Analytica Chimica Acta, Год журнала: 2024, Номер 1335, С. 343456 - 343456
Опубликована: Ноя. 21, 2024
Язык: Английский
Analytica Chimica Acta, Год журнала: 2024, Номер 1335, С. 343456 - 343456
Опубликована: Ноя. 21, 2024
Язык: Английский
Water Research, Год журнала: 2025, Номер unknown, С. 123179 - 123179
Опубликована: Янв. 1, 2025
Язык: Английский
Процитировано
4Molecules, Год журнала: 2025, Номер 30(2), С. 364 - 364
Опубликована: Янв. 17, 2025
Emerging contaminants (ECs), encompassing pharmaceuticals, personal care products, pesticides, and industrial chemicals, represent a growing threat to ecosystems human health due their persistence, bioaccumulation potential, often-unknown toxicological profiles. Addressing these challenges necessitates advanced analytical tools capable of detecting quantifying trace levels ECs in complex environmental matrices. This review highlights the pivotal role mass spectrometry (MS) monitoring ECs, emphasizing its high sensitivity, specificity, versatility across various techniques such as Gas Chromatography-Mass Spectrometry (GC-MS), Liquid (LC-MS), High-Resolution Mass (HR-MS). The application MS has facilitated real-time detection volatile organic compounds, comprehensive non-targeted screening unknown contaminants, accurate quantification diverse matrices including water, soil, air. Despite effectiveness, matrix interferences, lack standardized methodologies, limited spectral libraries persist. However, recent advancements, hybrid systems integration artificial intelligence (AI), are paving way for more efficient predictive modeling contaminant behavior. Continued innovation technologies collaborative efforts essential overcome existing ensure sustainable solutions mitigating risks associated with emerging contaminants.
Язык: Английский
Процитировано
1Environments, Год журнала: 2025, Номер 12(1), С. 22 - 22
Опубликована: Янв. 12, 2025
Many pharmaceutical active compounds are prepared as hydrochlorides for quick release in the gastrointestinal tract upon oral administration. Their inadvertent escape into water environment requires efficient analytical separation accurate quantitation to monitor their environmental fate. The purpose of this study is demonstrate how best optimize a capillary electrophoresis method four model hydrochlorides. Concentration sodium dibasic phosphate background electrolyte solution, pH adjustment with HCl or NaOH, and applied voltage across were three key factors chosen optimization. peak resolutions total migration time examined response indicators complete central composite design surface methodology. examination revealed that CE was driven significantly by linear regression minimally quadratic model, based on coefficient determination, lack fit, sum squares, p values. Under optimal conditions concentration 75 mM, 9, 10 kV, separated within five minutes order metformin (first) > phenformin mexiletine ranitidine (last). limits UV detection/quantification attained under 0.015/0.045, 0.020/0.060, 0.142/0.426, 0.017/0.051, respectively.
Язык: Английский
Процитировано
0Analytical Chemistry, Год журнала: 2025, Номер unknown
Опубликована: Март 13, 2025
Characterizing the chemical exposome relies on advanced instrumentation including tandem mass spectrometry coupled to liquid chromatography (LC-MS/MS), and nontargeted analysis (NTA) using high-resolution MS. However, proper sample pretreatment, balancing broad analyte coverage, method robustness, throughput remain a major bottleneck in exposomics. Here, we developed robust scalable solid phase extraction (SPE) protocol for human urine plasma optimized it panel of 94 highly diverse environmental food-related contaminants (LogP −0.7 6.8). Extraction recoveries (RE) signal suppression enhancement (SSE) were determined targeted LC-MS/MS. Acceptable REs (60–140%) achieved >70% analytes, acceptable SSE values 86% 90% plasma, respectively. Subsequently, was transferred 96-well plate format, significantly improving meet capacity requirements needed exposome-wide association studies (ExWAS). The established workflow is approximately 10× faster than routinely used metabolomics-based protein precipitation approaches when comparing estimated total time 1000 samples. method's applicability NTA suspect screening tested compared generic NIST standard reference materials (SRM 3672) 1950). Favorable performance shown while SPE demonstrated promising results. thus not only superior future high-throughput exposomics but also offers an option applications. presented well-balanced approach applicable research fields pharmacology, food safety, systems toxicology.
Язык: Английский
Процитировано
0Marine Pollution Bulletin, Год журнала: 2025, Номер 215, С. 117870 - 117870
Опубликована: Март 28, 2025
Язык: Английский
Процитировано
0Journal of Hazardous Materials, Год журнала: 2025, Номер 493, С. 138312 - 138312
Опубликована: Апрель 18, 2025
Язык: Английский
Процитировано
0Analytical Chemistry, Год журнала: 2024, Номер unknown
Опубликована: Сен. 15, 2024
Sample preparation is an inevitable step in the screening workflow for identification of unknown pollutants aquatic environment. However, possible loss during sample has aroused serious concern but remains not effectively resolved. This study shows that high-risk omitted solid-phase extraction (SPE) can be identified via situ thin-film microextraction (TFME) coupled with high-resolution mass spectrometry. It was observed a total 541 features showed higher spectrometry signal intensity by using TFME comparison SPE. Subsequently, 28 compounds were from comparing recorded tandem spectra online database and validating standards. Notably, six out these completely SPE, including dye, drug, industrial product. confirmed lower efficiencies SPE attributed to limited volumes, losses transportation storage, entrapment columns. demonstrates should used as supplementary technique extending coverage workflows.
Язык: Английский
Процитировано
1Applied Sciences, Год журнала: 2024, Номер 14(19), С. 8645 - 8645
Опубликована: Сен. 25, 2024
The growing prevalence of pharmaceutical compounds in the environment raises significant concerns due to their potential impacts on ecological and human health. This present manuscript focuses methods used extract determine these pharmaceuticals water samples. It provides a comprehensive analysis extraction techniques analytical approaches employed for identification quantification environmental water. Due chemical properties widespread use, persist contaminate bodies, soil, sediments. presence aquatic has been linked several adverse effects organisms, including disruption physiological processes reproductive impairment. Furthermore, can affect health through food drinking contamination contribute antibiotic resistance. contaminants samples presents challenges complex matrix low concentrations target substances. Various sample preparation protocols, solid-phase (more than 76% studied literature) QuEChERS (quick, easy, cheap, effective, rugged, safe), coupled with liquid chromatography–tandem-mass spectrometry, are commonly determination. These offer high sensitivity, selectivity, efficiency identifying quantifying is, therefore, essential that ongoing research is conducted order develop more efficient mitigation strategies address effectively. also crucial increased awareness regulatory measures put place minimize risks associated pollutants.
Язык: Английский
Процитировано
0Analytica Chimica Acta, Год журнала: 2024, Номер 1335, С. 343456 - 343456
Опубликована: Ноя. 21, 2024
Язык: Английский
Процитировано
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