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A directional spectrometer that uses a superheated emulsion of dichlorotetrafluoroethane at the centre of a 30 cm diameter moderating-sphere of nylon-6. The system has a telescope-design wherein the detector views a narrow solid angle of about 1/6 steradians. The hydrogenous sphere effectively attenuates laterally incident neutrons, thus providing a strong angular dependence of the response. The central detector is sequentially operated at seven temperatures between 25 and 55 degrees C in order to generate a matrix of nested response functions suitable for few-channel spectrometry. The response matrix of the system has been determined by calibrations with monoenergetic neutrons and by Monte Carlo neutron transport calculations. The double-differential unfolding method developed for this system applies the principle of maximum entropy and allows for the rigorous use of all a priori information. The spectrometer is intended for use in the mixed neutron/photon fields encountered in the nuclear power industry, being suitable for spatially distributed radiation sources with maximum neutron energies up to 10 MeV. 相似文献
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ML Nochomovitz AF Dimarco JT Mortimer NS Cherniack 《Canadian Metallurgical Quarterly》1983,127(3):325-329
We studied in 10 supine anesthetized dogs diaphragm contraction produced by electrical activation with intramuscular electrodes surgically implanted in the ventral surface of the diaphragm and compared this with activation of the ipsilateral phrenic nerve (C5, 6, and 7) before it entered the thorax. Repetitive 40-Hz pulse trains with supramaximal current stimulus were used after hyperventilation of the animals to apnea. A single intramuscular electrode within 1 to 2 cm of the site of phrenic nerve entry into the diaphragm produced a mean transdiaphragmatic pressure of 12.0 cm H2O +/- 0.97 SE and mean tidal volume of 0.27 L +/- 0.04 SE. Mean values observed with phrenic nerve stimulation were not statistically different, and both electrode systems produced equivalent outward abdominal motion and upper rib cage paradox, as monitored by inductive plethysmography. There was no difference in gas exchange during stimulation with a single hemidiaphragm electrode and mechanical ventilation compared at the same tidal volume and respiratory rate. Blockade of neuromuscular transmission with curare eliminated intramuscular and phrenic nerve stimulation proportionately, suggesting that activation of the diaphragm is dependent in both cases on the phrenic nerve. This technique does not entail manipulation of the phrenic nerve and may have clinical application as an alternative technique for diaphragm pacing. 相似文献
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A Golay I Hagon D Painot P Rouget AF Allaz Y Morel J Nicolet M Archinard 《Canadian Metallurgical Quarterly》1997,31(2):103-112
The ability of lonidamine (LND), an energolytic derivative of indazole-carboxylic acid, to modulate the cytotoxic activity of cisplatin (CDDP) and epidoxorubicin (EPI), singly or in combination, was investigated in two human breast cancer cell lines (MCF7 and T47D). A 72-hr post-incubation with a non-cytotoxic concentration of LND (75 microM) increased the activity of a 1-hr CDDP treatment as well as that of a 1 to 16-hr EPI treatment. A different pattern of interaction among the drugs and modulator was observed as a function of the sequence of drug treatment. Specifically, supra-additive or additive effects of the combination were obtained in the two cell lines according to the different treatment schemes. In particular, the maximum potentiation was observed in MCF7 cells simultaneously exposed to CDDP, EPI and LND for 1 hr and then post-incubated with LND for 72 hr, and in T47 first exposed to EPI and LND, then to CDDP and LND, and finally post-incubated with LND. Flow cytometric analysis of MCF7 cell distribution in the different cycle phases showed that combined treatment with EPI/CDDP/LND was able to stabilize cell cycle perturbations (mainly G2M accumulation) induced by individual agents. The ability of LND to potentiate CDDP and EPI cytotoxicity, and the consideration that LND causes side effects different from those caused by alkylating agents and anthracyclines, make this compound an attractive candidate for multidrug combination therapy in breast cancer. 相似文献
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