TY - JOUR A1 - Pauli, Jutta A1 - Pochstein, Marieke A1 - Haase, A. A1 - Napp, J. A1 - Luch, A. A1 - Resch-Genger, Ute T1 - Influence of label and charge density on the association of the therapeutic monoclonal antibodies trastuzumab and cetuximab conjugated to anionic fluorophores N2 - The design of bright and functional dye–protein conjugates requires hydrophilic and stable fluorophores with high molar absorption coefficients and high fluorescence quantum yields,which must not be prone to dimerization, as well as conservation of protein function and suppression of protein association. Although many synthetic dyes meet these needs, the influence of dye charge on bioconjugate performance is commonly neglected. This encouraged us to assess the spectroscopic properties, antibody functionality, binding behavior, folding, and association of conjugates of the therapeutic antibodies trastuzumab and cetuximab with the red cyanine dyes S0586, S2381,and 6SIDCC (bearing two, three, and six sulfonate Groups respectively. Our results demonstrate a negligible effect of dye labeling on antibody folding, yet a strong influence of Label charge and density on antibody isoelectric points and association.Especially 6SIDCC decreased strongly the isoelectric points of both antibodies and their heavy or light chains even at low labeling degrees, thus favoring protein association. Although an increasingly negative dye charge reduces Antigen affinity as shown in a competitive immunoassay, all conjugates still bound to cells overexpressing the target of the respective antibody. Obviously, dyes that cause minimum dimerization with a small number of charged groups are best for conjugate brightness, minimum protein association, and strong target binding. This underlines the need to consider dye Charge for the rational design of conjugates with Optimum performance. KW - Fluorophore KW - Antibody KW - 2D gel electrophoresis KW - Isoelectric point KW - Protein association PY - 2016 DO - https://doi.org/10.1002/cbic.201600299 SN - 1439-7633 SN - 1439-4227 VL - 18 IS - 1 SP - 101 EP - 110 PB - WILEY-VCH Verlag GmbH & Co. KGaA CY - Weinheim AN - OPUS4-38573 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Pauli, Jutta T1 - Evaluierung neuer Fluoreszenzfarbstoffe für die in-vivo-Diagnostik T2 - 88. Deutscher Röntgenkongress CY - Berlin, Germany DA - 2007-05-16 PY - 2007 AN - OPUS4-13877 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Pauli, Jutta T1 - Characterization of a new near infrared dyes for molecular imaging T2 - Method and Application of Fluerescence (MAF10) CY - Salzburg, Austria DA - 2007-09-09 PY - 2007 AN - OPUS4-16407 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Pauli, Jutta T1 - Entwicklung von Fluoreszenzquantenausbeutestandards N2 - Lumineszenzmethoden und funktionelle Chromophore erlangten in den letzten Jahren breite Anwendungen in den Material- und Lebenswissenschaften wie z.B. in der medizinischen Diagnostik, der Beleuchtungs- und Displaytechnologie, der Photovoltaik oder im Sicherheitsbereich für die Echtheitskodierung. Entscheidend für eine hohe Effizienz und Nachweisempfindlichkeit funktioneller Chromophore ist eine große Helligkeit bzw. Brillanz. Brillante Stoffe zeichnen sich durch eine hohe Absorption des anregenden Lichtes (messbar über den molaren Extinktionskoeffizienten) aus sowie durch eine effiziente Umwandlung des absorbierten Lichtes in Lumineszenzlicht bzw. durch eine große Photolumineszenzquantenausbeute aus. Die Bestimmung der Schlüsselgröße Fluoreszenzquantenausbeute erfolgt i.a. relativ zu einem Farbstoff bekannter Fluoreszenzquantenausbeute über einen Vergleich der absorptionsgewichteten integralen Fluoreszenzspektren von Probe und Standard. Hierfür werden Referenzmaterialien mit zertifizierten Fluoreszenzquantenausbeuten benötigt, die bislang nicht verfügbar sind. Im folgenden werden die laufenden Forschungsarbeiten an einer Serie an Fluoreszenzquantenausbeutestandard vorgestellt, die im Spektralbereich von 350 nm – 1050 nm emittieren. Diese Materialien können auch zur Überprüfung von Ulbrichtkugelmessplätzen eingesetzt werden. T2 - Colloquium Optical Spectrometry (COSP) CY - Berlin, Germany DA - 27.11.2017 KW - Fluoreszenz KW - Referenzmaterial KW - Quantenausbeute PY - 2017 AN - OPUS4-44095 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Pauli, Jutta T1 - Influence of the Dimerization of Fluorescent Dyes on the Spectroscopic Properties of their lgG Conjugates T2 - Molekulare Bildgebung 10 (MOBI10) CY - Seeon-Seebruck, Germany DA - 2010-11-04 PY - 2010 AN - OPUS4-22661 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Pauli, Jutta T1 - Bright Functional Herceptin Conjugates with a Remarkably High Number of Fluorophores for Optical Imaging T2 - 5th EuCheMS CY - Istanbul, Turkey DA - 2014-08-31 PY - 2014 AN - OPUS4-31849 