TY - GEN A1 - Wiegner, Katharina A1 - Farke, M. A1 - Horn, Wolfgang A1 - Jann, Oliver A1 - Hahn, Oliver ED - Brozio, P. T1 - Schadstoffe im Museum richtig einschätzen N2 - Schadstoffe beschäftigen derzeit Museen weltweit Heute weiß man, dass diese auch aus Materialien, die für den Ausstellungsbau verwendet werden, austreten können, was eine Gefahr für Exponate darstellt. Ein neues Verfahren namens BEMMA bietet nun erstmalig die Möglichkeit, relativ schnell und effektiv eine problemorientierte Untersuchung und Bewertung mit belastbaren und reproduzierbaren Ergebnissen vorzunehmen. KW - Emissionsarme Vitrinen KW - Präventive Konservierung KW - VOC KW - BEMMA PY - 2011 SN - 978-3-7667-1962-1 SP - 127 EP - 131 PB - Callwey CY - München AN - OPUS4-25377 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Wiegner, Katharina A1 - Hahn, Oliver A1 - Farke, M. A1 - Kalus, Sabine A1 - Horn, Wolfgang T1 - Determination of formic and acetic acids in air N2 - Formic and acetic acids are often responsible for damage of cultural objects, e. g. glass and metal corrosion or changing and fading of colours. Museums all around the world are equipped with different show cases. Display cases should protect cultural objects from dust as well as from mechanical damage. Several construction materials which are used for display cases, including wood, glue and coatings, are possible sources of very volatile organic compounds (VVOCs), volatile organic compounds (VOCs) and semi volatile organic compounds (SVOCs). These construction products can emit formic and acetic acids into the indoor or display case air. Modern display cases with small air change rates can cause higher concentrations of formic and acetic acids if any source is installed in the display case (Salthammer and Uhde, 2009). To minimize the risk of damage emissions from building products must be quantified. There is a need for a method for identification and quantification of acetic and formic acid. Some possibilities for the identification of acetic acid exist. The quantification of acetic acid for example after sampling on TENAX® or CARBOTRAP and thermal desorption-GC in accordance with ISO 16000-6 and ISO 16017-1 results in very low recovery rates. A new method should be stabile, robust, reproducible and comparable, with an easy local sampling and determination in laboratories. Miniaturised emission test chambers and model display cases were used to study the recovery rates. T2 - Indoor Air 2011, 12th International conference on indoor air quality and climate CY - Austin, TX, USA DA - 05.06.2011 KW - VOCs KW - Detection of formic and acetic acid KW - Quantification of formic and acetic acid KW - Air sampling PY - 2011 IS - Paper 768 SP - 1 EP - 2 AN - OPUS4-23876 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Wiegner, Katharina A1 - Hahn, Oliver A1 - Horn, Wolfgang A1 - Farke, M. A1 - Kalus, Sabine A1 - Nohr, Michael A1 - Jann, Oliver T1 - Determination of formic and acetic acid emissions in indoor air or from building products N2 - Several construction and building materials, including wood, glue and coatings, are possible sources of very volatile organic compounds (VVOCs) and volatile organic compounds (VOCs) like formic and acetic acid. Due to very high air tightness and very low air exchange rates in new buildings concentrations of these harmful substances can increase considerably. To minimize the risk, emissions from building products should be identified and quantified. With the common standard method, this means Tenax® sampling followed by thermal desorption and GC-MS analysis, these acids could not be detected sufficiently. The aim oft this study is the comparison of two different methods for the determination of acetic and formic acid. The sampling of method one, which is usually used for identification and quantification of VOCs, is done in accordance with ISO 16000-6 and ISO 16017-1 on Carbotrap® 202 multi-bed thermal desorption tube by subsequent identification and quantification with GC-MS. Method two is based on sampling on 2,4-dinitrophenylhydrazine (DNPH) cartridges, derivatisation, elution, identification and quantification of the derivatives with LC-MS/MS (liquid chromatography – mass spectrometry/mass spectrometry). N2 - Viele Konstruktions- und Baumaterialien, wie Holz, Kleber und Anstriche, sind mögliche Quellen für leicht flüchtige organische Verbindungen (VVOC) und flüchtige organische Verbindungen (VOC), wie Ameisen- und Essigsäure. Bedingt durch die hohe Dichtigkeit und den damit verbundenen niedrigen Luftwechsel in neuen Gebäuden können die Konzentrationen dieser gesundheitsgefährdenden Substanzen beträchtlich ansteigen. Um das Risiko zu minimieren, sollen Emissionen aus Bauprodukten identifiziert und quantifiziert werden. Mit der üblichen Standardmethode, die auf einer Luftprobenahme auf Tenax® und anschließender Analyse mittels GC-MS basiert, können diese Säuren nicht ausreichend detektiert werden. Ziel dieser Arbeit ist der Vergleich von zwei unterschiedlichen Methoden zur Bestimmung von Essig- und Ameisensäure. Die Luftprobenahme der ersten Methode, die üblicherweise zur Identifizierung und Quantifizierung von VOC genutzt wird, wurde gemäß ISO 16000-6 and ISO 16017-1 auf Carbotrap® 202, ein mit mehreren Adsorbentien gepacktes Thermodesorptionsrohr, mit anschließender Identifikation und Quantifizierung mittels GC-MS durchgeführt. Die zweite Methode basiert auf einer Luftprobenahme mittels 2,4-Dinitrophenylhydrazin-(DNPH)-Kartuschen, Derivatisierung, Elution, Identifikation und Quantifizierung der Derivate mit LC-MS/MS (Flüssigkeitschromatographie – Massenspektometrie/Massenspektometrie). KW - Formic acid KW - Acetic acid KW - VVOCs KW - Air sampling KW - DNPH PY - 2012 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-255911 UR - http://www.gefahrstoffe.de/gest/article.php?data[article_id]=65887 SN - 0949-8036 SN - 0039-0771 SN - 1436-4891 VL - 72 IS - 3 SP - 84 EP - 88 PB - Springer-VDI-Verlag CY - Düsseldorf AN - OPUS4-25591 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Wiegner, Katharina A1 - Farke, M. A1 - Horn, Wolfgang A1 - Jann, Oliver A1 - Hahn, Oliver T1 - Den Schadstoffen auf der Spur - Die Bewertung von Emissionen aus Materialien für Museumsausstattungen mithilfe des neuen BEMMA-Schemas N2 - Ausstellungskuratoren, Restauratoren oder Fachplaner stehen immer wieder vor der Entscheidung, geeignete Materialien für Museumsausstattungen auswählen zu müssen. Vitrinen, Depoteinrichtungen, aber auch Transportverpackungen für Kunst- und Kulturgut sollten unbedingt frei von Schadstoffen sein. Ein neues Verfahren ermöglicht nun eine problemorientierte Untersuchung und Bewertung von Materialien mit belastbaren und reproduzierbaren Ergebnissen. KW - BEMMA KW - Emissionsarme Vitrine KW - Schadstoffe PY - 2012 SN - 0933-4017 VL - 3 SP - 38 EP - 44 PB - Callwey CY - München AN - OPUS4-25794 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Wiegner, Katharina A1 - Horn, Wolfgang A1 - Stephan, Ina A1 - Nohr, Michael A1 - Lau, Angelika A1 - Farke, M. A1 - Hahn, Oliver T1 - Überprüfung möglicher mikrobieller Belastungen in Vitrinenluft durch Kleinklimageräte N2 - Unterschiedliche Befeuchtungssysteme für Vitrinen, die die Ausstellungsobjekte bei definierter Luftfeuchtigkeit vor externen Einflüssen wie Staub bewahren sollen, wurden im Hinblick auf die Möglichkeit der potenziellen mikrobiologischen Kontamination untersucht. Ergänzend hierzu wurden Parameter wie pH-Wert und Leitfähigkeit des Wassers im Befeuchter untersucht und die mikrobiellen flüchtigen organischen Verbindungen (MVOC, microbial volatile organic compounds) in der Modellvitrine bestimmt. Die Leitfähigkeitsmessung kann als Indikator für den Verunreinigungsgrad des Wassers dienen, weil sie mit der mikrobiologischen Belastung korreliert. Weiterhin war eine mikrobiologische Belastung der Luft in der Modellvitrine auch bei relativ hoher Verunreinigung des Befeuchtungswassers nicht nachzuweisen. KW - MVOC (microbial volatile organic compounds) KW - Schimmelpilze KW - Kleinklimagerät KW - Vitrinen KW - Essigsäure PY - 2011 SN - 0949-8036 SN - 0039-0771 SN - 1436-4891 VL - 71 IS - 9 SP - 378 EP - 381 PB - Springer-VDI-Verl. CY - Düsseldorf AN - OPUS4-24340 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Wiegner, Katharina A1 - Hahn, Oliver A1 - Farke, M. A1 - Stephan, Ina A1 - Nohr, Michael A1 - Horn, Wolfgang T1 - Development of methods for testing of microbiological contamination of small climate control units for air in display cases T2 - Healthy Buildings 2012 - 10th International conference CY - Brisbane, Australia DA - 2012-07-08 KW - Microbiological contamination KW - Acetic and formic acid KW - Conductivity KW - Climate control device KW - Display case KW - Normung KW - Geruch KW - Messmethoden KW - Emissionsmessung KW - Bauprodukte PY - 2012 SN - 978-1-921897-40-5 SP - 1 EP - 2 (5H.2) AN - OPUS4-27562 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Hahn, Marc Benjamin A1 - Dietrich, P. M. A1 - Radnik, Jörg T1 - In situ monitoring of the influence of water on DNA radiation damage by near-ambient pressure X-ray photoelectron spectroscopy N2 - Ionizing radiation damage to DNA plays a fundamental role in cancer therapy. X-ray photoelectron-spectroscopy (XPS) allows simultaneous irradiation and damage monitoring. Although water radiolysis is essential for radiation damage, all previous XPS studies were performed in vacuum. Here we present near-ambient-pressure XPS xperiments to directly measure DNA damage under water atmosphere. They permit in-situ monitoring of the effects of radicals on fully hydrated double-stranded DNA. The results allow us to distinguish direct damage, by photons and secondary low-energy electrons (LEE), from damage by hydroxyl radicals or hydration induced modifications of damage pathways. The exposure of dry DNA to x-rays leads to strand-breaks at the sugar-phosphate backbone, while deoxyribose and nucleobases are less affected. In contrast, a strong increase of DNA damage is observed in water, where OH-radicals are produced. In consequence, base damage and base release become predominant, even though the number of strand-breaks increases further. KW - DNA KW - XPS KW - NAP-XPS KW - Radiation damage KW - Single-strand break (SSB) KW - Double-strand break (DSB) KW - Xray KW - OH radical KW - Hydroxyl radical KW - LEE KW - Low energy electrons KW - Dosimetry KW - Geant4 KW - Geant4-DNA KW - TOPAS KW - TOPAS-nbio KW - Microdosimetry KW - DNA radiation damage KW - Direct damage KW - Indirect damage KW - Quasi-direct damage KW - Hydration shell KW - Dry DNA KW - Hydrated DNA KW - ROS KW - Radical KW - Reactive oxygen species KW - Net-ionization reaction KW - Radiation therapy KW - Cancer therapy KW - Xray photo electron spectrocopy KW - Near ambient pressure xray photo electron spectroscopy KW - Base damage KW - Base loss KW - Dissociative electron transfer (DET) KW - Dissociative electron attachment (DEA) KW - Hydrated electron KW - Prehydrated electron KW - Ionization KW - PES PY - 2021 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-524060 DO - https://doi.org/10.1038/s42004-021-00487-1 SN - 2399-3669 VL - 4 IS - 1 SP - 50 PB - Springer Nature CY - London AN - OPUS4-52406 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Hahn, Marc Benjamin A1 - Zutta Villate, J. M. ED - Zutta Villate, J. M. T1 - Combined cell and nanoparticle models for TOPAS to study radiation dose enhancement in cell organelles N2 - Dose enhancement by gold nanoparticles (AuNP) increases the biological effectiveness of Radiation damage in biomolecules and tissue. To apply them effectively during cancer therapy their influence on the locally delivered dose has to be determined. Hereby, the AuNP locations strongly influence the energy deposit in the nucleus, mitochondria, membrane and the cytosol of the targeted cells. To estimate these effects, particle scattering simulations are applied. In general, different approaches for modeling the AuNP and their distribution within the cell are possible. In this work, two newly developed continuous and discrete-geometric models for simulations of AuNP in cells are presented. These models are applicable to simulations of internal emitters and external radiation sources. Most of the current studies on AuNP focus on external beam therapy. In contrast, we apply the presented models in Monte-Carlo particle scattering simulations to characterize the energy deposit in cell organelles by radioactive 198AuNP. They emit beta and gamma rays and are therefore considered for applications with solid tumors. Differences in local dose enhancement between randomly distributed and nucleus targeted nanoparticles are compared. Hereby nucleus targeted nanoparticels showed a strong local dose enhancement in the radio sensitive nucleus. These results are the foundation for future experimental work which aims to obtain a mechanistic understanding of cell death induced by radioactive 198Au. KW - AuNP KW - Beta decay KW - Brachytherapy KW - Cancer treatment KW - DNA KW - DNA damage KW - Dosimetry KW - Energy deposit KW - Geant4 KW - Geant4-DNA KW - Gold Nanoparticles KW - LEE KW - MCS KW - Microdosimetry KW - Monte-Carlo simulation KW - NP KW - Ectoine KW - OH radicals KW - Radiation damage KW - Radiationtherapy KW - Radioactive decay KW - Simulation KW - Beta particle KW - Clustered nanoparticles KW - Gamma ray KW - Low energy electrons KW - Particle scattering KW - Radiolysis KW - Livermore model KW - Penelope model KW - TOPAS KW - TOPAS-nbio PY - 2021 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-523276 DO - https://doi.org/10.1038/s41598-021-85964-2 SN - 2045-2322 VL - 11 IS - 1 SP - 6721 PB - Springer Nature AN - OPUS4-52327 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Waiblinger, H. U. A1 - Brockmeyer, J. A1 - Bruenen-Nieweler, C. A1 - Busch, U. A1 - Haase, I. A1 - Hahn, A. A1 - Haarmann, M. A1 - Hauser, W. A1 - Huber, I. A1 - Jany, K. D. A1 - Kirmse, N. A1 - Lindeke, S. A1 - Neumann, K. A1 - Naumann, H. A1 - Paschke, A. A1 - Pietsch, K. A1 - Pöpping, B. A1 - Reiting, R. A1 - Schroeder, U. A1 - Schwägele, F. A1 - Weller, Michael G. A1 - Zagon, J. T1 - Methoden zur Differenzierung von Tierarten in Lebensmitteln – Status quo N2 - Nicht zuletzt bedingt durch den Pferdefleischskandal im Jahr 2013 wurden in Deutschland die Aktivitäten bei der Methodenstandardisierung im Bereich der Tierarten-Differenzierung in den vergangenen Jahren intensiviert. Wenn auch positive Befunde bei dem Nachweis von Bestandteilen aus Pferd in Lebensmitteln wie Lasagne derzeit so gut wie nicht mehr anzutreffen sind, so hat die Tierartendifferenzierung insgesamt beim Nachweis von Verfälschungen in Lebensmitteln einen hohen Stellenwert. Diese Arbeit fasst daher den aktuellen Stand der Analytik in Deutschland mit Schwerpunkt bei der Standardisierung zusammen. Sie wurde erstellt durch die Arbeitsgruppe „Biochemische und molekularbiologische Analytik“ der Lebensmittelchemischen Gesellschaft mit Unterstützung von Experten der Arbeitsgruppe „Molekularbiologische Methoden zur Pflanzen- und Tierartendifferenzierung“ (§ 64 LFGB) sowie der ALTS-Arbeitsgruppe „Immunologie und Molekularbiologie“ (jeweils D). KW - ELISA KW - PCR KW - Multiplex KW - DNA-Chip KW - Fischarten KW - Standardisierung KW - Molekularbiologie KW - Immunoassay KW - Hybridisierung KW - Digitale PCR KW - LC-MS/MS KW - Massenspektrometrie KW - Schnellmethoden KW - Screening KW - Milch KW - Microarray KW - LAMP KW - Laborvergleichuntersuchungen KW - Referenzmaterialien KW - Standardverfahren PY - 2017 SN - 0015-363X IS - 1 SP - 97 EP - 102 PB - Deutscher Fachverlag GmbH CY - Frankfurt AN - OPUS4-39038 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Waiblinger, H. U. A1 - Bartsch, D. A1 - Brockmeyer, J. A1 - Bruenen-Nieweler, C. A1 - Busch, U. A1 - Haase, I. A1 - Hahn, A. A1 - Haarmann, M. A1 - Hauser, W. A1 - Huber, I. A1 - Jany, K. D. A1 - Kirmse, N. A1 - Lindeke, S. A1 - Neumann, K. A1 - Naumann, H. A1 - Paschke, A. A1 - Pietsch, K. A1 - Pöpping, B. A1 - Reiting, R. A1 - Schroeder, U. A1 - Schwägele, F. A1 - Weller, Michael G. A1 - Zagon, J. T1 - Methods of differentiating animal species in foods – Status quo N2 - Work on standardising methods in the field of animal species differentiation has been intensified in Germany in recent years, not least due to the horsemeat scandal in 2013. Even though there are now hardly ever any positive findings any more in examinations to detect horse adulterations in foods such as lasagne, animal species differentiation altogether ranks high in detecting adulteration of foods. This article therefore summarises the current status of analytical techniques used in Germany with standardisation at German level. It has been established by the working group “Biochemical and Molecular Biological Analytics” of the Lebensmittelchemische Gesellschaft (Food Chemistry Society within the German Chemical Society) with support of experts in the working group “Molecular biology techniques for differentiating plant and animal species” (§ 64 of the German Food and Feed Code – LFGB) and the “Immunology and molecular biology” task force of the food hygiene and Food of animal origin working group (ALTS), both from Germany. KW - Animal species differentiation KW - Fish species KW - PCR KW - Standardisation KW - DNA chip KW - Multiplex methods KW - Digital PCR KW - ELISA methods KW - Immunoassays KW - LC-MS/MS KW - Reference materials KW - Microarrays KW - LAMP KW - Interlaboratory studies PY - 2017 SN - 0179-2415 VL - 97 IS - 1 SP - 50 EP - 55 PB - Deutscher Fachverlag GmbH CY - Frankfurt AN - OPUS4-39264 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Zutta Villate, J. M. A1 - Hahn, Marc Benjamin T1 - Radioactive gold nanoparticles for cancer treatment N2 - Dose enhancement by gold nanoparticles (AuNP) was shown to increase the biological effectiveness of radiation damage in biomolecules and tissue. Most of the current studies focus on external beam therapy on combination with AuNP. Here we present a Monte-Carlo study (Geant4) to characterise radioactive AuNP. Radioactive 198 Au emits beta and gamma rays and is considered for applications with solid tumours. To effectively apply 198 AuNP their energy deposit characteristics have to be determined in terms of intrinsic and extrinsic properties e.g. AuNP diameter, AuNP density, and their clustering behaviour. After each decay process, the energy deposit, inelastic scattering events, kinetic energy spectrum of secondary particles within the AuNP themselves and in a spherical target volume of water up to 1 μm radius were determined. Simulations were performed for AuNP radii ranging from 2.5 nm to 20 nm radius, different cluster sizes and densities. The results show an increase of the energy deposit in the vicinity of the AuNP up to 150 nm. This effect nearly vanishes for distances up to one micron. For the case of AuNP clusters and the same activity, the enhancement of the energy deposit increases with the relative gold mass percentage and therefore can be adjusted by changing AuNP radius or clustering behaviour. KW - Gold KW - Nanoparticle KW - Cancer KW - Monte-Carlo KW - Simulation KW - Cluster PY - 2019 DO - https://doi.org/10.1140/epjd/e2019-90707-x SN - 1434-6060 SN - 1434-6079 VL - 73 IS - 95 SP - 1 EP - 7 PB - Springer CY - Berlin AN - OPUS4-47964 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Zutta Villate, J. M. A1 - Viviana Rojas, J. A1 - Hahn, Marc Benjamin A1 - Anselmo Puerta, J. T1 - Synthesis of 198Au nanoparticles sub 10 nm due optimization on local dose by Monte Carlo simulations for cancer treatment N2 - To enhance the biological effects of radiation damage in cancerous cells, we present an alternative approach to the use of gold nanoparticles (AuNP), focusing on the synthesis and characterization of highly monodisperse, spherical radioactive gold nanoparticles 198AuNP. The size of the AuNP size was optimized with the help of Geant4/TOPAS particle scattering simulations, and energy deposition per nm3 per decay for varying radii (2–10 nm) was evaluated. This work is the foundation for ongoing experimental work to evaluate cell death induced by 198AuNP which aims for the use of radioactive gold nanoparticles in cancer treatment. KW - AuNP KW - Beta decay KW - Beta particle KW - Brachytherapy KW - Cancer treatment KW - Nanoparticles KW - Nanoparticle KW - DNA KW - DNA damage KW - Dosimetry KW - Energy deposit KW - Gamma ray KW - Geant4 KW - Geant4-DNA KW - Gold Nanoparticles KW - LEE KW - Low energy electrons KW - MCS KW - Microdosimetry KW - Monte-Carlo simulation KW - NP KW - Synthesis KW - TEM KW - OH radicals KW - Particle scattering KW - Radiation damage KW - Radiationtherapy KW - Radioactive decay KW - Radiolysis KW - Simulation KW - TOPAS KW - TOPAS-nbio PY - 2022 DO - https://doi.org/10.1007/s10967-022-08355-5 SN - 1588-2780 SP - 1 EP - 9 PB - Springer Nature AN - OPUS4-55132 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER -