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1.
Phys Rev Lett ; 101(7): 072701, 2008 Aug 15.
Article in English | MEDLINE | ID: mdl-18764526

ABSTRACT

Reaction mechanism analyses performed with a 4pi detector for the systems 208Pb + Ge, 238U + Ni and 238U + Ge, combined with analyses of the associated reaction time distributions, provide us with evidence for nuclei with Z=120 and 124 living longer than 10(-18) s and arising from highly excited compound nuclei. By contrast, the neutron deficient nuclei with Z=114 possibly formed in 208Pb + Ge reactions have shorter lifetimes, close to or below the sensitivity limit of the experiment.

2.
Radiat Res ; 163(2): 222-31, 2005 Feb.
Article in English | MEDLINE | ID: mdl-15658899

ABSTRACT

TILDA, a new Monte Carlo track structure code for ions in gaseous water that is valid for both high-LET (approximately 10(4) keV/microm) and low-LET ions, is presented. It is specially designed for a comparison of the patterns of energy deposited by a large range of ions. Low-LET ions are described in a perturbative frame, whereas heavy ions with a very high stopping power are treated using the Lindhard local density approximation and the Russek and Meli statistical method. Ionization cross sections singly differential with energy compare well with the experiment. As an illustration of the non-perturbative interaction of high-LET ions, a comparison between the ion tracks of light and heavy ions with the same specific energy is presented (1.4 MeV/nucleon helium and uranium ions). The mean energy for ejected electrons was found to be approximately four times larger for uranium than for helium, leading to a much larger track radius in the first case. For electrons, except for the excitation cross sections that are deduced from experimental fits, cross sections are derived analytically. For any orientation of the target molecule, the code calculates multiple differential cross sections as a function of the ejection and scattering angles and of the energy transfer. The corresponding singly differential and total ionization cross sections are in good agreement with experimental data. The angular distribution of secondary electrons is shown to depend strongly on the orientation of the water molecule.


Subject(s)
Algorithms , Heavy Ions , Linear Energy Transfer , Models, Chemical , Radiometry/methods , Software , Water/chemistry , Computer Simulation , Models, Statistical , Monte Carlo Method , Radiation Dosage
3.
Radiat Res ; 157(2): 128-40, 2002 Feb.
Article in English | MEDLINE | ID: mdl-11835676

ABSTRACT

The large RBE (approximately 7) measured for the killing of Chinese hamster V79 cells by 340 eV ultrasoft X rays, which preferentially ionize the K shell of carbon atoms (Hervé du Penhoat et al., Radiat. Res. 151, 649-658, 1999), was used to investigate the location of sensitive sites for cell inactivation and the physical modes of action of radiation. The enhancement of the RBE above the carbon K-shell edge either may indicate a high intrinsic efficiency of carbon K-shell ionizations (due, for example, to a specific physical or chemical effect) or may be related to the preferential localization of these ionizations on the DNA. The second interpretation would indicate a strong local (within 3 nm) action of K-shell ionizations and consequently the importance of a direct mechanism for radiation lethality (without excluding an action in conjunction with an indirect component). To distinguish between these two hypotheses, the efficiencies of core ionizations in DNA atoms (phosphorus L-shell, carbon K-shell, and oxygen K-shell ionizations) to induce damages were investigated by measuring their capacities to produce DNA double-strand breaks (DSBs). The effect of photoionizations in isolated DNA was studied using pBS plasmids in a partially hydrated state. No enhancement of the efficiency of DSB induction by carbon K-shell ionizations compared to oxygen K-shell ionizations was found, supporting the hypothesis that it is the localization of these carbon K-shell events on DNA which gives to the 340 eV photons their high killing efficiency. In agreement with this interpretation, cell inactivation and DSB induction, which do not appear to be correlated when expressed in terms of yields per unit dose in the sample, exhibit a rather good correlation when expressed in terms of efficiencies per core event in the DNA. These results suggest that core ionizations in DNA, through core-hole relaxation in conjunction with localized effects of spatially correlated secondary and Auger electrons, may be the major critical events for cell inactivation, and that the resulting DSBs (or a constant fraction of these DSBs) may be a major class of unrepairable lesions.


Subject(s)
DNA Damage/radiation effects , DNA/radiation effects , Fibroblasts/radiation effects , X-Rays/adverse effects , Animals , Carbon/radiation effects , Cell Line/radiation effects , Cell Nucleus/radiation effects , Cell Survival/radiation effects , Cricetinae , Cricetulus , DNA, Bacterial/radiation effects , DNA, Recombinant/radiation effects , DNA, Single-Stranded/radiation effects , DNA, Superhelical/radiation effects , Dose-Response Relationship, Radiation , Electrons , Gamma Rays , Ions , Lung/cytology , Models, Biological , Oxygen/radiation effects , Phosphorus/radiation effects , Photons , Plasmids/radiation effects , Relative Biological Effectiveness
5.
Scand J Clin Lab Invest ; 54(6): 435-40, 1994 Oct.
Article in English | MEDLINE | ID: mdl-7809576

ABSTRACT

Based on results from the Belgian External Quality Assessment (EQA) Scheme, we studied the main factors affecting the between-laboratory variation of C-reactive protein determination. Participants using homogeneous systems with several calibration points generally achieved better performance. Working temperatures influenced the results to a lesser extent. The present study stresses the importance for EQA organizers to collect more detailed information about CRP analytical methods used by the participants. It also suggests that manufacturers should be more involved in the management of quality, in particular by striving for standardization of the material (kit and calibrator) they produce for CRP assay.


Subject(s)
C-Reactive Protein/analysis , Laboratories/standards , Belgium , Calibration , Fluorescence Polarization Immunoassay , Humans , Immunodiffusion , Nephelometry and Turbidimetry , Quality Control , Reproducibility of Results
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