Bibliothek

Notizen: Abstract: The effect of treatment with acute fluoxetine, a serotonin reuptake inhibitor, on the rate of serotonin synthesis in the rat brain was studied through autoradiography following intravenous administration of α-methyl-l-[3H]tryptophan. The rate of serotonin synthesis in fluoxetine-treated rats was compared with the rate measured in sham-treated rats (saline injection). Results showed a significant increase in the rate of synthesis in the majority of cerebral structures examined. The greatest increase (given as a percentage of rates in control animals) in the rate of serotonin synthesis was observed in the substantia nigra compacta (344%), hippocampus-CA3 (337%), dorsal hippocampus (283%), and caudate-putamen (232%). Fluoxetine had a less significant effect on the rate of synthesis in the pineal body (44%). Data suggest that acute fluoxetine treatment (30 mg/kg, i.p.) enhances the rate of serotonin synthesis in all the structures of rat brain examined in this work.

Notizen: Abstract: In vivo measurements by positron emission tomography of the brain serotonin synthesis rates in the normal dog, in the dog with increased plasma tryptophan concentration, and in the dog under different arterial oxygen tensions are described. The method described here permits repeated measurements in the same brain for the first time. An increase in the plasma tryptophan concentration from 16.6 to 191.5 and then to 381 μM resulted in close to a linear increase in the brain serotonin synthesis rate. When PaO2 was raised from 76 ± 2 to 106 ± 1 mm Hg, the rate of serotonin synthesis in the dog brain increased from 39 ± 8 to 54 ± 10 pmol g−1 min−1. The estimates of the Michaelis-Menten constants, Kappm and Vmax for the transport of tryptophan through the blood-brain barrier are 303 ± 54 μM and 63 ± 10 nmol g−1, min−1, respectively.

Notizen: We present a new method to evaluate the photo-oxidative activity of sunscreening agents based on the photodynamic oxidation of uric acid. Uric acid was selected as the oxidant probe for its high reactivity to singlet oxygen and oxygen radicals, high sensitivity of detection using electrochemical (EC) techniques, low light absorptivity and high photochemical stability in the UVA/B region of interest, and stability to autoxidation. The method is demonstrated by the photodynamic oxidation of uric acid on co-irradiation with Rose Bengal, a highly efficient photosensitizing dye for the production of singlet oxygen (1O2). Using this assay we found that the relative photodynamic oxidation rates of UVB-absorbing sunscreens in 80% methanol on irradiation with 〉290 nm light decreased in the order 2-ethylhexyl 4-dimethylaminobenzoate (DMABA-2EH) ≫ 2-ethylhexyl 4-methoxycinnamate (MCA-2EH) and the experimental sunscreens, 1-(1,1-dimethylethyl)-3-octanoyl-4,4-dimethyl- 1,4,5,6,-tetrahydropyridine (ICI-319) and 1-(2-methylpropyl)-3-propionyl-4,4-dimethyl-1,4,5,6-tetrahydropyridine (ICI-855). The relative photodynamic oxidation rates of UVA-absorbing sunscreens decreased in the order 4-tert-butyl-4'-methoxydibenzoylmethane (BMDBM) and 4-(2-propyl)benzophenone (PB) 〉 2-hydroxy-4'-methoxy-benzophenone (HMB) and 2,2'-dihydroxy-4-methoxybenzophenone (DHMB). We have confirmed the photodynamic activity of DMABA-2EH for the production of singlet oxygen (1O2) using electron paramagnetic resonance (EPR) spectroscopy and the reagent 2,2,6,6-tetramethyl-4-piperidone (4-oxo-TEMP). We failed to detect the photodynamic production of the oxyradicals, superoxide (O2.-) and hydroxyl radical (HO.) using N-tert-butyl-a-phenylnitrone (PBN) and 5,5-dimethyl-1-pyrrolidine-1-oxide (DMPO) as a result of photochemical interference caused by these spin-trapping reagents. The uric acid photo-oxidation assay was also used to compare the photodynamic reactivity of light-reflective, microfine oxides TiO2, ZnO and ZrO2 suspended in aqueous 80% methanol. All of the microfine oxides (uncoated) showed greater photodynamic reactivity in equimolar dispersion than did any of the organic UVA- and UVB-absorbing sunscreens in homogeneous solution. In this assay the photodynamic oxidation rates for the microfine oxides decreased in the order ZnO ≫ TiO2 (anatase) 〉 ZrO2 〉 TiO2 (rutile). Resume Nous presentons un nouveau procede d'evaluation de l'activite photooxydante d'agents pour ecrans solaires base sur l'oxydation photodynamique de l'acide urique. L'acide urique a ete choisi comme test a l'oxydation en raison de sa forte reactivite a l'oxygene singulet et aux radicaux oxygene, sa haute sensibilite a la detection par les techniques electrochimiques (EC), sa faible capacite d'absorption de la lumiere, sa stabilite photochimique elevee dans le domaine UVA/UVB concerne, et sa stabilite a l'autooxydation. La demonstration du procede est effectuee au travers de l'oxydation photodynamique de l'acide urique co-irradie avec du Rose du Bengale, colorant phosensibilisateur tres efficace pour generer de l'oxygene singulet (1O2). En mettant ce test en oeuvre nous avons trouve que les vitesses relatives d'oxydation photodynamique d'ecrans solaires aux UVB dans due methanol a 80%, irradies avec une lumiere 〉 290nm, diminuent dans l'ordre: 2-ethylhexyl 4-dimethylamino-benzoate (DMABA-2EH) ≫ 2-ethylhexyl 4-methoxycinnamate (MCA-2EH) et les ecrans a l'essai: la 1-(1,1-dimethylethyl)-3-octanoyl-4,4-dimethyl-1,4,5,6-tetrahydopyridine (ICI-319) et la 1-(2-methylpropyl)-3-propionyl-4,4-dimethyl-1,4,5,6-tetrahydropyridine (ICI-855). les vitesses relatives d'oxydation photodynamique d'ecrans solaires aux UVA diminuent dans l'ordre: 4-tert-butyl-4'-methoxydibenzoylmethane (BMDBM) et 4-(2-propyl) benzophenone (PB) 〉 2-hydroxy-4'-methoxybenzophenone (HMB) et 2'2'-dihydroxy-4-methoxybenzophenone (DHMB). Nous avons confirme l'activite photdynamique du DMABA-2EH pour la production d'oxygene singulet (1O2) en utilisant la spectroscopie par resonance paramagnetique electronique et le reactif 2,2,6,6-tetramethyl-4-piperidone (4-oxo-TEMP). Nous n'avons pas pu detecter la production photodynamique des oxyradicaux du superoxyde (O2.) et du radical hydroxyle (HO.) a l'aide de la N-ter-butyl-a- phenylnitrone (PBN) en raison d'interferences photochimiques causees par ces reactifs spin-Bloquants. Le test de photooxydation de l'acide urique a aussi ete utilise pour comparer la reactivite photodynamique d'oxydes microfins reflechisseurs de lumiere TiO2, ZnO et ZrO2 en suspension dans du methanol aqueux a 80%. Tous ces oxydes microfins (non enrobes) ont montre une meilleure reactivite photodynamique en dispersion equimolaire que ne l'a fait aucun des ecrans solaires aux UVA et UVB en solution homogene. Lors de ce test les vitesses d'oxydation photodynamique des oxydes microfins ont diminue dans l'ordre ZnO ≫ TiO2 (anatase) 〉 ZrO2 〉 TiO2 (rutile).

Notizen: The temperature dependence of the epitaxial growth of cerium dioxide (CeO2) layers on (111) silicon substrates was studied using ultra-high-vacuum evaporation, varying the substrate temperature in the range between 150 and 900 °C. Characterization using Rutherford backscattering spectrometry and reflection high-energy electron diffraction proved that a CeO2 layer on (111) silicon has considerably good crystalline quality in the range between 200 and 850 °C. It is clarified that the epitaxy can be attained even at surprisingly low temperatures (less than 200 °C). A substrate temperature above 850 °C leads to rather poor crystallinity due to an exponential increase of residual gas pressure. Refractive indices of the epitaxial layers were measured by ellipsometry to be in the range of 2.19–2.79.

Notizen: We demonstrate that surface-emitting lasers operating in an external cavity can produce high average powers, high peak powers, and ultrashort pulses. By optical pumping of InGaAs/InP multiple quantum well samples in an external cavity, we generated 190 mW both in continuous and mode-locked operation at 1.5 μm. Synchronous pumping at 100 MHz yielded 7.7 ps pulses with 15 mW average power. These were shortened to 1. 1 ps pulses with 64 W peak power by chirp compensation using diffraction gratings, and to 710 fs by negative group-velocity dispersion in an optical fiber.

Notizen: CeO2 layer was epitaxially grown for the first time on both (111) and (100) silicon substrates by vacuum evaporation. Characterization using Rutherford backscattering and reflection high-energy electron diffraction proved that a CeO2 layer on (111) Si has considerably good crystalline quality, whereas that on (100)Si contains a large amount of crystallographic defects, especially in the vicinity of the CeO2/Si interface. Auger electron spectroscopy analysis showed a uniform concentration distribution of Ce and O throughout the epitaxial layer.

Notizen: A new approach to dry etching of GaAs, digital etching, has been demonstrated. In digital etching, the etchant and an energetic beam, which induces chemical sputtering at the surface, alternately impinge onto the surface. Electrons and Cl2 gas were used as the energetic beam and the etchant, respectively, in the present experiment. Etching rates of 1/3 monolayer/cycle, independent of Cl2 flux and electron current density, were obtained. The present results show that an inherent self-limiting mechanism is involved and that the etching process is limited by the adsorption of etchant. This digital etching technique is expected to be applied to the fabrication of well-defined quantum wire and quantum box structures.

Notizen: A Mn–Zn ferrite with a grain size of about 2 μm has been developed for the transformer driven at around 1 MHz. The developed ferrite exhibits considerably lower core losses than a conventional Mn–Zn ferrite with a grain size of about 10 μm at a frequency of 0.5 to 2 MHz. The thin-type transformer using the developed ferrite driven at 1 MHz shows a high efficiency of more than 95% at an output power of 10 to 17 W and a much lower surface temperature rise than the transformer using the conventional ferrite. © 1998 American Institute of Physics.

Notizen: The electrical degradation of AlInAs/GaInAs high electron mobility transistor (HEMT) due to the fluorine contamination is quantitatively explained through the comprehensive annealing experiments and bias-temperature tests. The thermal degradation rate is found to be mainly determined by the following electrochemical reaction of fluorine with donor species after the quite fast diffusion of fluorine into the AlInAs layer. It is also confirmed that the thermal degradation is stringently affected by the electric field resulting in the one-sided degradation near the anode. These findings are valuable knowledges in improving the reliability of AlInAs/GaInAs HEMT under the dc accelerated life test at high temperature. © 1996 American Institute of Physics.