carbonate rock is calcic marble that underwent diopsidization and tremolitization. Nephrites have a light yellow-green color, weak greasy luster, are slightly-translucent to translucent, and are fine-grained. Their refractive index (RI) ranges from 1.60 to 1.61, and their specific gravity (SG) value ranges from 2.90 to 2.91, falling within the range of nephrites from Xinjiang, China. Their Mohs hardness (Hm) ranges from 5.78 to 5.83. Petrographic observations and electron probe micro analyzer (EPMA) data indicated that analyzed nephrites mainly comprise tremolite, with minor diopside, calcite, quartz, and apatite. Tremolite has a ratio of Mg/(Mg + Fe²⁺) greater than 0.99. The tremolite grains show microscopic fibrous-felted and columnar textures. Scanning electron microscope (SEM) images show some tremolite fibers interwoven in different crystallographic orientations, and some arranged in parallel. Fourier transform infrared and Raman spectroscopy features reveal the bands of minerals typical for nephrite composition. The petrographic characteristics and geological background of the Mengshan area indicate that nephrite formed through a replacement of calcic marble, which differs from the two known types (D-type: dolomite-related; S-type: serpentinite-related). Mineral replacements were common in nephrite, including diopside by tremolite, calcite by tremolite, and recrystallization of coarse by fine tremolite grains. The discovery of Xinyu nephrite occurrence complements the resource and provides an updated case for the in-depth study of the diversity of nephrite deposits. Full article

The presence of microplastics in soil has become a significant global concern, posing a threat to environmental, agricultural, and human health. However, the use of various detection methods has led to significant discrepancies in the statistics reported for the abundance of soil microplastics across the available literature, resulting in poor comparability across the available literature. Studies have shown that plastic film residue is among the main primary sources of microplastics in farmland soils. Therefore, we manufactured and selected polyethylene microplastics (PE-MPs) from plastic film and combined them with soil samples after density separation treatment, forming a spiked test soil sample, which was subjected to density separation and extraction using a ZnCl₂ solution. The experiment used visual inspection by stereo microscopy, micro-Fourier transform infrared spectroscopy, micro-Raman spectrometry, laser direct infrared imaging, and pyrolysis-gas chromatography–mass spectroscopy for the quantitative analysis of spiked soil. This study systematically assessed and compared these five common soil microplastic detection methods. The results revealed different quantitative detection accuracies across various particle size ranges. Micro-Fourier transform infrared spectroscopy showed a broader applicable particle size range (20–5000 μm) and higher detection rate (91%), while the detection range (>50 μm) and rate (70%) of visual inspection through stereo microscopy were lower. For the identification of microplastic morphology, laser direct infrared imaging performed better, whereas micro-Fourier transform infrared spectroscopy had the advantage in determining the types of polymers present over micro-Raman spectrometry. The advantages, disadvantages, and detection rates of the above five detection methods were clarified during the detection process. Considering these findings and similar studies, we suggest three combinations of the evaluated methods to optimize the detection of PE-MPs. Full article

The Hebrew Scroll, catalogued as Magliabekian Manuscript III 43 and belonging to the National Central Library of Florence (BNCF), is a membranous richly decorated scroll, with colorful depictions of sacred sites through the Holy Land to Lebanon along with handwritten texts in Hebrew and notes in Italian. Despite the fact that the manuscript was originally catalogued as an “object of no artistic or scientific value”, recent paleographic studies dated it to the XIV century and highlighted it as the oldest scroll still available, depicting holy places from Egypt to Lebanon. Nevertheless, precise dating, authorship, and the interpretation of its original function are still uncertain. A suite of complementary techniques was used, including photographic documentation in visible (VIS) light in diffuse light, grazing light, and transillumination, luminescence induced by ultraviolet (UV) radiation, imaging spectroscopy (IS), Macro Area X-ray Fluorescence (MA-XRF), and spot analyses such as fiber-optic reflectance spectroscopy (FORS) in the UV, VIS, and near-infrared (NIR) regions, Fourier transform infrared spectroscopy (FT-IR) in external reflectance mode (ER), and micro-Raman spectroscopy. The results of the non-invasive diagnostic campaign enabled the identification of several constituting materials (parchment, pigments, binder, and inks). The identified materials were consistent with the proposed dating and geographical manufacturing area of the artefact. Full article

A limestone relief fragment with a figure in a winged disk from the fifth-century BCE Hall of 100 Columns at Persepolis in southwestern Iran that entered the Harvard Art Museums’ collections in 1943 preserves significant traces of its original coloration and has played a key role in the rediscovery of polychromy at the Achaemenid Persian capital. After tracing the fragment’s journey to Cambridge, MA, this article presents the results of recent technical studies of its pigment remains, including visible light-induced infrared luminescence (VIL) imaging, X-ray fluorescence (XRF) spectroscopy, and the analysis of micro samples by Raman spectroscopy, Fourier transform infrared (FT-IR) spectroscopy, scanning electron microscopy (SEM), and polarizing light microscopy (PLM). The new scientific data is compared to the findings of ongoing investigations of polychromies at Persepolis and other Achaemenid Persian sites and evaluated for the information it can and cannot provide on the original appearance of the figure in the winged disk, likely the Zoroastrian god Ahuramazda. The article reviews past attempts at reconstructing the relief’s coloration and the assumptions that guided them, recounts the experience of creating a tangible three-dimensional color reconstruction for an exhibition, and concludes with some general thoughts on the valuation of colorfulness. Full article