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Carbon implantation is used to change the surface properties of materials without changing the bulk properties in various fields such as microelectronics, optics, tribology and biomaterials. While this implantation is usually performed at energies lower than 200 keV and thus in the low energy range of the stopping power curve, here we studied the effect of a 1 MeV ion beam which is in the medium energy range. The higher energies increase the modified depth range and thereby the load-carrying ability of metal surfaces. Light (Al), medium (Co) and heavy (W) metals were chosen as substrates. Three ion fluencies of 1016 ions/cm², 1017 ions/cm², and 1018 ions/cm² were used. Nuclear reaction analysis evidenced the presence of carbon at the samples surface and at a depth in accordance with Monte-Carlo (SRIM) simulations. Glancing incidence X-ray diffraction (GIXRD) allowed us to reveal the formation of aluminum carbide while no carbide was observed for Co and W. The modifications of the lattice parameters of Co and of W were studied by Rietveld refinements of X-ray diffraction patterns. For these metals the increase of the profile asymmetry of the diffraction peaks can result from the generation of dislocations induced by irradiation. The hardness measured by nano-indentation tests increases with the carbon ion dose, and the rise of hardness is larger for aluminum and tungsten than for cobalt.

A mononuclear iron(II) neutral complex (1) is screened for sensing abilities for a wide spectrum of chemicals and to evaluate the response function toward physical perturbation like temperature and mechanical stress. Interestingly, 1 precisely detects methanol among an alcohol series. The sensing process is visually detectable, fatigue-resistant, highly selective, and reusable. The sensing ability is attributed to molecular sieving and subsequent spin-state change of iron centers, after a crystal-to-crystal transformation.

We present newly reduced archival radio observations of SN 1996cr in the Circinus Galaxy from the Australia Telescope Compact Array and the Molonglo Observatory Synthesis Telescope, and attempt to model its radio light curves using recent hydrodynamical simulations of the interaction between the supernova (SN) ejecta and the circumstellar material (CSM) at X-ray wavelengths. The radio data within the first 1000 d show clear signs of free–free absorption (FFA), which decreases gradually and is minimal above 1.4 GHz after day ∼3000. Constraints on the FFA optical depth provide estimates of the CSM free electron density, which allows insight into the ionization of SN 1996cr's CSM and offers a test on the density distribution adopted by the hydrodynamical simulation. The intrinsic spectral index of the radiation shows evidence for spectral flattening, which is characterized by α = 0.852 ± 0.002 at day 3000 and a decay rate of Δα = −0.014 ± 0.001 yr−1. The striking similarity in the spectral flattening of SN 1987A, SN 1993J and SN 1996cr suggests this may be a relatively common feature of SNe/CSM shocks. We adopt this spectral index variation to model the synchrotron radio emission of the shock, and consider several scalings that relate the parameters of the hydrodynamical simulation to the magnetic field and electron distribution. The simulated light curves match the large-scale features of the observed light curves, but fail to match certain tightly constraining sections. This suggests that simple energy density scalings may not be able to account for the complexities of the true physical processes at work, or alternatively, that the parameters of the simulation require modification in order to accurately represent the surroundings of SN 1996cr.

We present archival radio observations of SN1996cr from ATCA and MOST, and model its radio lightcurves using X-ray constrained hydrodynamical simulations of the interaction between the SN ejecta and the CSM. The early radio data show signs of free-free absorption (FFA), which decreases gradually and is minimal above 1.4 GHz after day ~3000. FFA optical depth constraints provide estimates of the CSM free electron density, which allows insight into the ionisation of SN1996cr's CSM and offers a test on the density distribution adopted by the hydrodynamical simulation. The intrinsic spectral index of the radiation shows evidence for spectral flattening, which is characterised by alpha = 0.852 +/- 0.002 at day 3000 and a decay rate of d_alpha = -0.014 +/- 0.001 yr^-1. The similarity in the spectral flattening of SN1987A, SN1993J, and SN1996cr suggests this may be a relatively common feature of SNe/CSM shocks. We adopt this spectral index variation to model the synchrotron radio emission of the shock, and consider several scalings that relate the parameters of the hydrodynamical simulation to the magnetic field and electron distribution. The simulated light curves match the large-scale features of the observed light curves, but fail to match certain tightly constraining sections. This suggests that simple energy density scalings may not be able to account for the complexities of the true physical processes at work, or alternatively, that the parameters of the simulation require modification in order to accurately represent SN1996cr's CSM., Comment: 17 pages, 6 figures, 5 tables, accepted for publication in MNRAS

