Search Results (1,881)

ISO 22002-100:2025 introduces stringent and more technically explicit prerequisite programme (PRP) requirements for allergen management, food fraud mitigation, and the control of chemical and packaging-related contaminants across the food, feed, and packaging supply chain. This review examines how advanced chromatographic methods provide the analytical basis required to meet these requirements and to support alignment with GFSI-recognized certification schemes. Recent applications of liquid and gas chromatography coupled with mass spectrometry for allergen quantification, authenticity assessment, and the determination of packaging migrants, auxiliary chemical residues, lubricants, and indoor pest-control pesticides are presented to demonstrate their relevance as verification tools. Across these PRP-related controls, chromatographic methods enable trace-level detection, structural specificity, and reproducible measurement performance, thereby shifting PRP compliance from a documentation-based activity to a process verified through measurable analytical evidence. The review highlights significant progress in method development and simultaneous multi-target analytical approaches while also identifying remaining challenges related to matrix-appropriate validation, harmonization, and analytical coverage for chemical contamination, which is now formally defined as a measurable PRP requirement under ISO 22002-100:2025. Overall, the findings demonstrate that chromatographic analysis has become essential to demonstrating PRP effectiveness under ISO 22002-100:2025, supporting the broader shift toward evidence-based, scientifically robust food safety assurance. Full article

Alzheimer’s disease (AD) is a prevalent neurodegenerative condition that progressively impairs cognitive processes, particularly learning and memory. A key pathological feature of AD involves senile plaques mainly composed of β-amyloid (Aβ) peptides, generated via the amyloidogenic pathway from amyloid precursor protein (APP) through sequential β-secretase (BACE1) and γ-secretase cleavage, positioning BACE1 inhibition as a prime therapeutic target. In this study, we applied bioassay-guided fractionation of the butanol-soluble fraction from Dryopteris crassirhizoma rhizomes, previously reported to inhibit Aβ production, to isolate and characterize Aβ-lowering constituents. Through successive chromatographic steps, nine compounds were isolated and structurally classified into flavonoids, chromones, and phloroglucinols, including epicatechin (1), β-carboxymethyl-(-)-epicatechin (2), 7-methoxy-isobiflorin (3), biflorin (4), eriodictyol (5), noreugenin (6), phloroglucinols (butyrylphloroglucinol (7), 2-propionyl-4-methylphloroglucinol (8), and 2-butyryl-4-methylphloroglucinol (9) by comprehensive spectroscopic analysis (NMR, MS, UV, IR). These compounds were assessed for effects on sAPPβ and BACE1 (β-secretase) levels by Western blot, with Aβ production quantified via ELISA in a cellular AD model (APP-CHO cells). Compounds 5–9 significantly reduced sAPPβ and BACE1 expression while potently suppressing Aβ generation. These results demonstrate that diverse constituents from D. crassirhizoma rhizomes inhibited Aβ production through BACE1 suppression, highlighting their potential as natural lead compounds for AD prevention or therapy. Full article

Although numerous baseline correction methods exist, most are confined to static post-elution processing and fail to meet real-time analysis requirements. To address this, we propose a real-time baseline estimation method based on the Informer time-series prediction model that performs correction during data acquisition without waiting for complete elution. Our work focuses on three key aspects: chromatographic dataset construction, model training, and baseline prediction. Simulation experiments demonstrate that the proposed method achieves comparable accuracy to conventional static processing approaches while exhibiting significant real-time advantages. In processing real chromatographic data, the model achieves a 98.3% chromatographic peak retention rate, with a single computation time of approximately 35 ms—substantially shorter than typical chromatographic sampling cycles (600–900 ms), thus fully satisfying the quantitative analysis requirements for real-time background subtraction. Full article

Milk fat globule membrane (MFGM) phospholipids could promote the development of infants’ brain, nervous system and digestive system. This research conducted a comparative analysis of phospholipid composition in MFGM of colostrum from different bovine species (Holstein cattle, yak, and Buffalo), with a particular focus on analyzing phospholipid variations in yak MFGM across different lactation stages. Chromatographic quantification revealed phosphatidylcholine (PC) as the predominant phospholipid class (34.7–47.44%) in all examined species. Notably, Holstein cow milk contains significantly higher levels of phosphatidylethanolamine (PE). Distinct phospholipid profiles emerged between species: yak milk demonstrated significantly higher concentrations of sphingomyelin (SM), lysophosphatidylethanolamine (LPE), dimethylphosphatidylethanolamine (dMePE), and bis-methylphosphatidic acid (BisMePA), whereas buffalo milk showed preferential accumulation of phosphatidylinositol (PI), phosphatidylserine (PS), phosphatidylglycerol (PG), and lysophosphatidylcholine (LPC). Longitudinal analysis revealed dynamic changes in yak milk phospholipids during lactation: as the lactation period in-creases, PC, PS, LPC, LPE, methylphosphatidylcholine (MePC), BisMePA, and dMePE exhibited progressive decline, while PE, SM, PI and PG showed incremental increases. Analysis of phospholipid metabolism pathways indicates that yak colostrum supports early calf development by enriching phospholipids associated with immune and neuroprotection, while mature milk shifts toward maintaining membrane stability. These compositional characteristics position yak milk as a promising phospholipid-fortified alternative to human breast milk. Full article

