21 results match your criteria: "Institute for Analytical Research[Affiliation]"

Objectives: Bile acid diarrhea is a common but underdiagnosed condition. Because the gold standard test (SeHCAT) is time-consuming and not widely available, fecal bile acid excretion is typically assessed by chromatography and mass spectrometry. Although enzymatic cycling assays are well established for the rapid and cost-effective analysis of total bile acids (TBA) in serum or plasma, their full potential has yet not been extended to stool samples in clinical routine.

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Oxidative purification of microplastics in riverine suspended matter samples - Solving the challenge of plant debris removal for microplastic analysis.

Sci Total Environ

January 2025

Department of Environmental Analytical Chemistry, Helmholtz Centre for Environmental Research UFZ, Permoserstrasse 15, 04318 Leipzig, Germany; Institute of Analytical Chemistry, University of Leipzig, Linnéstraße 3, 04103 Leipzig, Germany. Electronic address:

Riverine suspended matter (river-SPM) contains large amounts of natural particles consisting of cellulose and lignin, posing a challenge for microplastic (MPs) analysis. Additionally, organic matter composition under seasonal and discharge-related dynamics varies for each river. Therefore, this study attempted to identify a universally applicable clean-up procedure to remove matrix particles with high organic matter content, mainly plant debris, from the river-SPM samples.

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Objectives: Serum total bile acid (TBA) levels are frequently assessed in clinical routine for the early detection of hepatobiliary dysfunction. However, the comparability of current 5th-generation TBA cycle assays based on 3α-hydroxysteroid dehydrogenase (3α-HSD) and their ability to quantify individual bile acids has not been systematically addressed.

Methods: Patient serum samples (n=60) across the diagnostically relevant TBA range (1-200 μmol/L) were analyzed using five TBA routine assays from Abbott, DiaSys, Diazyme, Beijing Strong (BSBE) and Randox on the same analyzer (BioMajesty JCA-BM6010/C).

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Quantification Approaches in Non-Target LC/ESI/HRMS Analysis: An Interlaboratory Comparison.

Anal Chem

October 2024

Department of Materials and Environmental Chemistry, Stockholm University, Svante Arrhenius väg 16, 11418 Stockholm, Sweden.

Nontargeted screening (NTS) utilizing liquid chromatography electrospray ionization high-resolution mass spectrometry (LC/ESI/HRMS) is increasingly used to identify environmental contaminants. Major differences in the ionization efficiency of compounds in ESI/HRMS result in widely varying responses and complicate quantitative analysis. Despite an increasing number of methods for quantification without authentic standards in NTS, the approaches are evaluated on limited and diverse data sets with varying chemical coverage collected on different instruments, complicating an unbiased comparison.

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To gain better understanding of how the transition to electric vehicles affects road dust (RD) composition, and potential health and environmental risks, it is crucial to analyze the chemical composition of RD and identify its sources. Sources of RD include wear of tire tread (TT), brake wear (BW) and road wear (RW). A relevant component of RD are tire and road wear particles (TRWPs).

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Article Synopsis
  • Proposed global regulations on PFAS have spurred research into safer alternative chemicals, leading to the investigation of two novel prototype PFAS designed for better environmental outcomes.
  • The study examined the in vitro metabolism of these prototypes in both human and rat liver fractions, revealing the production of primary metabolites like alcohols and carboxylic acids, but not complete mineralization.
  • Results indicated that rat liver enzymes metabolized the prototypes more efficiently than human liver enzymes, supporting the need for further research on the metabolic pathways and environmental impact of these alternative PFAS.
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Article Synopsis
  • Scientists from different fields are working together to solve the problem of plastic pollution, especially Early Career Researchers (ECRs).
  • ECRs need strong communication and project management skills to connect with various groups like industries, governments, and the public.
  • Advisors play a crucial role in helping ECRs grow and become successful scientists who can tackle the challenges of plastic pollution on a global scale.
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In this study the environmental fate of two novel trifluoromethoxy-substituted surfactants with respectively an ether or thioether linkage were investigated, of which the design aimed for less persistency and complete mineralization. Long-term microbial transformation studies under aerobic conditions in activated sludge-wastewater medium were performed for 126 days. A semi-closed experimental system with a trapping sorbent was selected to avoid losses of possible volatile transformation products (TPs).

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Forever legacies? Profiling historical PFAS contamination and current influence on groundwater used for drinking water.

Sci Total Environ

September 2023

Institute for Biodiversity and Ecosystem Dynamics, University of Amsterdam, Science Park 904, 1098 XH, Amsterdam, the Netherlands.

A wide range of PFAS residues were studied in an aquifer used for drinking water production which was affected by historical PFAS contamination from a landfill and military camp. Samples were taken at three monitoring and four pumping wells at different depths ranging from 33 to 147 m below the land surface and analysed for a series of 53 PFAS (C2-C14) and PFAS precursors (C4-C24). A comparison of results to earlier research from 2013, with a more limited range of PFAS, showed decreasing concentrations and migration of PFAS with increasing depth and distance from the contamination source.

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Current treatment options for organic waste contaminated with per- and polyfluoroalkyl substances (PFAS) are generally limited to incineration, composting or landfilling, all resulting in emissions. Dry pyrolysis is a promising emerging alternative to these practices, but there is uncertainty related to the fate of PFAS during this process. The present work first developed a robust method for the determination of PFAS in complex matrices, such as sewage sludge and biochar.

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Water-soluble polymers (WSPs) like polyethylene oxide (PEO) have annual production volumes ranging from thousands to millions of tonnes and are used in a wide variety of applications that enable a release into the aquatic environment. Despite these facts, a lack of quantitative trace-analytical methods for WSPs prevents the comprehensive study of their environmental occurrence. Here, size exclusion chromatography was hyphenated with electrospray ionization high-resolution mass spectrometry.

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Since their first appearance in 2008, synthetic cannabinoid receptor agonists (SCRAs) remain the most popular new psychoactive substances (NPS) in the EU. Following consumption, these drugs and their metabolites are urinary excreted and enter the sewage system enabling the application of wastewater-based epidemiology (WBE). Knowing the fate of target analytes in sewage water is essential for successful application of WBE.

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For analysis of microplastic (MP) particles in aquatic or solid compartments, standardized methods are required, yet data obtained by current methods are of limited comparability. Current methods include Fourier-transform Infrared (FT-IR) microscopy, Raman microscopy or thermo-analytical methods and attempts to compare data-sets from these methods have largely failed. Only little quality data based on validated methods and appropriate quality standards is available.

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The release of persistent and mobile organic chemicals (PMOCs) into the aquatic environment puts the quality of water resources at risk. PMOCs are challenging to analyze in water samples, due to their high polarity. The aim of this study was to develop novel analytical methods for PMOCs and to investigate their occurrence in surface and groundwater samples.

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In this study we have experimentally assessed different physicochemical parameters such as the distribution constant between octanol - water and between water and sludge for three perfluoroakyl substances (PFASs) widely used in waxes and coating materials: perfluorohexane (PFHxPA), perfluorooctane (PFOPA) and perfluorodecane (PFDPA) phosphonic acids. Distribution coefficients were assessed based on the procedures described in the OECD guideline 123 for partition coefficients while the studies of adsorption-desorption in sludge based on the indirect method of the OECD guideline 106. Besides, the removal behaviour of selected compounds has been evaluated using the green algae Desmodesmus subspicatus and microorganisms present in an effluent wastewater.

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Volatile per- and polyfluoroalkyl substances (PFASs) are often used as precursors in the synthesis of nonvolatile PFASs. The volatile PFASs, which include the perfluoroalkyl iodides (PFAIs), fluorotelomer iodides (FTIs), fluorotelomer alcohols (FTOHs), fluorotelomer olefins (FTOs), fluorotelomer acrylates (FTACs), and fluorotelomer methacrylates (FTMACs), are often produced starting from the telomerization process. These volatile compounds can be present in the air and water environment and can be transformed into highly persistent perfluoroalkyl carboxylic acids.

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Mind the Gap: Persistent and Mobile Organic Compounds-Water Contaminants That Slip Through.

Environ Sci Technol

October 2016

Institute for Biodiversity and Ecosystem Dynamics, University of Amsterdam, Science Park 904, 1098 XH Amsterdam, The Netherlands.

The discharge of persistent and mobile organic chemicals (PMOCs) into the aquatic environment is a threat to the quality of our water resources. PMOCs are highly polar (mobile in water) and can pass through wastewater treatment plants, subsurface environments and potentially also drinking water treatment processes. While a few such compounds are known, we infer that their number is actually much larger.

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Characterization of 3-Aminopropyl Oligosilsesquioxane.

Anal Chem

May 2016

Institute for Analytical Research, Hochschule Fresenius Limburger Strasse 2, 65510 Idstein, Germany.

The synthesis routes in the production of polysilsesquioxanes have largely relied upon in situ formations. This perspective often leads to polymers in which their basic structures including molecular weight and functionality are unknown [ Lichtenhan , J. D.

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High Resolution Mass Spectrometry of Polyfluorinated Polyether-Based Formulation.

J Am Soc Mass Spectrom

February 2016

Institute for Biodiversity and Ecosystem Dynamics, University of Amsterdam, Science Park 904, Amsterdam, 1098XH, The Netherlands.

High resolution mass spectrometry (HRMS) was successfully applied to elucidate the structure of a polyfluorinated polyether (PFPE)-based formulation. The mass spectrum generated from direct injection into the MS was examined by identifying the different repeating units manually and with the aid of an instrument data processor. Highly accurate mass spectral data enabled the calculation of higher-order mass defects.

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The combined effects of degree of deacetylation (DD) and degree of polymerization (DP) on the ability of chitosan to interact with olive oil was studied. The oil-binding test, a method that makes use of olive oil as a representative fat, was adopted as a measure of the interaction of chitosan and olive oil. The oil-binding capacities of twelve chitosan samples with DPs ranging from 470 to 1450 and DDs of 75% to 95% were determined.

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Polyethoxylated 2-perfluoroalkylethanols ('fluorotelomer ethoxylates', F-(CF(2)-CF(2)-)(x)-(CH(2)-CH(2)-O)(y)-H, FTEO) are an important class of non-ionic fluorinated surfactants, which have been disregarded as potential source of per- and polyfluorinated organic pollutants despite their high production and application amounts. A commercial mixture of FTEO with a perfluoroalkyl chain length between 6 and 10 carbon atoms and an ethoxymer distribution between 0 and 13 was subjected to a biodegradation test. Monitoring of the aerobic biotransformation process by HPLC-ESI-MS/MS showed that FTEO are rapidly transformed with a half-life of approximately 1d.

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