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Pauli, Jutta T1 - Design and characterization of a new contrast agent for the specific and sensitive detection of tumor via in vivo fluorescence imaging T2 - Method and Application of Fluerescence (MAF10) CY - Salzburg, Austria DA - 2007-09-09 PY - 2007 AN - OPUS4-16406 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Pauli, Jutta T1 - Analytical and Spctroscopic tools for the Design of Highly Flourescent Conjugates T2 - ANAKON 2013 CY - Essen, Germany DA - 2013-03-04 PY - 2013 AN - OPUS4-28471 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Pauli, Jutta T1 - Influence of biological systems on the intensity of the light emission of fluorophores T2 - Molekulare Bildgebung CY - Kiel, Germany DA - 2007-07-05 PY - 2007 AN - OPUS4-16404 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Pauli, Jutta T1 - Spectroscopic properties of new near infrared dyes for molecular imaging T2 - Molekulare Bildgebung CY - Kiel, Germany DA - 2007-07-05 PY - 2007 AN - OPUS4-16405 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Mathejczyk, J.E. A1 - Pauli, Jutta A1 - Dullin, C. A1 - Resch-Genger, Ute A1 - Alves, F. A1 - Napp, J. T1 - High-sensitivity detection of breast tumors in vivo by use of a pH-sensitive near-infrared flurorescence probe N2 - We investigated the potential of the pH-sensitive dye, CypHer5E, conjugated to Herceptin (pH-Her) for the sensitive detection of breast tumors in mice using noninvasive time-domain near-infrared fluorescence imaging and different methods of data analysis. First, the fluorescence properties of pH-Her were analyzed as function of pH and/or dye-to-protein ratio, and binding specificity was confirmed in cell-based assays. Subsequently, the performance of pH-Her in nude mice bearing orthotopic HER2-positive (KPL-4) and HER2-negative (MDA-MB-231) breast carcinoma xenografts was compared to that of an always-on fluorescent conjugate Alexa Fluor 647-Herceptin (Alexa-Her). Subtraction of autofluorescence and lifetime (LT)-gated image analyses were performed for background fluorescence suppression. In mice bearing HER2-positive tumors, autofluorescence subtraction together with the selective fluorescence enhancement of pH-Her solely in the tumor's acidic environment provided high contrast-to-noise ratios (CNRs). This led to an improved sensitivity of tumor detection compared to Alexa-Her. In contrast, LT-gated imaging using LTs determined in model systems did not improve tumor-detection sensitivity in vivo for either probe. In conclusion, pH-Her is suitable for sensitive in vivo monitoring of HER2-expressing breast tumors with imaging in the intensity domain and represents a promising tool for detection of weak fluorescent signals deriving from small tumors or metastases. KW - Optical probe KW - pH sensing KW - Cyanine KW - In vivo near-infrared fluorescence imaging KW - Fluorescence lifetime imaging KW - Breast tumor monitoring KW - Herceptin PY - 2012 DO - https://doi.org/10.1117/1.JBO.17.7.076028 SN - 1083-3668 SN - 1560-2281 VL - 17 IS - 7 SP - 076028-1 - 076028-9 PB - SPIE CY - Bellingham, Wash. AN - OPUS4-26297 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Mota Gassó, Berta A1 - Schmidt, Wolfram A1 - Pauli, Jutta A1 - Sturm, Heinz T1 - Influences of hydration effects on the flow phenomena of concrete with admixtures N2 - Today, chemical admixtures like superplasticisers and stabilising agents are extremely important for modern concrete technology. These agents have meanwhile become common practice in concrete technology, but the understanding within the entire system lags far behind their application. The macroscopic rheology of concrete in the presence of superplasticizers strongly depends upon effects on a much smaller scale such as the hydration of the cement, the adsorption of superplasticizers, and the pore solution chemistry. T2 - 2nd International Conference on the Chemistry of Construction Materials CY - München, Germany DA - 10.10.2016 KW - Rheology KW - Cement KW - Superplasticiser PY - 2016 SN - 978-3-936028-96-6 VL - 50 SP - 276 EP - 279 PB - Gesellschaft Deutscher Chemiker e.V. CY - Frankfurt am Main AN - OPUS4-38849 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Ramirez Caro, Alejandra A1 - Pauli, Jutta A1 - Mota, Berta A1 - Crasselt, Claudia A1 - Artemeva, Elena A1 - Schmidt, Wolfram A1 - Resch-Genger, Ute T1 - A Spectroscopic Study of the Superplasticizer Effect on Early Cement Hydration N2 - Organic/inorganic mixtures were prepared from ordinary Portland cement (OPC), water (w/c 0.22), a fluorescent dye in aqueous solution (stable at alkaline pH; BAM-I), and two different comb shape polycarboxylates (PCEs), i.e., high charge (PCE-HC) and low charge (PCE-LC), respectively. Rheological and calorimetric measurements were performed prior to optical