Silica-based sorbents covalently modified with polyhedral boron clusters represent a promising platform for highly selective separation materials, yet robust and synthetically accessible immobilization protocols remain underdeveloped. In this work, novel sorbents based on commercially available silica gels functionalized with closo-dodecaborate anions were synthesized and systematically characterized. Two immobilization strategies were compared: direct nucleophilic addition of surface aminopropyl groups to the nitrilium derivative (Bu₄N)[B₁₂H₁₁NCCH₃] and sol–gel condensation of a pre-formed boron-containing APTES-derived silane. Covalent attachment via amidine bond formation was confirmed by solution and MAS ¹¹B NMR spectroscopy, IR spectroscopy, elemental analysis/ICP-OES, and SEM. The direct grafting route afforded a boron loading of 4.5 wt% (≈20% of the theoretical capacity), with the efficiency limited by electrostatic repulsion between anionic amidine fragments on the negatively charged silica surface, whereas the APTES route gave lower absolute loading (0.085 mmol/g) due to the low specific surface area of the coarse silica support. Despite the moderate degree of functionalization, the resulting boron cluster–modified silica gels are attractive candidates for specialized chromatographic applications, where the unique hydrophobic and dihydrogen-bonding properties of closo-dodecaborates may enable selective retention of challenging analytes and motivate further optimization of surface morphology and immobilization conditions. Full article

Copper-based catalysts have emerged as promising materials for electrochemical carbon dioxide reduction reactions, owing to copper’s unique ability to facilitate multi-electron transfer processes and produce valuable products such as methanol and ethanol. In this study, novel trisferrocenyltrithiophosphite–copper(I) bromide composites with Cu-to-ligand molar ratios of 1:1 and 2:1 were synthesized and evaluated for their catalytic performance. The composites were characterized by a combination of techniques, including powder X-ray diffraction (PXRD), linear sweep voltammetry (LSV), potentiostatic testing, chromatographic analysis, scanning electron microscopy (SEM) and X-ray photoelectron spectroscopy (XPS). Electrochemical measurements demonstrated significant current enhancements in the presence of CO₂, highlighting the composites’ catalytic activity. Potentiostatic tests revealed excellent stability, with only a 9% decline in current density over 5 h of electrolysis. Product analysis via gas chromatography indicated the formation of methanol for the 1:1 composite and ethanol for the 2:1 composite with Faradaic efficiencies of 5.79% and 9.26%, respectively. While absolute efficiencies remain modest due to competitive hydrogen evolution, these results demonstrate a tunable catalytic performance based on the Cu-to-ligand ratio. SEM and XPS studies further supported the formation of active catalytic centers and changes in the oxidation states of copper during CO₂ reduction. PXRD analysis confirmed the retention of structural integrity for both composites before and after catalytic testing. Full article

Thin-layer chromatography (TLC) remains a widely used, cost-effective and convenient method to separate small molecules, particularly in the field of natural products and (phospho)lipids. Despite advances in chromatographic methods such as high-performance liquid chromatography (HPLC), TLC retains several advantages, including simplicity and accessibility. However, a critical step is the visualization of the separated lipids on the TLC plate. Although the majority of the regularly used methods were established decades ago, there are still a number of potential pitfalls and widely unknown aspects. This review provides a concise overview about commonly used stationary phases and the solvent systems in TLC analysis of lipids. The main focus is on visualization techniques, spanning from non-specific, destructive (charring by semi-concentrated acids) to specific, non-destructive approaches (e.g., exposition to iodine to monitor unsaturated lipids). The advantages and disadvantages of the different methods will be critically discussed and frequently occurring problems highlighted. Furthermore, the combination of TLC with mass spectrometry (MS) detection will be introduced, covering both extraction-based electrospray ionization MS techniques as well as desorption techniques such as matrix-assisted laser desorption/ionization MS. MS detection, while generally more sensitive and offering molecular specificity, introduces higher technical and financial requirements compared to conventional staining. Nonetheless, the combination of TLC with MS holds significant potential for enhancing lipidomic workflows, particularly in complex biological samples. Full article

