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- Gefahrgutverpackungen (2)
- Standard measurement procedure (2)
- Überdruck (2)
- Acquired immunodeficiency syndrome (1)
- Biofilms (1)
- CD4 expression level (1)
- CD4+ cell counting (1)
- Calibration (1)
- Dangerous goods packagings (1)
- Data loggers (1)
Organisationseinheit der BAM
This report focuses on the characterization of CD4 expression level in terms of equivalent number of reference fluorophores (ERF). Twelve different flow cytometer platforms across sixteen laboratories were utilized in this study. As a first step the participants were asked to calibrate the fluorescein isothiocyanate (FITC) channel of each flow cytometer using commercially available calibration standard consisting of five populations of microspheres. Each population had an assigned value of equivalent fluorescein fluorophores (EFF denotes a special case of the generic term ERF with FITC as the reference fluorophore). The EFF values were assigned at the National Institute of Standards and Technology (NIST). A surface-labelled lyophilized cell preparation was provided by the National Institute of Biological Standards and Control (NIBSC), using human peripheral blood mononuclear cells (PBMC) pre-labeled with a FITC conjugated anti-CD4 monoclonal antibody. Three PBMC sample vials, provided to each participant, were used for the CD4 expression analysis. The PBMC are purported to have a fixed number of surface CD4 receptors. On the basis of the microsphere calibration, the EFF value of the PBMC samples was measured to characterize the population average CD4 expression level of the PBMC preparations. Both the results of data analysis performed by each participant and the results of centralized analysis of all participants' raw data are reported. Centralized analysis gave a mean EFF value of 22,300 and an uncertainty of 750, corresponding to 3.3% (level of confidence 68%) of the mean EFF value. The next step will entail the measurement of the ERF values of the lyophilized PBMC stained with labels for other fluorescence channels. The ultimate goal is to show that lyophilized PBMC is a suitable biological reference cell material for multicolor flow cytometry and that it can be used to present multicolor flow cytometry measurements in terms of ABC (antibodies bound per cell) units.
A surface-labeled lyophilized lymphocyte (sLL) preparation has been developed using human peripheral blood mononuclear cells prelabeled with a fluorescein isothiocyanate conjugated anti-CD4 monoclonal antibody. The sLL preparation is intended to be used as a reference material for CD4+ cell counting including the development of higher order reference measurement procedures and has been evaluated in the pilot study CCQM-P102. This study was conducted across 16 laboratories from eight countries to assess the ability of participants to quantify the CD4+ cell count of this reference material and to document cross-laboratory variability plus associated measurement uncertainties. Twelve different flow cytometer platforms were evaluated using a standard protocol that included calibration beads used to obtain quantitative measurements of CD4+ T cell counts. There was good overall cross-platform and counting method agreement with a grand mean of the laboratory calculated means of (301.7 ± 4.9) µL-1 CD4+ cells. Excluding outliers, greater than 90% of participant data agreed within ±15%. A major contribution to variation of sLL CD4+ cell counts was tube to tube variation of the calibration beads, amounting to an uncertainty of 3.6%. Variation due to preparative steps equated to an uncertainty of 2.6%. There was no reduction in variability when data files were centrally reanalyzed. Remaining variation was attributed to instrument specific differences. CD4+ cell counts obtained in CCQM-P102 are in excellent agreement and show the robustness of both the measurements and the data analysis and hence the suitability of sLL as a reference material for interlaboratory comparisons and external quality assessment.
Microbial colonization affects the efficiency of photovoltaic panels in a tropical environment
(2015)
Sub-aerial biofilm (SAB) development on solar panels was studied in São Paulo. After 6, 12 and 18 months' exposure, photovoltaic panels were covered by increasing proportions of organic matter (42%, 53% and 58%, respectively). Fungi were an important component of these biofilms; very few phototrophs were found. Major microorganisms detected were melanised meristematic ascomycetes and pigmented bacterial genera Arthrobacter and Tetracoccus. While diverse algae, cyanobacteria and bacteria were identified in biofilms at 6 and 12 months, diversity at a later stage was reduced to that typical for SAB: the only fungal group detected in 18 month biofilm was the meristematic Dothideomycetes and the only phototrophs Ulothrix and Chlorella. Photovoltaic modules showed significant power reductions after 6, 12 (both 7%) and 18 (11%) months. The lack of difference in power reduction between 6 and 12 months reflects the dual nature of soiling, which can result from the deposition of particulates as well as from SAB fouling. Although 12-month old SAB demonstrated an almost 10-fold increase in fungal colonization and a higher organic content, the larger non-microbial particles (above 10 µm), which were important for efficiency reduction of lightly-biofilmed panels, were removed by high rainfall just before the 12-month sampling.
Rice is staple food of nearly half the world’s population. Rice yields must therefore increase to feed ever larger populations. By colonising rice and other plants, Herbaspirillum spp. stimulate plant growthand productivity. However the molecular factors involved are largely unknown. To further explore this interaction, the transcription profiles of Nipponbare rice roots inoculated with Herbaspirillum seropedicae were determined by RNA-seq. Mapping the 104 million reads against the Oryza sativa cv. Nipponbare genome produced 65 million unique mapped reads that represented 13,840 transcripts each with at least two-times coverage. About 7.4% (1,014) genes were differentially regulated and of these 255 changed expression levels more than two times. Several of the repressed genes encoded proteins related to plant defence (e.g. a putative probenazole inducible protein), plant disease resistance as well as enzymes involved in flavonoid and isoprenoid synthesis. Genes related to the synthesis and efflux of phytosiderophores (PS) and transport of PS-iron complexes were induced by the bacteria. These data suggest that the bacterium represses the rice defence system while concomitantly activating iron uptake. Transcripts of H. seropedicae were also detected amongst which transcripts of genes involved in nitrogen fixation, cell motility and cell wall synthesis were the most expressed.
The objective of this work was to determine the maximum gauge pressure in the vapour phase above the liquid in different design types of dangerous goods packagings under normal conditions of carriage. The design types investigated were steel and plastic packagings with a volume of approximately 6 l.
Two different methods were applied. In method 1, the pressure inside the packaging filled with a certain filling substance (dichloromethane) was directly measured under simulated conditions of carriage (degree of filling: 90%; filling temperature: 15°C; temperature during storage: 31°C). The maximum measured gauge pressures were between 89 mbar for a light plastic jerrican and 336 mbar for a steel drum.
In method 2, the gauge pressure was calculated. The consideration of a rigid packaging combined with the assumption of a vapour pressure of zero during filling and sealing can serve as a worst case scenario. The calculated gauge pressure is approximately 1061 mbar. This procedure leads to the highest safety factor and does not require any experimental investigations.
For a more realistic approximation of the gauge pressure of a non-rigid packaging, a packaging-specific function of relative expansion can be used, which is determined by a hydraulic pressure test. The calculated values ranged from 105 to 347 mbar. Method 2 provides conservative results. No hazardous filling substance is needed, and it allows a prediction of gauge pressure for other temperatures, substances and filling degrees. Therefore, this method could serve as alternative to UN Model Regulations 6.1.5.5.4 (a).
Der innere Überdruck, der sich unter Beförderungsbedingungen im freien Dampfraum einer Gefahrgutverpackung bildet, die mit einer gefährlichen Flüssigkeit gefüllt ist, hängt von verschiedenen Faktoren ab: Den spezifischen Stoffeigenschaften des jeweiligen Füllguts, dem Füllgrad, der Nachgiebigkeit der Verpackungsbauart, der Befülltemperatur und der Temperatur bei Beförderungsbedingungen.
Zu den normalen Beförderungsbedingungen von befüllten Gefahrgutverpackungen zählt der interkontinentale Transport in Frachtcontainern. Es werden die Ergebnisse einer Klimamessfahrt vorgestellt, die mit einem instrumentierten Frachtcontainer auf der Fahrt von Hamburg nach Singapur und zurück gewonnen wurden. Hierdurch lassen sich durchschnittliche und maximale Beförderungstemperaturen beim interkontinentalen Containertransport ermitteln. Es werden Modellgleichungen vorgestellt, mit denen sich für verschiedene Annahmen der sich einstellende Überdruck in einer Gefahrgutverpackung berechnen lässt.