studies in order to select PCE concentrations. Absorption and fluorescence spectroscopy of the system OPC + BAM-I (CBAM-I) revealed maxima of dye BAM-I located at 645 nm and 663 nm, respectively. In presence of PCE-HC and PCE-LC, these mixtures displayed a small red shift in reflectance and a faster decrease in intensity compared to studies with CBAM-I; however, only slight differences were observed between the different PCEs. With time, all systems exhibited a decrease in intensity of BAM-I in absorption/reflectance and emission. This could be caused by dye adsorption and possibly decomposition when in contact with cement particles or hydration products. T2 - The Sixth International Symposium on Nanotechnology in Construction (NICOM6) CY - Hong Kong, China DA - 02.12.2018 KW - Cement KW - Optical Spectroscopy KW - Dye KW - Hydration PY - 2018 SP - 1 EP - 9 AN - OPUS4-49378 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Ramirez Caro, Alejandra A1 - Pauli, Jutta A1 - Schmidt, Wolfram A1 - Resch-Genger, Ute T1 - Study of the superplasticizer-cement hydration interaction by optical spectroscopy N2 - Nowadays, superplasticizers (SPs) are widely used to increase fluidity and reduce water content in concrete; thus, allowing better workability for final applications. The present study will focus on the hydration effect using comb shape polycarboxylates (PCEs), which are known to allow a very low water/cement ratio (w/c of 0.20) or less.Optical methods have been successfully used for the analysis and monitoring of the interactions between a broad variety of nanoscale and molecular systems like nanoparticles of various chemical composition and different types of organic ligands or biomolecules.This encouraged us to assess the potential of these methods, and particularly fluorescence, for the investigation of the interactions that occur at the interface between hydrate surfaces of cement particles and PCE at a very early stage of concrete formation and to differentiate between the impact of PCE’s molecular structures on such interactions. T2 - 2nd International Conference on the Chemistry of Construction Materials CY - Munich, Germany DA - 10.10.2016 KW - Cement KW - Dye KW - Superplasticizers KW - Fluorescence PY - 2016 SN - 978-3-936028-96-6 VL - 50 SP - 260 EP - 263 PB - Gesellschaft Deutscher Chemiker e.V. CY - Frankfurth am Main AN - OPUS4-38881 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Ramirez Caro, Alejandra A1 - Pauli, Jutta T1 - Study of the hydration of superplasticizer-cement pastes with optical spectroscopy N2 - Chemical admixtures like superplasticizers or stabilizing agents are of ever increasing importance for modern concrete technology. Although such admixtures have meanwhile become common practice in many applications of concrete technology, the understanding of these highly complex systems is still limited and the relevant parameters, which predominantly control the interaction between the superplasticizer and the cement components, have not been identified yet. Optical methods have been successfully used for the analysis and monitoring of the interactions between a broad variety of nanoscale and molecular systems like nanoparticles of various chemical composition and different types of organic ligands or biomolecules. This encouraged us to assess the potential of these methods, and particularly reflectance and fluorescence measurements, for the study of the interactions that occur at the interface between particle or hydrate surfaces and the fluid phase at a very early stage of concrete formation. Special emphasis is dedicated to search for and identify differences between commonly used superplasticizers. Here, we focus on hydration effects using commercial comb shape polycarboxylate ethers (PCEs) with different charge densities, which are known to allow a very low water/cement ratio (w/c of 0.20 or less) while maintaining good workability. Based upon changes of the intensity of the reflectance and fluorescence signal and spectral effects of a dye, acting as optical reporter, a model for the interactions of dye, PCE molecules and cement nanoparticles in the very first phase of cement hydration is derived T2 - Gesellschaft Deutscher Chemiker-Analytische Chemie-Anakon 2017 CY - Tübingen, Germany DA - 03.04.2017 KW - Cement hydration KW - Optical spectroscopy KW - Superplasticizers PY - 2017 AN - OPUS4-39882 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Ramirez Caro, Alejandra A1 - Pauli, Jutta T1 - Study of the superplasticizer-cement hydration interaction by optical spectroscopy N2 - Chemical admixtures like superplasticizers or stabilizing agents are of ever increasing importance for modern concrete technology. Although such admixtures have meanwhile become common practice in many applications of concrete technology, the