Fire-retardant intumescent coatings offer an effective means of enhancing the fire resistance of combustible substrates such as wood. These coatings have a complex chemical composition and, when exposed to temperatures above 200 °C, undergo an intumescent reaction accompanied by the release of non-flammable gases, forming an expanded, charred layer with low thermal conductivity. This provides thermal insulation and acts as a physical barrier against heat, oxygen, and flammable volatiles. In this study, the applicability of several thermoanalytical techniques for evaluating the performance of three different intumescent coatings applied to spruce wood was investigated. Simultaneous thermogravimetric analysis (TGA) and differential scanning calorimetry (DSC) showed that coating No. 3 was the most efficient, initiating substrate protection at the lowest temperature and reducing the combustion enthalpy by approximately 50% compared to uncoated wood. DSC-microscopy visualization enabled direct observation of the intumescent expansion, degradation of the carbonized protective layer, and delayed thermal decomposition of coated wood. Furthermore, a comparison between TGA-MS and TGA-IST16-GC-MS demonstrated the superiority of chromatographic separation for identifying evolved gaseous products. While TGA-MS is effective for detecting small gaseous species (e.g., H₂O, CO₂, formaldehyde), TGA-IST16-GC-MS enables the deconvolution of many degradation products evolving simultaneously, allowing for distinction between flame-retardant-related species, polymer backbone fragments, nitrogen-rich heterocycles, and small oxygenated molecules in the most effective coating. Full article

Nutraceuticals are food-based products that provide health benefits beyond basic nutrition and play an increasingly important role in preventive healthcare. Ensuring their quality, safety, and efficacy is critical as the global market expands. A systematic literature search was conducted in Scopus, Web of Science, and PubMed using keywords such as ‘nutraceuticals,’ functional foods,’ and ‘quality control,’ with studies selected based on their focus on methods for standardization, characterization, and quality assessment. This review summarizes current analytical approaches, including spectroscopic, chromatographic, and techniques for elemental analysis, highlighting their applications in compound identification, quantification, detection of adulterants, and overall quality control. Emerging challenges and future trends, such as the integration of chemometrics and real-time analytical strategies, are also discussed, providing a comprehensive perspective on the evolving field of nutraceutical analysis. Full article

Neurotoxicity following South American Crotalus rattlesnake bite is primarily caused by crotoxin, the most abundant component in their venom. Despite the central role of voltage-gated calcium channels (Ca_V) in neurotransmission, direct targetability by crotoxin has been poorly explored. Crotoxin is a non-covalent heterodimer formed by an acidic subunit (CA) and a basic toxic phospholipase A₂ subunit (CB). Here, we chromatographically isolated the CB subunit from Crotalus vegrandis and studied its effect on Ca_V heterologously expressed in tsA201 cells using the whole-cell patch-clamp technique. Mass spectrometry analysis identified a protein that matched with 97% sequence coverage the CBc isoform from Crotalus durissus terrificus. Isolated CB exhibited moderate phospholipase activity that was not correlated to its cytotoxic effect on cultured tsA201 cells. Using Ba²⁺ as a charge carrier to prevent the enzymatic activity, we found that CB inhibited currents mediated by the N-type Ca_V2.2 and Ca_V1.2 L-type calcium channels, in a dose–dependent manner, with higher potency for the latter, and negligible changes in the voltage dependence of channel activation. Our results reveal a novel phospholipase-independent biological activity and a molecular target of CB providing new insights into the pathophysiology of Crotalus snakebite envenoming with potential clinical therapeutic implications. Full article

Ligustrum japonicum Thunb. (Oleaceae) has long been valued for the medicinal properties. Its fruits are traditionally utilized, while the leaves and branches are generally discarded after fruit harvest. These aerial parts therefore represent underutilized by-products whose phytochemical profiles remain insufficiently characterized. To elucidate the organ-specific chemical diversity and assess the potential value of these underutilized parts, a comparative analysis of the fruits, leaves, and branches was performed using HPLC–MS/MS combined with GNPS-based molecular networking, with a particular focus on secoiridoids, the characteristic metabolites of the Oleaceae family. This approach revealed substantial overlap as well as distinct variations in secoiridoid profiles among the three plant organs. Chromatographic separation yielded 14 secoiridoid derivatives shared across all organs. In addition, four previously undescribed secoiridoids were isolated and identified through spectroscopic analyses: secoligunosides A (1) and B (2) from the leaves and secoligunosides C (3) and D (4) from the branches. Among the major identified secoiridoids, oleuropein (10), 8Z-nüezhenide (17), and GL-3 (18) exhibited weak proliferative activity, showing an approximately 10–20% increase compared to control, on human dermal papilla cells. Collectively, these findings demonstrate that the leaves and branches not only contain key secoiridoids found in the fruits but also harbor unique metabolites, highlighting their value as alternative or complementary medicinal resources. The underutilized parts of L. japonicum therefore represent promising sources of natural products and warrant further investigation for future therapeutic applications. Full article

