TY - GEN A1 - Brookes, S. A1 - Scholz, A. A1 - Klingelhöffer, Hellmuth A1 - Whittaker, M. A1 - Loveday, M. A1 - Wisby, A. A1 - Ryder, N. A1 - Lohr, R. A1 - Stekovic, S. A1 - Moverare, J. A1 - Holdsworth, S. A1 - Dudzinski, D. T1 - Code of practice for force-controlled thermo-mechanical fatigue testing N2 - Components in the Aerospace, Power and Automotive engineering sectors are frequently subjected to cyclic stresses induced by thermal fluctuations and mechanical loads. For the design of such components, reliable material property data are required which need to be acquired using well accepted and reproducible test procedures for thermo-mechanical fatigue (TMF) loading. Available materials TMF property data are limited so that there is a need for further TMF data generated by TMF testing. The TMF behaviour of materials is often desired to be simulated in models which describe the cyclic stress-strain behaviour, the fatigue life and the cyclic crack growth behaviour. There is a continuous need for the development and amendment of such models. Models can be validated by using materials in industrial applications which are subjected to TMF loading. KW - Force controlled TMF testing PY - 2015 UR - http://www.tmf-workshop.bam.de/en/tmf_media/code_of_practice_for_force_controlled_thermo-mechanical_fatigue_(2).pdf SP - 1 EP - 32 AN - OPUS4-35248 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - GEN A1 - Dörfel, Ilona A1 - Steinborn, Gabriele A1 - Langner, Jeanette A1 - Krietsch, Arne A1 - Seeger, Stefan A1 - Österle, Werner A1 - Schmidt, Martin A1 - Bresch, Harald T1 - Dossier on titanium dioxide - Part 1/1 - NM 105 N2 - In November 2007, OECD’s Working Party on Manufactured Nanomaterials (WPMN) launched the Sponsorship Programme for the Testing of Manufactured Nanomaterials (hereafter the Testing Programme). The objective was to conduct specific tests, relevant to human health and environmental safety endpoints, on a variety of manufactured nanomaterials (MN). The outcomes of the Testing Programme were intended to assess the applicability of the existing test guidelines1 to nanomaterials, as well as to provide useful information on any intrinsic properties of MNs, which are different from the same bulk material with greater external dimensions. Understanding the properties of NMs is crucial to choose appropriate strategies for hazard identification, risk assessment or risk management measures. The Testing Programme involved delegations from OECD member countries, some non-member economies and other stakeholders. The broad international representation, from a range of delegations enabled the programme to pool expertise and resources without which this programme would not have been possible. KW - Nanomaterial KW - Nanoparticle KW - Sponsorship programme KW - Nano characterization PY - 2015 UR - http://www.oecd.org/env/ehs/nanosafety/dossier-on-silver-nanoparticles-part1-1.htm IS - 54 SP - 27 CY - Paris AN - OPUS4-35430 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - GEN A1 - Wiesner, Anja A1 - Neumann, Patrick P. A1 - Krentel, Daniel A1 - Patzelt, Anne-Katrin T1 - Übersicht IFAFRI Capability Gaps N2 - Die zehn Capability Gaps der IFAFRI (International Forum to Advance First Responder Innovation) werden zusammengefasst und übersichtlich dargestellt. KW - BOS KW - KMU KW - IFAFRI KW - Security KW - Safety PY - 2021 SP - 1 EP - 10 CY - Berlin AN - OPUS4-53624 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - GEN A1 - Asbach, C. A1 - Held, A. A1 - Kiendler-Scharr, A. A1 - Scheuch, G. A1 - Schmid, H.-J. A1 - Schmitt, S. A1 - Schumacher, S. A1 - Wehner, B. A1 - Weingartner, E. A1 - Weinzierl, B. A1 - Bresch, Harald A1 - Seeger, Stefan A1 - u.a., T1 - Position paper of the Gesellschaft für Aerosolforschung on understanding the role of aerosol particles in SARS-CoV-2 infection N2 - Many studies have already shown that viruses can spread via aerosol particles. An aerosol is a mixture of air with solid or liquid particles dispersed in it. To understand the role of aerosol particles as a transmission path of SARS-CoV-2, knowledge of the different processes in an Aerosol is therefore of particular importance. With this paper, GAeF would like to contribute to a better understanding of the term “aerosol” and the relevant aerosol processes. In the context of this paper only the essential basics will be discussed. For a deeper understanding of the partly complex processes, please refer to the literature mentioned at the end of the paper. The paper summarises a large number of studies on the formation of virus-laden aerosol particles and their spread. Based on this, it can be concluded that exhaled aerosol particles may play a prominent role in the spread of viruses in the corona pandemic. Finally, this paper discusses possible measures to reduce the spread of aerosol particles. The measures discussed are based on the current public debate including ventilation, air purifiers, HVAC systems and masks. Advice is given on the correct and sensible use of these measures. An aerosol is always dynamic, as particles are newly formed, transported in or with the air, removed from the air or change in the airborne state. Aerosol particles have sizes between approx. 0.001 and several 100 micrometres (and not < 5 μm as currently defined in many publications) and spread relatively quickly with air currents, even over longer distances. Larger aerosol particles sink to the ground, depending on their size and density, while small aerosol particles can remain in the air for a very long time (see Section 3). Every person emits liquid aerosol particles of various sizes through breathing and when speaking, coughing and sneezing (see Section 4). If a person is infected with a virus, such as SARS-CoV-2, these aerosol particles can contain viruses that can be released into the air and inhaled by other people. SARS-CoV-2 has a size of 0.06 to 0.14 micrometres, but the exhaled liquid aerosol particles are larger. The liquid aerosol particles can shrink by evaporation, depending on the ambient conditions (see Section 3.3). Particle size is relevant for particle transport and particle separation. The highest risk of infection exists in closed indoor spaces, as aerosol particles can accumulate there. Here in particular, appropriate measures must be taken to reduce the concentration of aerosol particles (see Section 5). Against the background of aerosol science, the GAeF classifies the current measures to contain the pandemic as follows: • In principle, no measure can work on its own! According to the current state of knowledge, the interaction of the most varied measures is the best way to minimise the risk of infection. • Keeping distance is important, because with increasing distance, directly exhaled viruses are diluted and the probability of infection decreases. The often prescribed minimum distance can be used as a guide, but it should be increased and supplemented by other measures (see below), especially for longer meetings and also indoors with reduced air movement. • Masks help to filter some of the exhaled particles (and viruses). This reduces the concentration of exhaled particles (and viruses) in a room and thus the risk of infection. It should be noted here that the exhaled aerosol particles are relatively large due to adhering moisture and can therefore also be efficiently retained by simple masks. However, since these particles shrink with longer dwell time in the room air, simple mouth-nose masks are less efficient for self-protection. Respiratory masks are required for this purpose, which show a high degree of separation even for fine particles, e.g. of classes FFP2, N95 or KN95. These are efficient for both self-protection and protection of others unless they have an exhalation valve. Masks with an exhalation valve, on the other hand, are only for self-protection and therefore contradict the solidarity concept that fellow human beings are protected by collective mask wearing. Face shields which are used without additional masks are largely useless with regard t• aerosol particles, as the air with particles (and viruses) flows unfiltered around the shields. In everyday clinical practice, facial shields are worn in addition to masks to prevent droplet infection via the mucous membranes of the eyes. Mobile or permanently installed Plexiglas barriers are also largely ineffective against the spread of aerosols indoors. These can only prevent the smallscale spread of an aerosol in the short term, e.g. in the checkout area of a supermarket, but offer no protection in the longer term. Face shields and Plexiglas panels essentially serve as spit and splash protection against large droplets. • Outdoors, there are practically no infections caused by aerosol transmission. However, droplet infections can still occur, especially in crowds, if minimum distances are not observed and/or masks are not worn. In closed rooms, ventilation is essential to replace the exhaled air in a room with fresh air from outside. Frequent airing and cross-ventilation is just as effective as leaving the window open all the time. From an energy point of view, however, it is more efficient to ventilate the room, especially in winter. CO2 monitors can help to monitor indoor air quality. They indicate when it is necessary to ventilate and when the air in a room has been sufficiently changed during ventilation. However, they can only be used as an indicator and even if the proposed CO2 limit concentrations are met, they do not prevent direct infection by people in the immediate vicinity. • Air purifiers can make a useful contribution to reducing the concentration of particles and viruses in a room. When procuring air purifiers, care must be taken to ensure that they are adequately dimensioned for the room and application in question in order to significantly reduce the particle and virus load. The air throughput of the unit is more important than the pure efficiency of the filter. For energy and cost reasons, the use of highly efficient filters can even be counterproductive. Permanently installed ventilation systems can also be useful, provided they filter the air to reduce the particle and virus load in a room. To avoid infections, it is advisable to operate them with 100 % fresh air if possible. From the point of view of the Gesellschaft für Aerosolforschung, there is a considerable need for research, especially at the interdisciplinary borders to research fields of epidemiology, infectiology, virology, ventilation technology and fluid mechanics. The implementation of targeted studies should be made possible at short notice with special funding and research programmes. This paper was written originally in German by members of the Gesellschaft für Aerosolforschung and is supported by a large number of international aerosol experts. Both the English and German version as well as all images in the paper are available for free download at the following link: https://www.info.gaef.de/positionspapier. The “Gesellschaft für Aerosolforschung e. V.” must be named as the source, whenever an image is used. KW - COVID KW - SARS KW - GAeF KW - Aerosol KW - Corona PY - 2021 UR - https://www.info.gaef.de/_files/ugd/fab12b_d8d88393f90240cdbea63c88c09887ef.pdf DO - https://doi.org/10.5281/zenodo.4350494 SP - 1 EP - 48 PB - Association for Aerosol Research CY - Köln AN - OPUS4-53955 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - GEN A1 - Steglich, P. A1 - Rabus, D. G. A1 - Sada, C. A1 - Paul, Martin A1 - Weller, Michael G. A1 - Mai, C. A1 - Mai, A. T1 - Silicon Photonic Micro-Ring Resonators for Chemical and Biological Sensing: A Tutorial N2 - Silicon photonic micro-ring resonators (MRR) developed on the silicon-on-insulator (SOI) platform, owing to their high sensitivity and small footprint, show great potential for many chemical and biological sensing applications such as label-free detection in environmental monitoring, biomedical engineering, and food analysis. In this tutorial, we provide the theoretical background and give design guidelines for SOI-based MRR as well as examples of surface functionalization procedures for label-free detection of molecules. After introducing the advantages and perspectives of MRR, fundamentals of MRR are described in detail, followed by an introduction to the fabrication methods, which are based on a complementary metal-oxide semiconductor (CMOS) technology. Optimization of MRR for chemical and biological sensing is provided, with special emphasis on the optimization of waveguide geometry. At this point, the difference between chemical bulk sensing and label-free surface sensing is explained, and definitions like waveguide sensitivity, ring sensitivity, overall sensitivity as well as the limit of detection (LoD) of MRR are introduced. Further, we show and explain chemical bulk sensing of sodium chloride (NaCl) in water and provide a recipe for label-free surface sensing. KW - Lab on a chip KW - Biosensor KW - Cmos KW - Silanization KW - Surface derivatization KW - Evanescent wave PY - 2021 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-529360 DO - https://doi.org/10.36227/techrxiv.14909901.v1 SP - 1 EP - 18 PB - IEEE CY - Piscataway Township AN - OPUS4-52936 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - GEN A1 - Tchipilov, Teodor A1 - Raysyan, Anna A1 - Weller, Michael G. T1 - Methods for the quantification of particle-bound protein – Application to reagents for lateral-flow immunoassays (LFIA) N2 - Protein immobilization for the functionalization of particles is used in various applications, including biosensors, lateral-flow immunoassays (LFIA), bead-based assays, and others. Common methods for the quantification of bound protein are measuring protein in the supernatant before and after coating and calculating the difference. This popular approach has the potential for a significant overestimation of the amount of immobilized protein since layers not directly bound to the surface (soft protein corona) are usually lost during washing and handling. Only the layer directly bound to the surface (hard corona) can be used in subsequent assays. A simplified amino acid analysis method based on acidic hydrolysis and RP-HPLC-FLD of tyrosine and phenylalanine (aromatic amino acid analysis, AAAA) is proposed to directly quantify protein bound to the surface of gold nano- and latex microparticles. The results are compared with indirect methods such as colorimetric protein assays, such as Bradford, bicinchoninic acid (BCA), as well as AAAA of the supernatant. For both particle types, these indirect quantification techniques show a protein overestimation of up to 1700% compared to the direct AAAA measurements. In addition, protein coating on latex particles was performed both passively through adsorption and covalently through EDC/sulfo-NHS chemistry. Our results showed no difference between the immobilization methodologies. This finding suggests that usual protein determination methods are no unambiguous proof of a covalent conjugation on particles or beads. KW - Soft protein corona KW - Hard protein corona KW - Gold particles KW - Nanoparticles KW - Mikroparticles KW - Antibody KW - Bioconjugation KW - Protein quantification KW - Supernatant KW - Sodium chloride method KW - Covalent conjugation KW - Latex particles KW - Lateral flow immunoassays PY - 2022 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-545365 DO - https://doi.org/10.20944/preprints202203.0332.v1 SP - 1 EP - 8 PB - MDPI CY - Basel AN - OPUS4-54536 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - GEN A1 - Gabler, Mariella T1 - Development of an affinity-based method for the site-selective synthesis of antibody-drug-conjugates N2 - For the site-selective synthesis of ADCs, a variety of obstacles must be overcome. Those include designing bifunctional affinity peptides with reasonably low 𝐾𝑑-values that couple to the mAb in a site-selective manner. These peptides should also include a functional group that links the payload to the mAb under mild conditions without adversely affecting it. The bioconjugation between peptide and antibody and the linker between peptide and payload must be stable and durable to provide safety when used for medical purposes. The usage of metals and organic solvents should be minimized. Within the project, new types of functionalized affinity peptides were designed, and their affinity towards the Fc-fragment was determined. KW - Antibody drug conjugate KW - ADC KW - Human antibody KW - Peptide KW - Linker KW - Toxin KW - Payload KW - Monomethyl Auristatin E KW - MMAE KW - DM1 KW - Click chemistry KW - Copper-catalyzed KW - SDS-PAGE KW - HPLC KW - Trastuzumab KW - Herceptin KW - SPR KW - MALDI-TOF-MS KW - Mertansine KW - Site-selective bioconjugation KW - Affinity PY - 2021 SP - 1 EP - 100 PB - Humboldt-Universität zu Berlin CY - Berlin AN - OPUS4-54519 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - GEN A1 - Taube, Peter T1 - Development of columns based on glass monoliths for affinity chromatography N2 - The aim of this work was the preparation of a novel stationary monolithic phase for affinity chromatography and HPLC-applications. Therefore, we have chosen porous glass filters that are available with different pore sizes as raw materials to prepare monolithic columns. We purchased VitraPOR 4 (10-16 μm pore size) and VitraPOR 5 (1.0-1.6 μm pore size) monolithic glass filters. The physical properties of these glass filters were characterized. The surface area, pore size distribution and the porosity were determined using mercury intrusion porosimetry and BET. These glass filters only exhibit flow through pores and therefore show no bimodal pore size distribution in the mercury intrusion curves. Due to their low permeability, the applied filters that exhibit an inner diameter of 8.0 mm and a length of 15.0±0.1 mm could be operated at flow rates more than 10 ml/min. High flow rates are favorable for fast separation experiments. KW - Monolith KW - Affinity chromatography KW - Affinity extraction KW - Borosilicate glass KW - Sintered KW - Surface area KW - Flow rate KW - VitraPOR KW - Pressure KW - Protein A KW - Dynamic binding capacity KW - Protein A cys KW - Column regeneration KW - Performance comparison PY - 2017 SP - 1 EP - 102 PB - Humboldt-Universität zu Berlin CY - Berlin AN - OPUS4-54564 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - GEN A1 - Babutzka, Martin A1 - et al., T1 - Exposure Site Catalogue - Catalogue of atmospheric corrosion field exposure sites in Europe N2 - Exposure sites and outdoor exposure have always been a part of atmospheric corrosion research providing the “final answer”, although at the cost of long exposure times. Individual exposure programs such as ISOCORRAG, MICAT and ICP Materials have resulted in collaborative networks of exposure sites. So far, however, there has been no collective effort to put together currently active sites in a comprehensive manner and across programs and nations. The information collected in the catalogue is possible thanks to the work of all individual site managers listed as contact persons, efforts of members of Working Party 25 (WP25) Atmospheric Corrosion of the European Federation of Corrosion (EFC) and financial support of the EFC. With this Catalogue you can both get a general overview of what is available and be guided if you are looking for a particular environment with certain characteristics. KW - Atmospheric Corrosion KW - Atmosphärische Korrosion KW - Corrosion KW - Korrosion KW - Exposure KW - Auslagerungsversuche PY - 2022 UR - https://efcweb.org/Scientific+Groups/WP25_+Atmospheric+Corrosion/Current+Activities/_/Exposure%20site%20catalogue%20EFC%20lores.pdf SP - 1 EP - 56 PB - European Federation of Corrosion, EFC AN - OPUS4-55284 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - GEN A1 - Paul, Martin T1 - Microarrays for the screening of monoclonal antibodies from supernatants N2 - In this thesis a protocol based on a direct competitive and non-competitive immunoassay using the microarray format was developed to screen emulated hybridoma supernatants against the drug carbamazepine (CBZ). As support, epoxy slides were manufactured by coating microscope glass slides with epoxy silanes. The manufactured epoxy slides showed similar capacity for protein immobilization as commercially available NEXTERION slides, but showed a higher autofluorescence background. On the epoxy slides, protein A, Cys-A, G and Cys-G were immobilized as antibody capturing coating. It could be shown that the Cys-tag considerably increased the immobilization of all compared proteins, especially of protein G. Protein Cys-G immobilized at pH 8-9 was considered the most suitable protein for antibody immobilization due to good spot uniformity and a high binding capacity for IgG. Additionally, in immobilization experiments it could be shown, that 10-500 fold excess of bovine IgG, introduced by two different fetal bovine serum (FBS) products, showed no significant competition on the immobilization of mice or goat IgG on protein Cys-G. To examine the captured antibodies for affinity to CBZ, the CBZ-TOTA-DY654 tracer was custom synthesized. It could be demonstrated, that the tracer antibody interaction was competitive with the tracer precursor, CBZ-TOTA-NH2 and CBZ. Furthermore, the synthesized tracer was also successfully used by externals to evaluate CBZ affine hybriodoma cells in flow cytometry. In the simulated screening, five antibodies with known affinity to CBZ were diluted in a cell culture medium. The screening method allowed to differentiate between affine antibodies (IC50 < 20 µg/ml) and unaffine antibodies (IC50 > 20 µg/ml), when concentrations of 0.1 µg/ml IgG or greater have been used. Of five applied antibodies, all highly affine clones (CE2 and B3212M) were reported as positives while no false-positive samples were observed. The screening included competitive, with around 89500 fold excess of CBZ, and non-competitive tracer incubation on different segments of the same chip, which resulted in total signal suppression on the competitive segment. The screening was performed in 20 hours, only a few nanoliters, of each simulated supernatant, were consumed in the screening process, furthermore in the method standard 96 well MTPs were used and no cleanroom facilities were required. KW - Carbamazepine KW - Microscopic slides KW - Protein A cys KW - Competition KW - Epoxy silanes KW - Supernatant KW - Antibody immobilization PY - 2017 SP - 1 EP - 96 PB - Humboldt-Universität zu Berlin CY - Berlin AN - OPUS4-54645 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER -