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Kostenkalkulation im Anlagenbau: Modell zur Bewertung der Konkurrenzfähigkeit im Entwicklungsstadium
(2020)
Während Grundchemikalien größtenteils im industriellen Maßstab mittels verfahrenstechnisch optimierter Großanlagen hergestellt werden, entwickeln Forschungsinstitute biobasierte Prozesse zur Herstellung von Plattformchemikalien im Labor- und Pilotmaßstab. Im Rahmen dieser Arbeit wird ein Kostenkalkulationsmodell zur Abschätzung der Investitions- und Betriebskosten verfahrenstechnischer Anlagen vorgestellt, auf dessen Basis die ökonomische Konkurrenzfähigkeit in der Entwicklung befindlicher Verfahren ermittelt werden kann. Das Modell ist fur Anwendungen im industriellen Maßstab
geeignet.
Hyperspectral imaging opens a wide field of applications. It is a well established technique in agriculture, medicine, mineralogy and many other fields. Most commercial hyperspectral sensors are able to record spectral information along one spatial dimension in a single acquisition. For the second spatial dimension a scan is required. Beside those systems there is a novel technique allowing to sense a two dimensional scene and its spectral information within one shot. This increases the speed of hyperspectral imaging, which is interesting for metrology tasks under rough environmental conditions. In this article we present a detailed characterization of such a snapshot sensor for later use in a snapshot full field chromatic confocal system. The sensor (Ximea MQ022HG-IM-SM5X5-NIR) is based on the so called snapshot mosaic technique, which offers 25 bands mapped to one so called macro pixel. The different bands are realized by a spatially repeating pattern of Fabry-Pèrot flters. Those filters are monolithically fabricated on the camera chip.
The critical process parameters cell density and viability during mammalian cell cultivation are assessed by UV/VIS spectroscopy in combination with multivariate data analytical methods. This direct optical detection technique uses a commercial optical probe to acquire spectra in a label-free way without signal enhancement. For the cultivation, an inverse cultivation protocol is applied, which simulates the exponential growth phase by exponentially replacing cells and metabolites of a growing Chinese hamster ovary cell batch with fresh medium. For the simulation of the death phase, a batch of growing cells is progressively replaced by a batch with completely starved cells. Thus, the most important parts of an industrial batch cultivation are easily imitated. The cell viability was determined by the well-established method partial least squares regression (PLS). To further improve process knowledge, the viability has been determined from the spectra based on a multivariate curve resolution (MCR) model. With this approach, the progress of the cultivations can be continuously monitored solely based on an UV/VIS sensor. Thus, the monitoring of critical process parameters is possible inline within a mammalian cell cultivation process, especially the viable cell density. In addition, the beginning of cell death can be detected by this method which allows us to determine the cell viability with acceptable error. The combination of inline UV/VIS spectroscopy with multivariate curve resolution generates additional process knowledge complementary to PLS and is considered a suitable process analytical tool for monitoring industrial cultivation processes.
Hypericin is one of the most efficient photosensitizers used in photodynamic tumor therapy (PDT). The reported treatments of this drug reach from antidepressive, antineoplastic, antitumor and antiviral activity. We show that hypericin can be optically detected down to a single molecule at ambient conditions. Hypericin can even be observed inside of a cancer cell, which implies that this drug can be directly used for advanced microscopy techniques (PALM, spt-PALM, or FLIM). Its photostability is large enough to obtain single molecule fluorescence, surface enhanced Raman spectra (SERS), fluorescence lifetime, antibunching, and blinking dynamics. Sudden spectral changes can be associated with a reorientation of the molecule on the particle surface. These properties of hypericin are very sensitive to the local environment. Comparison of DFT calculations with SERS spectra show that both the neutral and deprotonated form of hypericin can be observed on the single molecule and ensemble level.
