45 GHz frequency at 0.34 mW/cm<SU2</SU power density. The whole body specific absorption rate (SAR) was estimated to be 0.11 W/Kg. Exposure took place in a ventilated Plexiglas cage and kept
in anechoic chamber in a far field configuration from the horn antenna. After the completion of exposure period, rats were sacrificed and the whole brain tissue was dissected and used for study of double strand DNA compound inhibitor (Deoxyribonucleic acid) breaks by micro gel electrophoresis and the statistical analysis was carried out using comet assay (IV-2 version software). Thereafter, antioxidant enzymes and histone kinase estimation was also performed.
Results: A significant increase was observed in comet head (P < 0.002), tail length (P < 0.0002) and in tail movement (P < 0.0001) in exposed brain cells. An analysis of antioxidant enzymes glutathione peroxidase (P < 0.005), and superoxide dismutase (P < 0.006) showed a decrease while an increase in catalase (P < 0.006) phosphatase inhibitor library was observed. A significant decrease (P < 0.023) in histone kinase was also recorded in the exposed group as compared to the control (sham-exposed) ones. One-way analysis of variance (ANOVA) method was adopted for statistical
analysis.
Conclusion: The study concludes that the chronic exposure to these radiations may cause significant damage to brain, which may be an indication of possible tumour promotion (Behari and Paulraj 2007).”
“In this work we present a numerical investigation on the magnetic domain formation and magnetization reversal mechanism in submillimeter (250 mu m length) amorphous microwires with negative magnetostriction by means of micromagnetic calculations. The formation of circular magnetic domains surrounding an axially, multidomain-oriented central nucleus was observed for the micromagnetic GW4869 supplier model representing the amorphous microwire. The magnetization reversal described by micromagnetic computations is consistent
with a combined nucleation-propagation-rotational mechanism for the magnetization reversal after the saturated state. (C) 2011 American Institute of Physics. [doi:10.1063/1.3525564]“
“The hydrosilylation reactions of 5-viny1-2-norbomene with alpha,omega-bis(trimethylsiloxy)methylhydrosiloxane catalyzed by platinum hydrochloric acid (0.1M solution in tetrahydrofuran), Karstedt’s catalyst (Pt(2)[(VinSiMe(2))(2)O](3)) and platinum on the carbon have been studied. Dependence of reaction rate and active Si-H bonds’ conversion depth on the catalyst was investigated. Even in the excess of the 5-vinyl-2-norbomene, not all active Si-H groups participate in the hydrosilylation reaction. The reaction order, activation energies, and rate constants have been determined for hydrosilylation reactions in the presence of H(2)PtCl(6). The synthesized oligomers were characterized by Fourier transform infrared spectroscopy (FTIR),(1)H,(13)C, (1)H-(1)H correlation spectroscopy (COSY), and C,H-correlation NMR spectroscopy.