We present archival radio observations of SN1996cr from ATCA and MOST, and model its radio lightcurves using X-ray constrained hydrodynamical simulations of the interaction between the SN ejecta and the CSM. The early radio data show signs of free-free absorption (FFA), which decreases gradually and is minimal above 1.4 GHz after day ~3000. FFA optical depth constraints provide estimates of the CSM free electron density, which allows insight into the ionisation of SN1996cr's CSM and offers a test on the density distribution adopted by the hydrodynamical simulation. The intrinsic spectral index of the radiation shows evidence for spectral flattening, which is characterised by alpha = 0.852 +/- 0.002 at day 3000 and a decay rate of d_alpha = -0.014 +/- 0.001 yr^-1. The similarity in the spectral flattening of SN1987A, SN1993J, and SN1996cr suggests this may be a relatively common feature of SNe/CSM shocks. We adopt this spectral index variation to model the synchrotron radio emission of the shock, and consider several scalings that relate the parameters of the hydrodynamical simulation to the magnetic field and electron distribution. The simulated light curves match the large-scale features of the observed light curves, but fail to match certain tightly constraining sections. This suggests that simple energy density scalings may not be able to account for the complexities of the true physical processes at work, or alternatively, that the parameters of the simulation require modification in order to accurately represent SN1996cr's CSM., Comment: 17 pages, 6 figures, 5 tables, accepted for publication in MNRAS

The development of in vitro fertilisation (IVF) has created a new branch of medical science that has the potential to bring great happiness to those who achieve successful pregnancies and long periods of misery to those who are unsuccessful. As a part of some wider research into the support needs of clients, this paper addresses some of the challenges of managing patient satisfaction in an area of health sciences that is associated with high levels of patient uncertainty and also high aspiration for positive outcomes. The authors have used the literature of the business sector, especially retailing and marketing, to explore the key parameters of patient satisfaction and the outcomes have relevance for both medical practice and customer service.

PURPOSE: A pharmacokinetic study was carried out in rats to investigate the effect of arthritis on the glucuronidation of the nonsteroidal anti-inflammatory drug ketoprofen. METHODS: An i.v. bolus dose of R,S-ketoprofen (10 mg/kg) was administered to control (n = 6) and adjuvant-induced arthritic rats (n = 6). All experiments were carried out in bile-exteriorized animals. Concentrations of R- and S-ketoprofen in plasma, bile and urine, and of their glucuronides in bile and urine were determined by HPLC. In a separate series of experiments, the ex vivo plasma protein binding of R- and S-ketoprofen was measured in control and arthritic rats following i.v. administration of R,S-ketoprofen. RESULTS: As a result of a significant decrease in plasma albumin concentrations in arthritic rats, the unbound fraction of R- and S-ketoprofen was significantly increased (approximately 2-fold) in rats with adjuvant-induced arthritis. Total (i.e., bound plus unbound) plasma clearances of R- and S-ketoprofen were not different in arthritic rats. Unbound plasma clearances of both ketoprofen enantiomers, however, were significantly reduced (by 53% and 61%, respectively). This was due to a significant impairment in the formation of the R- and S-ketoprofen glucuronides. There was no apparent effect of adjuvant-induced arthritis on the chiral inversion of R- to S-ketoprofen. CONCLUSIONS: Adjuvant-induced arthritis in the rat leads to a significant impairment in the in vivo glucuronidation of R- and S-ketoprofen.

Recent studies support the hypothesis that non parenchymal cells (mainly macrophages) may play a role in the metabolism and cellular effects of paracetamol. In order to investigate this hypothesis, male Wistar rats were intravenously injected with either 7.5 mg/kg gadolinium chloride (Gd+) or NaCl 0.9% (Gd-). The treatment with GdCl3 decreased the number and the function of Kupffer cells in liver tissue, as assessed by the histological examination of the liver after colloidal carbon injection in the portal vein. Precision-cut liver slices (PCLS) were prepared from both groups of rats and cultured for 8h in Waymouth's medium in the presence and absence of 5 mM paracetamol. Interestingly, PCLS obtained from Gd+ rats exhibited a lower release of tumor necrosis factor (TNF-alpha) and a better viability than PCLS from control (Gd-) rats. Incubation with paracetamol led to a decreased glycogen level in liver slices from Gd+ or Gd-, without modifying neither liver morphology nor ATP level nor LDH release. A higher proportion of paracetamol glucuronide, was secreted from the slices obtained from Gd+ rats. These data suggest that Kupffer cells could affect the viability of PCLS in culture and are involved in the regulation of phase II metabolism in the adjacent hepatocytes. We propose that PCLS in culture is a suitable model to elucidate the biochemical mechanism underlying the modulation of metabolism occurring through hepatocytes-Kupffer cells interactions.

The effect of adjuvant-induced arthritis on hepatic microsomal glucuronidation was studied in the rat. Arthritis was induced by injection of Mycobacterium butyricum suspended in liquid paraffin. Vmax and the Michaelis-Menten constant values for the in vitro glucuronidation of R- and S-ketoprofen, acetaminophen, and diflunisal by liver microsomes obtained from control and adjuvant-induced arthritic rats were compared. In addition, uridine 5'-diphosphate-glucuronosyltransferase activity toward bilirubin and p-nitrophenol, as well as levels of cytochrome P-450 and beta-glucuronidase were determined in these microsomal preparations. Adjuvant-induced arthritis resulted in a significant reduction in hepatic cytochrome P-450 levels and in p-nitrophenol glucuronidation (5.65 +/- 0.40 versus 2.58 +/- 0.27 micromol.min/mg protein in control and arthritic rats, respectively, mean +/- S.E.M.). Glucuronidation of bilirubin and beta-glucuronidase activities in liver microsomes and in plasma were not affected by adjuvant-induced arthritis. Vmax (nmol/min/mg protein) for the formation of R-ketoprofen glucuronide, S-ketoprofen glucuronide, diflunisal phenolic glucuronide, and diflunisal acyl glucuronide was significantly decreased in arthritic rats (0.68 +/- 0.10, 0.77 +/- 0. 12, 0.044 +/- 0.005, 0.26 +/- 0.03, respectively) compared with control rats (1.45 +/- 0.04, 1.60 +/- 0.04, 0.087 +/- 0.008, 0.46 +/- 0.04, respectively). Glucuronidation of p-nitrophenol, ketoprofen and diflunisal, substrates which seem to be at least partly glucuronidated in the rat by isoenzymes of the UGT2B subfamily, was impaired in adjuvant-induced arthritis. Glucuronidation of bilirubin and acetaminophen, substrates of UGT1- isoenzymes, was not affected by adjuvant-induced arthritis. It seems, therefore, that adjuvant-induced arthritis in the rat leads to impaired glucuronidation of substrates of the UGT2B subfamily.

The formalin test was evaluated to assess the analgesic activity of diflunisal in the rat. Fifty microliters of a 5% formalin solution was injected into the hindpaw of rats and two distinct nociceptive behaviors, i.e. flinching/shaking and licking/biting of the injected paw, were recorded over 120 min. The effect of factors such as age of the animal, time of injection (morning vs. afternoon), site of injection (right vs. left hind paw) were evaluated. Both nociceptive behaviors exhibited a biphasic time course. Rats weighing 210-220 grams showed a more intense response compared to older rats weighing 240-250 or 270-280 grams. The nociceptive behavior response was affected by the time of formalin injection and was more pronounced in the morning. Diflunisal (100 mg/kg, i.v. infusion over 3 min) caused a significant delay in the flinching/shaking response vs. time curve, whereas the licking/biting response was significantly inhibited. When carried out under carefully controlled conditions, the formalin test may be useful to study the analgesic effect of diflunisal in the rat. It seems to be less sensitive, however, than other commonly used nociceptive tests.

info:eu-repo/semantics/published

info:eu-repo/semantics/published

info:eu-repo/semantics/published

info:eu-repo/semantics/published

info:eu-repo/semantics/published

info:eu-repo/semantics/published

Appartient à l’ensemble documentaire : RhoneAlp1, Avec mode texte

Appartient à l’ensemble documentaire : RhoneAlp1, Avec mode texte