Although integrins are responsible for the interaction of cells with their environment, e.g., the extracellular matrix or artificial substrates, there is still a lack of knowledge about their role in cell adhesion and migration on protein-coated substrates with microtopography. Understanding such interactions could lead to new applications in e.g., medical implants as well as shed light on processes such as embryonic development, angiogenesis, wound healing, and tumor progression. In this work, the influence of surface topography and chemistry on αvβ3 and α5β1 integrin-mediated cell adhesion and migration of healthy and malignant human cell types (human coronary artery endothelial cells, human osteosarcoma cells, and human skin fibroblasts cells) was studied, using microgrooved and flat substrates covered by two different extracellular proteins, fibronectin and vitronectin. Although some general behaviors can be observed, cell migration (speed, directionality, and persistence time) and morphological adaptation (cell area, aspect ratio, and circularity) of cells on protein coated microgrooved substrates are mainly dependent on the cell type and its specific integrin expression.
Cancer cells invade confined microchannels via a self-directed mesenchymal-to-amoeboid transition
(2019)
Cancer cell invasion through physical barriers in the extracellular matrix (ECM) requires a complex synergy of traction force against the ECM, mechanosensitive feedback, and subsequent cytoskeletal rearrangement. PDMS microchannels were used to investigate the transition from mesenchymal to amoeboid invasion in cancer cells. Migration was faster in narrow 3 μm-wide channels than in wider 10 μm channels, even in the absence of cell-binding ECM proteins. Cells permeating narrow channels exhibited blebbing and had smooth leading edge profiles, suggesting an ECM-induced transition from mesenchymal invasion to amoeboid invasion. Live cell labeling revealed a mechanosensing period in which the cell attempts mesenchymal-based migration, reorganizes its cytoskeleton, and proceeds using an amoeboid phenotype. Rho/ROCK (amoeboid) and Rac (mesenchymal) pathway inhibition revealed that amoeboid invasion through confined environments relies on both pathways in a time- and ECM dependent manner. This demonstrates that cancer cells can dynamically modify their invasion programming to navigate physically confining matrix conditions.
Melamine–formaldehyde (MF) resins are widely used as adhesives and finishing materials in the wood industry. During resin cure, either methylene ether or methylene bridges are formed, leading to the formation of a three‐dimensional resin network. Not only the curing degree, but also the chemical species present in the cured resin determine the quality of the final product. Analytical methods allowing a detailed investigation of network formation are of great benefit to manufacturers. In the present work, resin cure of an MF precondensate is studied at different temperatures (100–200 °C) without considering the initial pH as a factor. Isoconversional kinetic analysis based on exothermal curing enthalpies enables calculation of the crosslinking degree at a given time/temperature regime. A semiquantitative determination of the chemical groups present is performed based on solid‐state nuclear magnetic resonance data. Fourier transform infrared spectroscopy has shown to be a fast and reliable analytical tool with high sensitivity toward functional groups and with great potential for at‐line process control.
Hauptziel des Projektes war zum einen die Entwicklung einer validen Testmethode auf Grundlage vorliegender Normen, welche die in der betrieblichen Praxis auftretende Degradation abreinigbarer Filtermedien (hohe Temperaturen, aggressive chemische Atmosphären) praxisnah abbilden kann. Die Methode sollte auch die mechanische Alterung der Medien durch Staubbeaufschlagung sowie Abreinigungs Druckstöße berücksichtigen (DIN ISO 11057). Innerhalb des Projektes konnten umfangreiche Praxiserfahrungen mit der Inbetriebnahme und dem Betrieb einer schadgasbeaufschlagten, temperierbaren Testkammer zur chemischen Alterung von Filtermedien auf Grundlage der Vorgaben der DIN EN ISO 16891 gewonnen werden. Sollen vergleichbare Prüfdaten für mehrere Proben verlässlich ermittelt werden, sind bei den Untersuchungen demnach umfangreiche Randbedingungen zu beachten. Insbesondere zeigten die Untersuchungen den hohen technischen Aufwand zur Durchführung der Filtertests auf, welche nicht zuletzt auch aufgrund der erforderlichen Sicherheitstechnik und langen Untersuchungsdauer eine Umsetzung insbesondere bei KMU aus wirtschaftlichen Gründen erschwert ist. Es konnte weiter dargestellt werden, dass die Kombination von chemisch-thermischer und mechanisch(-thermischer) Alterung durch den Einsatz verschiedener Prüfeinrichtungen grundsätzlich umsetzbar ist. Die im Rahmen des Vorhabens entwickelte Testmethode einer chemischen Alterung der Filtermatrices durch Gasphasenexposition in einer Druckkammer ermöglicht kürzere Beanspruchungszeiträume bei reduziertem zu behandelnden Schadgasanfall und kann damit den wirtschaftlichen Betrieb eines entsprechenden Prüfstandes ermöglichen. Kombiniert mit der externen mechanischen Alterung durch Staubbeaufschlagung und Möglichkeit der parallelen Temperaturaufprägung gem. EN ISO 16891 auf mehrere Filtermedien-Proben lässt sich das thermisch, chemisch und mechanisch induzierte Degradationsverhalten von Filtermedien ggf. realitätsnah und mit wirtschaftlich vertretbarem Aufwand in eine Prüfvorschrift überführen. Entsprechende Validierungsarbeiten sind Bestandteil eines aktuell gestarteten Folgeprojektes. Das zweite Hauptziel des Projektes war es Ausrüstungen zu entwickeln, die zu einer verbesserten Beständigkeit gegenüber aggressiven Komponenten führen. Die Ergebnisse zeigten, dass mit dem Sol-Gelverfahren mechanisch stabile Beschichtungen auf Faservlies dauerhaft aufgetragen werden konnten, welche insbesondere die chemisch induzierte Degradation von Aramiden reduzieren können. Bei Aramiden handelt es sich um relativ teure Hochleistungsmaterialien, von welchen bekannt ist, dass ihre Beständigkeit sowohl gegen über UV-Strahlung als auch unterschiedlichen Schadgasen gering ist. Daher stellen die Beständigkeit der Materialien verbessernde Ausrüstungen eine wichtige Entwicklung für Unternehmen dar, um auf diese Weise beständigere Aramid-basierte Produkte zu erhalten. Als besonders geeignet stellten sich dabei Fluorcarbonausrüstungen, organisch-anorganische Hybride auf Basis von GPTMS und Zirkonium-haltige Ausrüstungen heraus.
The current paper studies the influence of geometrical parameters of the fused deposition modeling (FDM) - fused filament fabrication (FFF) 3D printing process on printed part strength for open source desktop 3D printers and the most popular material used for that purpose - i.e., polylactic acid (PLA). The study was conducted using a set of different nozzles (0.4, 0.6, and 0.8 mm) and a range of layer heights from the minimum to maximum physical limits of the machine. To assess print strength, a novel assessment method is proposed. A tubular sample is loaded in the weakest direction (across layers) in a three point bending fixture. Mesostructure evaluation through scanning electronic microscopy (SEM) scans of the samples was used to explain the obtained results. We detected a significant influence of geometric process parameters on sample mesostructure, and consequently, on sample strength.
So far, only few authors addressed the serum-free, defined differentiation of adipocytes. And there are hardly any trials available on the defined maintenance of adipocytes. In this study, the development of a defined culture medium for the adipogenic differentiation of primary human adipose-derived stem cells (ASCs) was aimed. Based on the addition of specific factors for the replacement of serum, ASCs were differentiated to viable and characteristic adipocytes for 14 days, which was proven through the accumulation of lipids, the expression of perilipin A and by the release of leptin and glycerol. Furthermore, a defined maintenance medium was developed, which supported the maturation and stability of cells for a long-term period of additional 42 days until day 56.