TY - JOUR A1 - Tjaden, B. A1 - Baum, K. A1 - Marquardt, V. A1 - Simon, M. A1 - Trajkovic-Arsic, M. A1 - Kouril, T. A1 - Siebers, B. A1 - Lisec, Jan A1 - Siveke, J. T. A1 - Schulte, J. H. A1 - Benary, U. A1 - Remke, M. A1 - Wolf, J. A1 - Schramm, A. T1 - MYCN-induced metabolic rewiring creates novel therapeutic vulnerabilities in neuroblastoma N2 - MYCN is a transcription factor that is aberrantly expressed in many tumor types and is often correlated with poor patient prognosis. Recently, several lines of evidence pointed to the fact that oncogenic activation of MYC family proteins is concomitant with reprogramming of tumor cells to cope with an enhanced need for metabolites during cell growth. These adaptions are driven by the ability of MYC proteins to act as transcriptional amplifiers in a tissue-of-origin specific manner. Here, we describe the effects of MYCN overexpression on metabolic reprogramming in neuroblastoma cells. Ectopic expression of MYCN induced a glycolytic switch that was concomitant with enhanced sensitivity towards 2-deoxyglucose, an inhibitor of glycolysis. Moreover, global metabolic profiling revealed extensive alterations in the cellular metabolome resulting from overexpression of MYCN. Limited supply with either of the two main carbon sources, glucose or glutamine, resulted in distinct shifts in steady-state metabolite levels and significant changes in glutathione metabolism. Interestingly, interference with glutamine-glutamate conversion preferentially blocked proliferation of MYCN overexpressing cells, when glutamine levels were reduced. Thus, our study uncovered MYCN induction and nutrient levels as important metabolic master switches in neuroblastoma cells and identified critical nodes that restrict tumor cell proliferation. KW - Mass-spectrometry KW - Tumor metabolism KW - MYCN PY - 2018 DO - https://doi.org/10.1101/423756 SP - 1 EP - 21 PB - Cold Spring Harbor Laboratory CY - Cold Spring Harbor, NY AN - OPUS4-46815 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Kienle, L. A1 - Duppel, V. A1 - Mogwitz, B. A1 - Janek, J. A1 - Kreutzbruck, Marc A1 - Leineweber, A. A1 - Simon, A. T1 - Synthesis - real structure - property: the showcase of silver-rich Ag2Se N2 - The structures and properties of silver selenide samples strongly depend on the method of preparation. Thin films prepared by pulsed laser deposition (PLD) contain lamellae of two low-temperature modifications of Ag2Se whose structures were analyzed in detail by electron microscopy techniques. Besides the stable and known Naumannite-type phase (LT1), a metastable phase was observed (LT2), and the phase transformation was examined in situ. Via cooling and annealing, LT2 becomes dominant in thin films, thus enabling solving the structure of LT2 by electron diffraction. These experiments and HRTEM point to an Acanthite-type (stable low-temperature modification of Ag2S) structure of LT2. Rapid-quenching procedures were applied for the first synthesis of LT2 as bulk sample. Depending on the conditions of melt spinning experiments, well-defined products were formed. In one series, we found a separation of LT1 and LT2 into distinct morphologies, i.e. microspheres and dendrites, respectively. The results on the magnetoresistance of the rapidly quenched materials support previous work. PY - 2011 DO - https://doi.org/10.1021/cg200167j SN - 1528-7483 VL - 11 IS - 6 SP - 2412 EP - 2421 PB - American Chemical Society CY - Washington, DC, USA AN - OPUS4-25388 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Kienle, L. A1 - Duppel, V. A1 - Lembke, G. A1 - Mogwitz, B. A1 - Janek, J. A1 - Kreutzbruck, Marc A1 - Simon, A. T1 - Microstructure and magnetoresistance of heterogeneous gold-rich Ag3Au1.1Te2 N2 - Dispersions of very small non-magnetic metal particles or inclusions in a non-magnetic semiconductor matrix are well known to produce unusually large and linear magnetoresistance effects. So far these materials were limited to the binary silver-rich chalcogenides Ag2Se and Ag2Te. In this contribution Ag3AuTe2 was selected as a first candidate for a ternary matrix material, thus offering enhanced capabilities for the generation of heterogeneous microstructure and spatially varying composition on the nanoscale. In gold-rich Ag3Au1.1Te2 two kinds of inhomogeneities are present, namely Au deposits with a size on the micron scale and an inhomogeneous distribution of Au and Ag within the matrix. The matrix consists of micron-sized grains with the structure type of Ag3AuTe2 as studied by electron microscopy. Like the binary