understanding of these highly complex systems is still limited and the relevant parameters, which predominantly control the interaction between the superplasticizer and the cement components, have not been identified yet. Optical methods have been successfully used for the analysis and monitoring of the interactions between a broad variety of nanoscale and molecular systems like nanoparticles of various chemical composition and different types of organic ligands or biomolecules. This encouraged to assess the potential of these methods for the investigation of the interactions that occur at the interface between particle or hydrate surfaces and the fluid phase at a very early stage of concrete formation and to differentiate between different superplasticizer. T2 - 2. ICCCM CY - Munich, Germany DA - 10.10.2016 KW - Optical spectroscopy KW - Cement hydration PY - 2016 AN - OPUS4-38474 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Ramirez Caro, Alejandra A1 - Mota, Berta A1 - Artemeva, E. A1 - Pauli, Jutta A1 - Schmidt, Wolfram A1 - Resch-Genger, Ute T1 - A spectroscopic study of the superplasticizer effect on early cement hydration N2 - Organic/inorganic mixtures were prepared from ordinary Portland cement (OPC), water (w/c 0.22), a fluorescent dye in aqueous solution (stable at alkaline pH; BAM-I), and two different comb shape polycarboxylates (PCEs), i.e., high charge (PCE-HC) and low charge (PCE-LC), respectively. Rheological and calorimetric measurements were performed prior to optical studies in order to select PCE concentrations. Absorption and fluorescence spectroscopy of the system OPC + BAM-I (CBAM-I) revealed maxima of dye BAM-I located at 645 nm and 663 nm, respectively. In presence of PCE-HC and PCE-LC, these mixtures displayed a small red shift in reflectance and a faster decrease in intensity compared to studies with CBAM-I; however, only slight differences were observed between the different PCEs. With time, all systems exhibited a decrease in intensity of BAM-I in absorption/reflectance and emission. This could be caused by dye adsorption and possibly decomposition when in contact with cement particles or hydration products. T2 - 20. Internationale Baustofftagung CY - Weimar, Germany DA - 12.09.2018 KW - Optical spectroscopie KW - Cement hydration KW - Dyes PY - 2018 SN - 978-3-00-059950-7 VL - 20 SP - 1 EP - 6 PB - F.A. Finger-Institut für Baustoffkunde CY - Weimar AN - OPUS4-46277 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Ramirez Caro, Alejandra A1 - Pauli, Jutta A1 - Mota, Berta A1 - Simon, Sebastian A1 - Schmidt, Wolfram A1 - Resch-Genger, Ute T1 - C⁠3A passivation with gypsum and hemihydrate monitored by optical spectroscopy N2 - Tricalcium aluminate (C⁠3A) is found with less than 10% wt. of the total composition; however, during hydration, C⁠3A plays an important role in the early hydration of cement in the presence of gypsum as a set retarder. The aim of this investigation is to assess the suitability of optical spectroscopy and a dye-based optical probe to monitor early hydration of C⁠3A in the presence of gypsum and hemihydrate. Optical evaluation was performed using steady-state fluorescence and diffuses reflectance spectroscopy (UV-VisDR). Phase characterization during hydration was done with in-situ X-ray diffraction. UV-VisDR with a cyanine dye probe was used to monitor the formation of metastable phases and was employed together with fluorescence spectroscopy, to follow the Aggregation and disaggregation of the dye during hydration. In conclusion, for the first time, a cyanine dye was identified as a feasible and stable probe to monitor C⁠3A hydration changes in the presence of calcium sulfate. KW - Dye KW - Photoluminescence KW - Fluorescence KW - Reflection spectroscopy KW - Cement KW - Hydration KW - Method development PY - 2020 DO - https://doi.org/10.1016/j.cemconres.2020.106082 VL - 133 SP - 106082 PB - Elsevier Ltd. CY - Amsterdam AN - OPUS4-50952 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Schmidt, Wolfram A1 - Weba, Luciana A1 - Silbernagl, Dorothee A1 - Mota Gassó, Berta A1 - Höhne, Patrick A1 - Sturm, Heinz A1 - Pauli, Jutta A1 - Resch-Genger, Ute A1 - Steinborn, Gabriele ED - Khayat, Kamal Henry T1 - Influences of nano effects on the flow phenomena of self-compacting concrete N2 - Chemical admixtures like superplasticisers or stabilising agents are of ever increasing importance for modern concrete technology. They liberate the workability of concrete from its dependency on water content, and thus, open the gate towards innovative and future oriented concrete technologies such as selfcompacting concrete. Meanwhile admixtures have become common practice in concrete technology, but the understanding of these highly complex polymers in the entire concrete system lags far behind their application. Due to its complex time-dependent, multi-phase and multi-scale behaviour, flowable concrete systems are highly complicated and cannot be described comprehensively by simple models. It is therefore extremely challenging to identify the relevant parameters that predominantly control flow phenomena on different size scales, since these may occur on any scale between the nano scale (e.g. superplasticizer adsorption) and macro scale (e.g. grading of the aggregates). The present study discusses fundamental mechanisms at the interface between particle or hydrate surfaces and the fluid phase at a very early stage of concrete formation, and links these effects to macroscopic flow phenomena. Methods are discussed that appear promising interdisciplinary tools for enhancement of the understanding of the relevant interactions that are responsible for the macroscopic flow of flowable concrete. T2 - 8th International RILEM Symposium on Self-Compacting Concrete CY - Washington, D.C., USA DA - 15.05.2016 KW - Adsorption KW - Analytics KW - Hydration KW - Polycarboxylate ether KW - Rheology PY - 2016 SP - 245 EP - 254 AN - OPUS4-36882 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Schmidt, Wolfram A1 - Mota Gassó, Berta A1 - Sturm, Heinz A1 - Pauli, Jutta ED - Greim, M. ED - Kusterle, W. ED - Teubert, O. T1 - Influence of effects on nano and micro scale on the rheological performance of cement paste, mortar and concrete N2 - Chemical admixtures like superplasticisers or stabilising agents are of ever increasing importance for modern concrete technology. They liberate the workability of concrete from its dependency on water content, and thus, open the gate towards innovative and future oriented concrete technologies such as self-compacting concrete. Today, admixture addition has become common practice in concrete technology, but the understanding of their highly complex mode of operation is extremely difficult and demands for understanding of processes within the range between nanometres and centimetres. Due to its complex time-dependent, multi-phase and multi-scale behaviour, flowable concrete systems are highly complicated and cannot be described comprehensively by simple models. It is therefore extremely challenging to identify the relevant parameters that predominantly control flow phenomena on different size scales, since these may occur on any scale between the nano scale (e.g. superplasticizer adsorption) and macro scale (e.g. grading of the aggregates). The present study discusses fundamental mechanisms at the interface between particle or hydrate surfaces and the fluid phase at a very early stage of concrete formation, and links these effects to macroscopic flow phenomena. Methods are discussed that appear promising interdisciplinary tools for enhancement of the understanding of the relevant interactions that are responsible for the macroscopic flow of flowable concrete. T2 - 25. Workshop und Kolloquium Rheologische Messsungen an Baustoffen CY - Regensburg, Germany DA - 02.03.2016 KW - Rheology KW - Cement KW - Concrete KW - Superplasticizer KW - Nano scale PY - 2016 SN - 978-3-7345-1313-8 SP - 294 EP - 307 PB - tredition CY - Hamburg AN - OPUS4-36862 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Pauli, Jutta T1 - Certified Fluorescence Quantum Yield Standards as New Optical Reference Materials N2 - Luminescence techniques are amongst the most commonly used analytical methods in life and material sciences due to their sensitivity and their nondestructive and multiparametric character. Photoluminescence signals are, however, affected by wavelength, polarization and time dependent instrument specific effects, and provide only relative intensities. This hampers the comparability of fluorescence measure-ments and calls for simple tools for instrument characterization and the quantification of measured fluorescence intensities. Well characterized fluorescence standards for instrument calibration and performance validation (IPV) can be used as references for fluorescence signals. Of special importance is the correct determination of photoluminescence quantum yields (QF) (number of emitted per absorbed photons) that provides a direct comparison of the fluorescence efficiency of emitters. Such well characterized standards have been successfully developed by BAM for the relative determination of f values of transparent solutions of molecular and nanoscale emitters in the wavelength range from 350 and 1100 nm and will be soon certified. These standards can also be used to evaluate integrating sphere setups, which are increasingly being used for absolute measurements of QF values. T2 - ANAKON 2019 CY - Münster, Germany DA - 25.03.2091 KW - Fluoreszenz KW - Referenzmaterial PY - 2019 AN - OPUS4-47795 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER -