Compaction Characterisation of Paracetamol and Avicel Mixtures

Compression and stress relaxation data from powder mixtures of Avicel and paracetamol have been analysed using the David and Augsburger Maxwell model treatment and the Heckel, Kawakita and Shott equations. Scanning electron microscopy was further used to characterise the compacts. No direct relationship was found between the 1/k value of the Heckel plots, and the 1/B value of the Kawakita equations. However, the compaction mechanism of a material can be elucidated more readily if both methods are used together. The slope n of the Shott plot was shown to be a useful parameter for measuring the amount of stress relaxation and the rate of stress decay. The use of David & Augsburger's equation was limited to certain materials, which undergo Maxwell deformation. For binary system and those materials showing deviation from the David & Augsburger equation, a more sophisticated model is required for describing the deformation process.     

The digestion of monosaccharide residues of the cell walls of oat and vetch hays by rumen contents in vitro

The extent and pattern of digestion of oat hay (Avena sativa L.) and vetch hay (Vicia sativa L.) monosaccharides by rumen contents was studied in vitro. The ratios of matrix polysaccharides to lignin were 1.25:1 and 3.82:1 in the vetch and oat hays, respectively. Glucose, xylose and uronic acids were the main sugars in both plants, comprising about 90% of the total monosaccharides. Glucose, xylose and arabinose were mainly confined to the cell walls (CW), whereas galactose and uronic acids were found in high proportions in the soluble fraction. Vetch had a particularly high uronic acid content (14.4 g 100 g^?1 DM), of which 71% was pectic material. The ratios of CW-glucose to CW-xylose were 2.23:1 and 3.74:1 in the oat CW and vetch CW, respectively. Based on monosaccharide analyses of the CW material, it is suggested that the degree of branching of the matrix polysaccharides is about twice as high in vetch as in oat hay. Total glucose and xylose were more digestible in oat than in vetch hay, whereas most of the minor sugars and the total uronic acids were more digestible in the vetch. Irrespective of species, CW glucose was more digestible than CW xylose. The digestibilities of CW glucose, CW xylose and CW uronic acid were: 61.0, 55.3, 51.5, 34.3 and 62.7, 42.6 for the oat hay and vetch hay, respectively. Following the pattern of digestion, CW arabinose and CW glucose were digested faster than CW xylose and CW uronic acid, irrespective of plant species. The extent of digestion at 12 h of incubation of these sugars was higher in vetch than in oat hay. It is suggeted that the concentration ratio of rapidly to slowly degradable CW sugars, in a given plant, is a major determinant of the rate of CW digestion by rumen microorganisms.     

On wire-grid representation of solid metallic surfaces

This work deals with the wire-grid representation of metallic surfaces in numerical electromagnetic modeling. We discuss in particular the adequacy of the well known and widely used equal area rule (EAR) to calculate the radii of wire-grid models. We show that the EAR is accurate as long as the wire grid consists of a simple rectangular mesh. For more complex body-fitted meshes, using other polygons such as triangles, the EAR appears to be less accurate in reproducing the electromagnetic field scattered by metallic bodies. The conclusions of the paper are supported by numerical simulations performed using a parallel version of the numerical electromagnetics code and experimental data obtained on a vehicle illuminated by an electromagnetic pulse simulator.     

Comparison of the chronic toxicity of piroxantrone, losoxantrone and doxorubicin in spontaneously hypertensive rats

We have determined the time course, the spatial spread in brain tissue, and the intracellular distribution of biotin- and fluorescein-labeled phosphorothioate oligodeoxynucleotides (ODNs) following single injections into the rat striatum or the lateral ventricle. These time and space parameters were correlated with the ability of c-fos phosphorothioate antisense ODNs to suppress the induction of Fos protein by cocaine. A rapid and dose-dependent tissue penetration of labeled ODNs was observed following either intrastriatal or intraventricular injections of a constant sample volume. Inspection of tissue sections by confocal microscopy uncovered a distinct change in the intracellular disposition of labeled ODNs during the 24 h post-injection period. At 1, 6 and 12 h, the vast majority of the fluorescent signal was confined to the interstitial spaces throughout the zone penetrated by ODNs. Neuronal nuclei displayed faint labeling along the outer portion of the nucleus at 1 and 6 h post-injection. At these time-points, ODNs were not detected in the cytoplasm. By 16 h, ODNs were barely detectable in the extracellular space and absent from neuronal nuclei. Instead, ODNs were seen in large cytoplasmic granules of neurons throughout the tissue zone penetrated by the ODNs. Experiments with intrastriatal injections of antisense ODNs to c-fos mRNA revealed Fos suppression between 3 and 12 h, but not at 16 and 24 h. This combined analysis has revealed that (1) restricted tissue penetration by ODNs limits their antisense effects on protein expression, and (2) depletion of extracellular ODNs and sequestration of c-fos antisense ODNs into large intracellular granules coincides with the loss of their biological activity.     

Wounds from civilian and military centerfire rifles

To investigate the roles of astroglial cells, we targeted their ablation genetically. Transgenic mice were generated expressing herpes simplex virus thymidine kinase from the mouse glial fibrillary acidic protein (GFAP) promoter. In adult transgenic mice, 2 weeks of subcutaneous treatment with the antiviral agent ganciclovir preferentially ablated transgene-expressing, GFAP-positive glia from the jejunum and ileum, causing a fulminating and fatal jejuno-ileitis. This pathology was independent of bacterial overgrowth and was characterized by increased myeloperoxidase activity, moderate degeneration of myenteric neurons, and intraluminal hemorrhage. These findings demonstrate that enteric glia play an essential role in maintaining the integrity of the bowel and suggest that their loss or dysfunction may contribute to the cellular mechanisms of inflammatory bowel disease.     

Age-dependent inaccuracy of asthma death certification in Northern England, 1991-1992

OBJECTIVE: To test the usefulness of a commercial DNA hybridization assay for the detection of high-risk (HR) human papillomavirus (HPV) types in archival cervical smears and to compare the sensitivity with that of polymerase chain reaction (PCR) using consensus primers. STUDY DESIGN: Stained material was scraped from archival slides and the pellet volume noted. DNA was extracted using silica/guanidinium isothiocyanate and the quality checked by amplification of the beta-globin gene. HR-HPV DNA was detected using a commercial hybrid capture assay (HCA) and the results compared with an in-house amplification system with consensus primers. RESULTS: Of 156 archival smears stored for 12-13 years, 20 were positive by HCA using an HR probe cocktail. Ninety-eight were also tested by PCR, and 35 were positive. The percentage of HPV-positive samples increased with the increasing size of the pellet. HR-HCA detected more positives in samples with high grade squamous intraepithelial lesion (moderate/severe dyskaryosis). CONCLUSION: Both hybridization by HCA and amplification by PCR could be used to detect genital HPV in archival smears. The general primers PCR detected more positives than HR-HCA but included HPV 6/11. While variation in sample size and prolonged storage may reduce the quality of DNA, the use of archival material for longitudinal studies of HPV presence is potentially worthwhile.     

Phosphorylation of PITSLRE p110 isoforms accompanies their processing by caspases during Fas-mediated cell death

A number of cellular proteins have been identified as caspase targets during cell death, including the PITSLRE protein kinases. These targets generally fall into one of three possible categories: 1) other caspases, 2) proteins that are inactivated during apoptosis, and 3) proteins that are required for execution of the cell death program. However, not all proteins are cleaved by caspases during apoptosis. Why only specific proteins are destined to be processed by caspases during cell death is currently not clear. Here we show that multiple caspase-like activities are involved in the processing of the PITSLRE p110 isoforms during Fas-induced apoptosis in Jurkat T-cells. Three p110 caspase cleavage sites have been mapped to the amino-terminal domain of p110 and verified by site-directed mutagenesis. Curiously, the mutagenesis studies revealed that cleavage of two juxtaposed caspase sites is necessary for the complete processing of this protein during cell death in vivo. Finally, we demonstrate that the PITSLRE p110 protein is rapidly phosphorylated during Fas-induced apoptosis in Jurkat cells and that phosphorylation of an amino-terminal portion of the protein may enhance caspase cleavage in this region.