silver chalcogenide phases, the material also shows a large and linear magnetoresistance effect. The transversal magnetoresistance effect was measured between 20 K and 270 K in magnetic fields up to B = 5 T. The results are discussed on the basis of existing models for a large and linear positive MR effect. KW - Petzite KW - Magnetosensor KW - Electron microscopy KW - Nonstoichiometry KW - Magnetoresistance PY - 2010 DO - https://doi.org/10.1016/j.solidstatesciences.2010.07.029 SN - 1293-2558 SN - 1873-3085 VL - 12 IS - 10 SP - 1770 EP - 1778 PB - Elsevier CY - Amsterdam AN - OPUS4-22281 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Blüml, P. A1 - Hosp, E. A1 - Ritter, R. A1 - Simon, B. T1 - Optische Verfahren in der experimentellen Spannungsanalyse PY - 1982 SN - 0083-5560 IS - 439 SP - 97 EP - 121 PB - VDI-Verl. CY - Düsseldorf AN - OPUS4-36387 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Knechtel, Sophie A1 - Schmidt, Simon A1 - Mishra, K. B. A1 - Wehrstedt, Klaus-Dieter T1 - Modellierung der Hauptbrandszenarien von flüssigem Wasserstoff (LH2) mittels CFD N2 - Die sichere Lagerung und der Transport von Flüssigwasserstoff (LH2) verlangen nach verlässlichen Abschätzungen möglicher Risiken durch Feuer oder Explosion. Aufgrund des breiten Explosionsbereichs (4 Vol.-% - 74 Vol.-%) reagiert Wasserstoff sehr schnell und produziert hohe Flammentemperaturen. Da Wasserstoffflammen ruß- bzw. farblos sind, ist Wärmestrahlung im Fernfeld kein Risikofaktor. Allerdings stellen die hohe lokale Wärmestrahlung und die nicht sichtbaren Flammen eine Gefahr für Menschen und Infrastruktur in der Nähe dar. Es ist daher notwendig die Gefahren von LH2-Feuern sorgfältig zu bewerten. Einerseits sind experimentelle Untersuchungen verschiedener Szenarien teuer, andererseits können sie teilweise auch praktisch nicht durchführbar sein. Numerische Simulationen dieser Szenarien können ein Ausweg aus diesem Problem sein. In der vorliegenden Arbeit wird ein solcher Ansatz genutzt, um große Brandszenarien mit LH2 mittels CFD (Computational Fluid Dynamics) zu modellieren und so die notwendigen Sicherheitsabstände abzuschätzen. Der Fokus liegt dabei auf der Simulation von Jet- und Pool-Feuerszenarien mit einem kommerziellen CFD-Code (Ansys CFX). Die benötigten geometrischen Modelle werden für Jet- und Pool-Feuer erstellt und mit den nötigen Randbedingungen implementiert. Wichtige Submodelle für chemische Reaktionen (Einschritt- und detaillierte Modelle), Verbrennung (Eddy-Dissipation- und Flamelet-Modell) und Strahlung (Discrete-Transfer-Modell) werden genutzt. Die maximal simulierten Flammentemperaturen liegen bei ~2100 K für Jet-Feuer und ~2300 K für Pool-Feuer. Um Aussagen zu thermischen Sicherheitsabständen zu treffen, wurden die Spezifischen Ausstrahlungen (SEP) ermittelt und anschließend entsprechende Positionsfaktoren gewählt, um verlässliche Sicherheitsabstände zu berechnen. Je nach Bedarf können CFD-Modelle sowohl für qualitative als auch für quantitative Risikobewertungen von LH2-Großbränden genutzt werden. T2 - 12. Fachtagung Anlagen-, Arbeits- und Umweltsicherheit CY - Köthen, Germany DA - 05.11.2015 KW - Flüssigwasserstoff KW - Großbrand KW - Poolfeuer KW - Jet-Feuer KW - CFD KW - Sicherheitsabstand PY - 2015 SN - 978-3-86011-091-1 SP - Paper P-11, 1 EP - 8 AN - OPUS4-34827 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Hoesl, Simone A1 - Neumann, B. A1 - Techritz, Sandra A1 - Sauter, G. A1 - Simon, R. A1 - Schlüter, H. A1 - Linscheid, M. W. A1 - Theruing, F. A1 - Müller, Larissa A1 - Jakubowski, Norbert T1 - Internal standardization of LA-ICP-MS immunoimaging via printing of universal metal spiked inks onto tissue sections N2 - Formalin-fixed paraffin-embedded (FFPE) specimen from biopsy materials are a widespread sample format for pathologists and medical researchers. Pathologists are archiving vast numbers of FFPE samples which can be stored for decades. Conventional immunohistochemical staining (IHC) of biomarkers on FFPE tissue sections is one of the most important analytical techniques for cancer diagnosis and pathology in general. However standardization for IHC samples and quality management is tedious and differs significantly from clinic to clinic. Combining established IHC staining strategies with modern mass spectrometry mediated methods would increase it`s potential and enable access of large FFPE archives for multiplexed quantitation purposes. In this work element mass spectrometry and a new ink-jet printed internal standardization approach was successfully combined with IHC staining to facilitate quantitative multiplex assays for archived FFPE samples. The printing strategy improves elemental image resolution and reproducibility of paraffin embedded breast cancer tissue sections in laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS) using conventional IHC staining as a model system to investigate the new capabilities of this technique. For the internal standardization we applied a conventional CD-ink-jet printer to print a metal spiked ink onto the top of thin layer tissue sections with constant density. Printing was carried out in a direct comparison to an iodination of the tissue section as previously described as an alternative standardization method. The use of the printed internal standard allowed correction of the fluctuation during the laser ablation process and compensated instrumental drift effects. Mediated by the ink correction approach we achieved better signal-to-background-ratios (SBR) of 74 and better spatial resolution of 30 µm compared to iodination (SBR=23). This improved performance was demonstrated on tumorous areas in FFPE breast cancer tissue sections and allowing detection of Her-2 in tumorous areas of this tissue with significantly improved contrast. KW - Internal standardization KW - LA-ICP-MS KW - Immuno imaging PY - 2016 DO - https://doi.org/10.1039/c5ja00409h SN - 0267-9477 SN - 1364-5544 VL - 31 IS - 3 SP - 801 EP - 808 AN - OPUS4-35711 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Gili, A. A1 - Bischoff, B. A1 - Simon, U. A1 - Schmidt, Franziska A1 - Kober, D. A1 - Görke, O. A1 - Bekheet, M. A1 - Gurlo, A. T1 - Ceria-based dual-phase membranes for high-temperature Carbon dioxide separation: Effect of iron doping and pore generation with MgO template N2 - Dual-phase membranes for high-temperature carbon dioxide Separation have emerged as promising technology to mitigate anthropogenic greenhouse gases emissions, especially as a pre- and post-combustion separation technique in coal burning power plants. To implement These membranes industrially, the carbon dioxide permeability must be improved. In this study, Ce_(0.8) Sm_(0.2) O_(2-d) (SDC) and Ce_(0.8)Sm_(0.19)Fe_(0.01)O_(2-d) (FSDC) ceramic powders were used to form the skeleton in dual-Phase membranes. The use of MgO as an environmentally friendly pore generator allows control over the membrane porosity and microstructure in order to compare the effect of the membrane’s ceramic phase. The ceramic powders and the resulting membranes were characterized using ICP-OES, HSM, gravimetric analysis, SEM/EDX, and XRD, and the carbon dioxide flux density was quantified using a high-temperature membrane permeation setup. The carbon dioxide permeability slightly increases with the addition of iron in the FSDC membranes compared to the SDC membranes mainly due to the reported scavenging effect of iron with the siliceous impurities, with an additional potential contribution of an increased crystallite size due to viscous flow sintering. The increased permeability of the FSDC system and the proper microstructure control by MgO can be further extended to optimize carbon dioxide permeability in this membrane system. KW - Samarium doped ceria KW - SDC KW - FSDC KW - CO2 separation membranes KW - Scavenging effect of iron KW - Permeability PY - 2019 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-488612 DO - https://doi.org/10.3390/membranes9090108 SN - 2077-0375 VL - 9 IS - 9 SP - 108, 1 EP - 15 PB - MDPI AN - OPUS4-48861 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - RPRT A1 - Brandes, E. A1 - Colson, B. A1 - Frost, K. A1 - Lüth, Peter A1 - Simon, K. A1 - Stolz, T. A1 - Uhlig, S. T1 - Evaluation of the interlaboratory test 2015 – 2016 on the method UN Test L.2 “Sustained combustibility test” / EN ISO 9038:2013 “Determination of sustained combustibility of liquids" N2 - The test methods UN Test L.2 / EN ISO 9038:2013 DIN EN 15188:2007 are applied to characterize the sustained combustibility of liquids i.e. the behaviour of a material under specified test conditions, whereby its vapour can be ignited by an ignition source and sufficient flammable vapour is produced to continue burning for at least 15 s after the source of ignition has been removed. The aims of this interlaboratory test (IT) are the verification and/or the improvement (if necessary) of the verification data (reference material) in Annex B of EN ISO 9038:2013, the assessment of influencing (disturbing) factors (laboratory specific factors, which possibly may have an influence on the test result) and the assessment of the performance of the participating laboratories. It could be demonstrated that the reference materials n-Dodecane, n-Decane and n-Undecane as mentioned in the standard are suitable and the verification shall continue to be valid. Sustained combustibility tests are influenced by several factors like the presence of a draught shield, the experience of the laboratory assistant, verification of the apparatus, calibration of the metering device. Based on the interlaboratory test, the gained experience and the actual results, well-founded measures / actions can be recommended to improve execution of the method. The IT was organized by PTB, BAM and QuoData GmbH in the framework of the co-operation project CEQAT-DGHS Centre for Quality Assurance for Testing of Dangerous Goods and Hazardous Substances. KW - Dangerous goods KW - Hazardous substances KW - Test method KW - Quality assurance KW - Interlaboratory comparison KW - Round robin test KW - Validation KW - Sustained combustibility KW - Reference material KW - Gefahrgut KW - Gefahrstoff KW - Prüfmethode KW - Qualitätssicherung KW - Ringversuch KW - Validierung KW - Selbstunterhaltende Verbrennung KW - Referenzmaterial PY - 2017 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-410270 SN - 978-3-9818270-3-3 SP - 1 EP - 103 PB - Bundesanstalt für Materialforschung und -prüfung (BAM) CY - Berlin AN - OPUS4-41027 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Simon, Fabian A1 - Gehrenkemper, Lennart A1 - Dierckes, G. A1 - Göckener, B. A1 - Koschorreck, J. A1 - Meermann, Björn T1 - Analyse von PFAS mittels (Non-)Target HRMS, dTOPA und EOF in Schwebstoff-Proben aus Zeitreihen der Umweltprobenbank N2 - Per- und polyfluorierte Alkylverbindungen (PFAS) sind eine Substanzklasse bestehend aus mehreren tausenden Einzelverbindungen. Unter PFAS zählen alle Verbindungen, die mindestens eine perfluorierte Methyl- (-CF3) oder Methylen-Gruppe (-CF2-) besitzen. Somit zählt auch ein großer Teil der fluorierten Medikamente, Pflanzenschutzmittel oder Biozide in die PFAS-Substanzklasse. Aufgrund der Persistenz, Bioakkumulation in Nahrungsketten, Toxizität und der ubiquitären Verbreitung von PFAS zählen sie zu den „emerging pollutants“. Die PFAS-Analytik ist wegen ihrer vielfältigen physikalisch-chemischen Eigenschaften und der sehr hohen Anzahl an PFAS eine große Herausforderung. Da es für viele Anwendungen noch ungewiss ist, welche PFAS verwendet werden, wie sie in die Umwelt gelangen und welche Transformations- bzw. Abbauprodukte entstehen, stoßen analytische Ansätze, die nur auf Einzelsubstanzen abzielen, hier an ihre Grenzen. PFAS-Summenparameter-Methoden, die darauf abzielen ein möglichst vollständiges Abbild der PFAS-Belastungssituation widerzuspiegeln, werden daher immer wichtiger. KW - PFAS KW - HR-CS-GFMAS KW - Fluorine KW - SPM KW - LC-MS/MS KW - Schwebstoffe PY - 2023 VL - 5 SP - 1 EP - 6 AN - OPUS4-57544 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Zweigle, J. A1 - Capitain, C. A1 - Simon, Fabian Michael A1 - Roesch, Philipp A1 - Bugsel, B. A1 - Zwiener, C. T1 - Non-extractable PFAS in functional textiles − Characterization by complementary methods: oxidation, hydrolysis, and fluorine sum parameters N2 - Per- and polyfluoroalkyl substances (PFAS) are widely used for durable water-repellent finishing of different fabrics and textiles like outdoor clothing, carpets, medical textiles and more. Existing PFAS extraction techniques followed by target analysis are often insufficient in detecting widely used side-chain fluorinated polymers (SFPs) that are barely or non-extractable. SFPs are typically copolymers consisting of a non-fluorinated backbone with perfluoroalkyl side-chains to obtain desired properties. We compared the accessible analytical information and performance of complementary techniques based on oxidation (dTOP assay, PhotoTOP), hydrolysis (THP assay), standard extraction, extractable organic fluorine (EOF), and total fluorine (TF) with five functional textiles and characterized 7 further textiles only by PhotoTOP oxidation. The results show that when applied directly to textile samples, oxidation by dTOP and PhotoTOP and also hydrolysis by the THP are able to capture large fractions of the TF in form of perfluoroalkyl side-chains present in the textiles while methods relying on extracts (EOF, target and non-target analysis) were much lower (e.g., factor ~25-50 lower). The conversion of large fractions of the measured TF into PFCAs or FTOHs from fluorinated side chains is in contrast to previous studies. Concentrations ranged from