Long-term storage of mouse spermatozoa after evaporative drying

To determine if mouse spermatozoa could be preserved long-term without using liquid nitrogen, mouse spermatozoa in trehalose-EGTA solution were partially evaporatively dried under nitrogen gas (5 min at flow rate10 l/min) and stored for 1 week and 5 months at 4, -20, and -80 degrees C before intracytoplasmic sperm injection. Fertilization rates were neither different with spermatozoa stored at 4, -20, or -80 degrees C for 1 week or 1, 3, and 5 months respectively, nor blastocyst formation rates with spermatozoa stored for 1 week and 1 month. However, spermatozoa stored at 4 and -20 degrees C for 3 months resulted in fewer blastocysts (35.1 and 54.3% respectively) when compared with spermatozoa stored at -80 degrees C (74.4%). Blastocyst formation rates using spermatozoa stored for 5 months at -20 degrees C (57.4%) or -80 degrees C (74.5%) were not significantly different from those stored for 3 months at the same temperatures respectively, but were significantly better than those stored for 5 months at 4 degrees C (10.2%). Blastocysts derived from spermatozoa stored for 3 and 5 months at -20 and -80 degrees C respectively, were then transferred to pseudopregnant mothers to develop into healthy liveborn offspring. No significant differences were found in embryo transfer rates (number of pups born/number of embryos transferred), weaning rates, or sex ratios of resultant pups, which were healthy and reproductively sound. These results demonstrate for the first time that partially evaporatively dried mouse spermatozoa in trehalose-EGTA solution can be preserved for long term at -20 and -80 degrees C. The possibility that the storage temperature must be less than the glass transition temperature is discussed.     

Photon absorption in a hybrid slurry photocatalytic reactor: Assessment of differential approximations

Radiative transfer inside a slurry photocatalytic reactor with hybrid illumination from both solar radiation and lamps is examined. The local volumetric rate of photon absorption is evaluated. For this purpose, the P1 and the modified differential approximations (MDAs) are used, and results compared to a solution by the Monte Carlo method. It is found that significant differences may arise between the predictions of the above approximations and the exact results provided by the Monte Carlo simulations. The P1 approximation is very inaccurate near to the radiation entrance for the partially collimated solar radiation, although it improves, as optical depth increases. As expected, the MDA improves the results near to the boundary. Surprisingly, it turns out to be much worse than the P1 approximation at medium and large optical depths. In the case of lamp irradiation, the behavior of the MDA is the opposite; it works better at small optical depths. © 2011 American Institute of Chemical Engineers AIChE J, 58: 3256–3265, 2012     

Deconvolution Combined with Digital Colocalization Analysis to Study the Spatial Distribution of Tight and Adherens Junction Proteins

The relative spatial distribution of proteins was investigated with immunofluorescent methods by confocal laser scanning microscopy and digital image restoration. For confocal data sets recorded with a voxel dimension of 50 × 50 × 150 nm noise and blur can be decreased and the resolution in the z-axis increased by applying the maximum likelihood estimation algorithm of the Huygens software. This approach was successfully applied to the study of tight and adherens junctions in relation to the actin cytoskeleton in Madin Darby Canine Kidney cells. Colocalization analysis was done for pairs of probes using a histogram-based method. F-actin, occludin, zonula occludens 1, and E-cadherin were included in the study. Double-labeled preparations were used. The combination of deconvolution with the colocalization of confocal data sets offers a powerful tool to investigate the spatial arrangement of proteins.     

A field survey of metal binding to metallothionein and other cytosolic ligands in liver of eels using an on-line isotope dilution method in combination with size exclusion (SE) high pressure liquid chromatography (HPLC) coupled to Inductively Coupled Plasma time-of-flight Mass Spectrometry (ICP-TOFMS)

The effect of metal exposure on the accumulation and cytosolic speciation of metals in livers of wild populations of European eel with special emphasis on metallothioneins (MT) was studied. Four sampling sites in Flanders showing different degrees of heavy metal contamination were selected for this purpose. An on-line isotope dilution method in combination with size exclusion (SE) high pressure liquid chromatography (HPLC) coupled to Inductively Coupled Plasma time-of-flight Mass Spectrometry (ICP-TOFMS) was used to study the cytosolic speciation of the metals. The distribution of the metals Cd, Cu, Ni, Pb and Zn among cytosolic fractions displayed strong differences. The cytosolic concentration of Cd, Ni and Pb increased proportionally with the total liver levels. However, the cytosolic concentrations of Cu and Zn only increased above a certain liver tissue threshold level. Cd, Cu and Zn, but not Pb and Ni, were largely associated with the MT pool in correspondence with the environmental exposure and liver tissue concentrations. Most of the Pb and Ni and a considerable fraction of Cu and Zn, but not Cd, were associated to High Molecular Weight (HMW) fractions. The relative importance of the Cu and Zn in the HMW fraction decreased with increasing contamination levels while the MT pool became progressively more important. The close relationship between the cytosolic metal load and the total MT levels or the metals bound on the MT pool indicates that the metals, rather than other stress factors, are the major factor determining MT induction.     

Emissions of DEHP‐free PVC flooring

Degrading 2‐ethylhexyl‐containing PVC floorings (eg DEHP‐PVC floorings) and adhesives emit 2‐ethylhexanol (2‐EH) in the indoor air. The danger of flooring degradation comes from exposing occupants to harmful phthalates plasticisers (eg DEHP), but not from 2‐EH as such. Since the EU banned the use of phthalates in sensitive applications, the market is shifting to use DEHP‐free and alternative types of plasticisers in PVC products. However, data on emissions from DEHP‐free PVC floorings are scarce. This study aimed at assessing the surface and bulk emissions of two DEHP‐free PVC floorings over three years. The floorings were glued on the screed layer of concrete casts at 75%, 85%, and 95% RH. The volatile organic compounds (VOCs) were actively sampled using FLEC (surface emissions) and micro‐chamber/thermal extractor (µ‐CTE, bulk emissions) onto Tenax TA adsorbents and analyzed with TD‐GC‐MS. 2‐EH, C9‐alcohols, and total volatile organic compound (TVOC) emissions are reported. Emissions at 75% and 85% RH were similar. As expected, the highest emissions occurred at 95% RH. 2‐EH emissions originated from the adhesive. Because the two DEHP‐free floorings tested emitted C9‐alcohols at all tested RH, it makes the detection of flooring degradation harder, particularly if the adhesive used does not emit 2‐EH.     

Comparing in situ particle monitoring to microscopic counts of plankton in a drinking water reservoir

In a one-year study, the multispecies assemblages of phytoplankton (picoplankton to microplankton) within a drinking water reservoir were counted, determined and evaluated in their size fractions using microscope enumeration (MC). The manual counts were compared with the size evaluation obtained by a light obscuring particle counter (PC) in order to evaluate its use for the monitoring practice of a drinking water reservoir. With this multispecies comparison we present a novel approach for the evaluation of automated counting systems.The picoplankton clearly remained uncounted by the PC even though its lower size limits imply an adequate match. The highest and most consistent count numbers of plankton (nano- and microplankton) and particles were obtained during the spring mass development. However, from the middle of the year onwards, the measured particle concentration surpassed the counted plankton abundances by two- to threefold indicating the rise of seston within the water column. This fraction would be missed if counted solely by MC. Further, the PC consistently undersized the biological counts, but not the minerogenic fraction represented by the manganese oxidising bacteria. Consequently, the rise and decline of Metallogenium bacteria was reliably monitored with the PC.The PC provides additional size information compared to other bulk optical sensors (turbidity, chlorophyll-a). The correlation of particles with probe measurement always exceeded the plankton coefficient, but all combinations of plankton, particle and probe measurement revealed significant linear regressions. However, the redundancy of the chlorophyll-a probes was also shown in order to explain plankton abundances.Our results indicate that background knowledge of the monitored system and cautious interpretation of data is required to allocate and understand automated particle counts. Therefore, only in combination with MC, the PC enables phytoplankton or minerogenic particle counts under frequent real-time monitoring conditions. As such it may serve as a helpful tool for example in critical situations in the management of drinking water reservoirs.     

Design of a multichannel, multiresolution smart imaging system

This paper presents the design of a multichannel imaging system where the different optical channels have a different angular resolution and field-of-view. Such an imaging system is able to resolve fine details in a small region of interest through the channel that has the highest angular resolution (0.0096°) while controlling the surrounding region through the channel that has the widest field-of-view (2×40°). An interesting feature of such a multichannel, multiresolution imaging system is that various image processing algorithms can be applied at different segments of the image sensor. We have designed a three channel imaging system where each optical channel consists of four aspheric lens surfaces. These three imaging channels share a single image sensor with a resolution of 1440×960 and a 10 μm pixel size. All imaging channels have diffraction-limited performance ensuring good overall image quality.     

Near-infrared spectroscopy for cocrystal screening. A comparative study with Raman spectroscopy

Near-infrared (NIR) spectroscopy is a well-established technique for solid-state analysis, providing fast, noninvasive measurements. The use of NIR spectroscopy for polymorph screening and the associated advantages have recently been demonstrated. The objective of this work was to evaluate the analytical potential of NIR spectroscopy for cocrystal screening using Raman spectroscopy as a comparative method. Indomethacin was used as the parent molecule, while saccharin and l-aspartic acid were chosen as guest molecules. Molar ratios of 1:1 for each system were subjected to two types of preparative methods. In the case of saccharin, liquid-assisted cogrinding as well as cocrystallization from solution resulted in a stable 1:1 cocrystalline phase termed IND-SAC cocrystal. For l-aspartic acid, the solution-based method resulted in a polymorphic transition of indomethacin into the metastable alpha form retained in a physical mixture with the guest molecule, while liquid-assisted cogrinding did not induce any changes in the crystal lattice. The good chemical peak selectivity of Raman spectroscopy allowed a straightforward interpretation of sample data by analyzing peak positions and comparing to those of pure references. In addition, Raman spectroscopy provided additional information on the crystal structure of the IND-SAC cocrystal. The broad spectral line shapes of NIR spectra make visual interpretation of the spectra difficult, and consequently, multivariate modeling by principal component analysis (PCA) was applied. Successful use of NIR/PCA was possible only through the inclusion of a set of reference mixtures of parent and guest molecules representing possible solid-state outcomes from the cocrystal screening. The practical hurdle related to the need for reference mixtures seems to restrict the applicability of NIR spectroscopy in cocrystal screening.