In this study, we developed a method for creating an active layer based on a composite material consisting of chitosan and an anisotropic network of nickel fibers (Chitosan/Ni + NiFs). Using this chitosan biopolymer matrix and anisotropic network, we achieved a high specific surface area for the catalytic material, high lateral conductivity for the layer, and stable characteristics, ultimately leading to increased overall electrocatalytic activity in the hydrogen evolution reaction (HER). Through linear voltammetry and impedance spectroscopy, we identified the mechanism and kinetics of the HER in the developed system. The overpotential of the electrochemical reaction was 213 mV at a current density of 10 mA/cm². Chromatographic analysis confirmed the effectiveness of the Chitosan/Ni + NiFs system in the HER. Our results show how the chitosan biopolymer matrix and oriented nickel fiber network influence charge transfer and electrode reactions, as reflected in the activation energies of hydrogen bonds on the electrocatalytic layers. These findings show that it is feasible to combine a biopolymer matrix and an anisotropic nickel fiber network to create effective electrocatalysts. This approach enables the development of environmentally friendly electrolytic hydrogen production technologies. Full article

The main goal of this study was to develop methods for quality control of naftifine hydrochloride in solution and cream forms, focusing on “Quantitative Determination” and “Related Impurities.” New, precise, accurate, and environmentally friendly high performance liquid chromatography (HPLC) methods were developed for the determination of naftifine hydrochloride and its impurities. “Quantitative determination” was performed using a diode array detector at 254 nm with an isocratic mobile phase (1.154 g of ammonium acetate R dissolved in 300 mL of water R, followed by the addition of 0.2 mL of glacial acetic acid R, mixed well) and methanol (30:70). The chromatographic columns Gemini C18 and Luna C18 were used. “Related impurities” were separated at 270 nm using a gradient mobile phase consisting of 10 M sodium octanesulfonate, 0.4 g/L disodium hydrogen phosphate anhydrous solution (pH 6.5), acetonitrile, and the Synergi Hydro-RP chromatographic column. The developed method, validated according to ICH guidelines, showed run times of 55 min for impurity analysis and 6 min for active ingredient determination. The methods were successfully applied to the quality control of the solution and cream. Full article

Micro- and nanoplastics (MNPs) are increasingly recognized as pervasive environmental contaminants with profound implications for ecosystems and human health. Their small size, compositional diversity, and occurrence across complex matrices—including water, soil, food, and biological samples—pose substantial analytical challenges. Conventional techniques such as vibrational spectroscopy, chromatographic analysis, and electron microscopy have yielded critical insights into MNP composition, morphology, and distribution; however, these methods often face limitations in sensitivity, throughput, and adaptability to real-world samples. Recent advances in nanotechnology have catalyzed the emergence of nanodevices—encompassing nanosensors, nanopore systems, integrated lab-on-a-chip platforms and nanostructured capture materials—that promise enhanced sensitivity, specificity, and the capacity for real-time, in situ detection. These innovations not only facilitate high-throughput analysis but also provide novel opportunities for integrated characterization of MNPs across diverse matrices. This review synthesizes the current state of nanodevice-based MNP detection, critically examining their principles, performance, and limitations relative to conventional approaches, and outlining the key needs for standardization, matrix-specific adaptation, and regulatory harmonization. Full article

Symphytum officinale L. (Boraginaceae) is a plant with proven anti-inflammatory and analgesic activity on the musculoskeletal system. The traditional use of comfrey primarily refers to its roots, although some literature also mentions the leaves as an alternative plant material. Comparing the therapeutic potential of both plant materials requires additional data on the chemical composition of S. officinale leaves and their biological properties. The aim of the study was to analyze polyphenols in comfrey leaves of different origins and to assess their antioxidant and anti-inflammatory potential against comfrey roots, also collected from different sources. Polyphenol profiles were recognized by 2D TLC and HPLC-DAD-ESI-MS methods, and quantitative analysis was performed by the HPLC-UV/Vis (high performance liquid chromatograph with-ultraviolet/visible detection) method. The antioxidant activity was assessed using DPPH (2,2-diphenyl-1-picrylhydrazyl), FRAP (ferric reducing antioxidant power), and ABTS (2,2′-azino-bis(3-ethylbenzothiazoline- 6-sulfonic acid) diammonium salt) assays, and for leaves also using the TLC-DB (thin layer chromatography-direct bioautography) technique with the DPPH radical. Chemometric analysis to assess the relationship between the antioxidant activity and the origin of comfrey plant raw materials was performed. Factor analysis (FA) confirmed that geographic origin and cultivation conditions influenced the antioxidant content of both plant raw materials. The study results indicate that comfrey leaves can substitute for comfrey roots containing not only caffeic acid derivatives but also flavonoids, and exhibiting stronger antioxidant activity. Full article