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Increased tumour response of a murine fibrosarcoma to low temperature hyperthermia and low dose rate brachytherapy.

The present animal tumour study was carried out to determine the effectiveness of low temperature hyperthermia combined with low dose rate radiation based on the cell culture studies of our laboratory and others that demonstrated a significant radiosensitization obtained by low temperature hyperthermia and low dose rate radiation. Well-oxygenated murine fibrosarcoma Meth-A tumours growing in Balb/c mice were treated with heat (41 degrees C tumour temperature) by immersion of the tumour-bearing leg in a waterbath concurrently with low dose rate radiation. Radiation was delivered using 192Ir interstitial implantation at absolute dose rates of 0.416-0.542 Gy/h. The effect of heat alone on tumour growth and normal tissue was minimal. Tumour growth delay following 30 Gy radiation was 4.9 days. Significant delay in tumour growth was observed with the addition of low temperature hyperthermia delivered concurrently. Enhancement in radiation response was seen with increasing duration of heat treatment; tumour growth delays were 9.5 days following 4 h heat (41 degrees C) treatment and 16 days following 6 h treatment. Three sessions of fractionated hyperthermia 4 h/day during the course of low dose-rate radiation significantly delayed tumour growth to 18.6 days. The results indicate that fractionated heat treatment in conjunction with low dose rate radiation has potential for improving tumour response without adversely affecting normal tissue reaction. This in vivo study represents an extension of the cell culture data and provides further radiobiological basis for the combined use of low temperature hyperthermia and low dose rate radiation.

Animals↗
PubMed2002

Hygroscopicity of aerosol particles at low temperatures. 1. New low-temperature H-TDMA instrument: setup and first applications.

A hygroscopicity tandem differential mobility analyzer (H-TDMA) is described that allows a fast and accurate determination of the water uptake by submicrometer aerosol particles at temperatures below 0 degrees C. To avoid volatilization of semivolatile particles, the humidification works without heating the gas stream, and the gas-phase composition is not changed during the analysis. The applied scanning mobility analysis allows a fast and accurate measurement of the humidogram, but care has to be taken with too high scanning velocities leading to artifacts in the particle size measurement. During a field campaign at a high-alpine site (Jungfraujoch, 3580 m above sea level), humidograms of free tropospheric particles were measured at T= -10 degrees C. The hygroscopic growth of these particles was characterized by monomodal growth distributions, which means that in the observed size range (dry particle diameters (Do) = 50-250 nm) the free tropospheric aerosol was to a large extent internally mixed. No distinct deliquescence was observed, indicating that the multicomponent aerosol particles are present in a liquid state even at a low relative humidity (RH) <10%. At RH 85%, average hygroscopic growth factors of 1.44, 1.49, and 1.53 were measured for Do = 50, 100, and 250 nm. The estimated soluble volume fraction of the particles in the observed size range was found to be 0.79, 0.86, and 0.91, respectively.

Aerosols↗
PubMed2001

[Effective factors of flocculation-DAF pilot process treating water with low temperature and low turbidity from Miyun reservoir].

The hydraulic parameters in coagulation, flocculation and flotation units of DAF pilot process were systematically investigated when employing flocculants AS and PAC respectively. In general, the available parameters for PAC are more favorable in DAF process. For PAC as a flocculant during DAF run, the favorable coagulation rapid mixing time is 15 s, the flocculant mixing time is no less than 5 minutes. However for AS, the corresponding time values are greater than 30 s and more than 7.5 minutes respectively. The available coagulation mixing intensity is 300-1000 s-1. The available flocculation mixing intensity (average G) is 40-140 s-1, and the GT (average) value is greater than 2 x 10(4). Both equal-speed mixing and two or three stages mixing could provide slight better turbidity removal. For MJ model nozzle, the suitable recycle ratio is 5.0%-8.3% at dispersed pressure of 2.5-3.3 kg.cm2. The detention time and hydraulic intensity in contact zone of DAF tank have important effects on DAF turbidity removal.

Flocculation↗
PubMed1999

Room-temperature and low-temperature structure of Nd1-xCaxMnO3 (0.3 </= x </= 0.5).

The structure of the insulating manganites Nd(1-x)Ca(x)MnO(3) (0.3 </= x </= 0.5) has been studied against temperature using electron diffraction and neutron diffraction. At room temperature, the three compounds with x = 0.3, 0.4 and 0.5 exhibit the orthorhombic GdFeO(3)-type structure (a approximately 2(1/2)a(p), b approximately 2a(p), c approximately 2(1/2)a(p)). Below the charge-ordering temperature of approximately 250 K, a doubling of the lattice is observed along the a axis which could be interpreted as an ordering of the d(z(2)) Mn(3+) orbitals. The low-temperature polymorph has ortho-rhombic symmetry for x = 0.5 and monoclinic symmetry for x = 0.4 and 0.3. The low-temperature structure of the x = 0.4 sample was refined using neutron diffraction data. The HREM study at room temperature confirms the average GdFeO(3)-type structure and indicates the existence of defective areas with a lower symmetry.

Journal Article↗
PubMed2004

Development of a stabilized low temperature infrared absorption cell for use in low temperature and collisional cooling experiments.

We have constructed a stabilized low temperature infrared absorption cell cooled by an open cycle refrigerator, which can run with liquid nitrogen from 250 to 80K or with liquid helium from 80K to a few kelvin. Several CO infrared spectra were recorded at low temperature using a tunable diode laser spectrometer. These spectra were analyzed taking into account the detailed effects of collisions on the line profile when the pressure increases. We also recorded spectra at very low pressure to accurately model the diode laser emission. Spectra of the R(2) line in the fundamental band of 13CO cooled by collisions with helium buffer gas at 10.5K and at pressures near 1 Torr have been recorded. The He-pressure broadening parameter (gamma(0) = 0.3 cm(-1) atm(-1)) has been derived from the simultaneous analysis of four spectra at different pressures.

Argon↗
PubMed2005

Study of some Saccharomyces cerevisiae strains for winemaking after preadaptation at low temperatures.

Low-temperature fermentations (13 degrees C) are considered to improve wine aromatic profiles. However, because the risk of stuck and sluggish fermentations is high, these fermentations are not common. The aim of this paper was to analyze the effect of different preadaptation protocols in two commercial wine strains on the fermentation and some wine parameters. Preadaptation is understood to be the process between the rehydration of active dry yeast and the inoculation. In this study, it consisted of preparing a fermentation starter (addition of yeast grown at 25 degrees C) or inocula preadapted at low temperatures (as before, but grown at a fermentation temperature of 13 or 17 degrees C). These results were compared with those of rehydrated active dry yeast, and a commercial "cryotolerant" yeast was used as a reference. General fermentation kinetic parameters, yeast imposition, nitrogen consumption, and main wine products were analyzed. The results showed that the preadaptation of a yeast could improve the fermentation performance, although this improvement was strain-dependent. Low-temperature fermentations also had some general effects: reduction of acetic acid and fusel alcohol production and increased concentrations of glycerol. When the yeast performed better in fermentation because of preadaptation, nitrogen consumption was faster and the wine's "negative" attributes (acetic acid, fusel alcohols) were significantly reduced. Thus, in some strains, preadaptation could be an effective mechanism for improving low-temperature fermentation, which also significantly reduces detrimental wine attributes.

Adaptation, Physiological↗
PubMed2006

High-pressure freezing is a powerful tool for visualization of Schizosaccharomyces pombe cells: ultra-low temperature and low-voltage scanning electron microscopy and immunoelectron microscopy.

Yeast cells have a thick cell wall composed of an inner network of glucans and an outer layer of mannoproteins, which is difficult to penetrate with osmium tetroxide. We previously developed the sandwich technique to overcome this problem. Although the freeze-etching method allows the fracturing of cryofixed yeast cells, it has been difficult to fracture cryofixed yeast cells for examination by cryo-scanning electron microscopy (SEM). The development of an alternative method of cryofixation, namely, high-pressure freezing, began in the 1960s and is now available for the electron microscopic analysis of yeast. We show here that when high-pressure freezing is combined with ultra-low temperature and low-voltage SEM using the new cryo-system, the Gatan Alto 2500 Cryo Transfer System, fractured and coated yeast samples could be quickly prepared. These samples yielded a fine fracture plane and revealed the ultrastructure of both external and internal cell components. We used this method to analyze the process of septum formation, one of the final and most important events of mitosis, and cell separation. The images we obtained provide a three-dimensional view of these processes for the first time. We also showed that high-pressure freezing in combination with immunoelectron microscopy made it possible to preserve the antigenicity, in situ localization, and behavior of the cell wall component alpha-1,3-glucan and its synthase during septum formation in Schizosaccharomyces pombe.

Cell Cycle↗
PubMed1999

Trace rare gases optical emission spectroscopy: nonintrusive method for measuring electron temperatures in low-pressure, low-temperature plasmas.

Trace rare gases optical emission spectroscopy (TRG-OES) is a new, nonintrusive method for determining electron temperatures (T(e)) and, under some conditions, estimating electron densities (n(e)) in low-temperature, low-pressure plasmas. The method is based on a comparison of atomic emission intensities from trace amounts of rare gases (an equimixture of He, Ne, Ar, Kr, and Xe) added to the plasma, with intensities calculated from a model. For Maxwellian electron energy distribution functions (EEDFs), T(e) is determined from the best fit of theory to the experimental measurements. For non-Maxwellian EEDFs, T(e) derived from the best fit describes the high-energy tail of the EEDF. This method was reported previously, and was further developed and successfully applied to several laboratory and commercial plasma reactors. It has also been used in investigations of correlations between high-T(e) and plasma-induced damage to thin gate oxide layers. In this paper, we provide a refined mechanism for the method and include a detailed description of the generation of emission from the Paschen 2p manifold of rare gases both from the ground state and through metastable states, a theoretical model to calculate the number density of metastables (n(m)) of the rare gases, a practical procedure to compute T(e) from the ratios of experimental-to-theoretical intensity ratios, a way to determine the electron density (n(e)), a discussion of the range of sensitivity of TRG-OES to the EEDF, and an estimate of the accuracy of T(e). The values of T(e) obtained by TRG-OES in a transformer-coupled plasma reactor are compared with those obtained with a Langmuir probe for a wide range of pressures and powers. The differences in T(e) from the two methods are explained in terms of the EEDF dependence on pressure.

Journal Article↗
PubMed1989

Effects of salinity on the survival of non-O1 Vibrio cholerae under environments of low temperature.

Under low temperature conditions, the effects of survival and growth of non-O1 Vibrio cholerae were studied in laboratory microcosms. As the environmental factors, various concentrations of NaCl solution and that of mono- and bivalent cation added nutrient of polypeptone were used under several temperatures. The results of these experiments suggested an extended survival of non-O1 V. cholerae at low temperature. When a range of NaCl concentration in microcosms water was between 0.4% and 2.0% with absent of nutrient, the survival of this organism was good under the temperature from 10 degrees C to 20 degrees C. With added nutrient, when about 10 mM bivalent cation and over 0.3% NaCl co-existed, this strain was able to grow at 10 degrees C, and showed good survival. This finding suggested the possibility of survival under 10 degrees C.

Cold Temperature↗
PubMed2005

Identification of Low-temperature-regulated ORFs in the cyanobacterium Anabaena sp. strain PCC 7120: distinguishing the effects of low temperature from the effects of photosystem II excitation pressure.

Most organisms have developed various strategies to react rapidly to temperature down-shift and regulate expression of various genes to acclimate to low temperature. In photosynthetic organisms, temperature down-shift in the light results in not only a decrease in growth temperature but also an increase in PSII excitation pressure. Distinguishing the effects of low temperature from the effects of excitation pressure is necessary to understand the mechanism of low-temperature signal transduction. In this report, we analyzed changes in gene expression after three different environmental changes, i.e. temperature down-shift in the light, temperature down-shift in the dark and transfer to the dark, using DNA microarray in the cyanobacterium Anabaena sp. strain PCC 7120. By comparing the expression patterns under the three experimental conditions, we identified 15 open reading frames (ORFs) that were up-regulated by temperature down-shift both in the light and in the dark. These ORFs are considered to be regulated by low temperature, but not by excitation pressure. Six of them have a consensus sequence within the upstream region of their coding region and were indicated also to be up-regulated by tetracycline. Functional or structural changes in the ribosome could affect transcript levels of the low-temperature-regulated ORFs.

Anabaena↗
PubMed2001

Room-temperature monoclinic and low-temperature triclinic phase-transition structures of meso-octamethylcalix[4]pyrrole-dimethyl sulfoxide (1/1).

Crystals of the title complex, C28H36N4*C2H6OS, undergo a phase transition between room temperature and 198 K, as determined by X-ray diffraction techniques. A monoclinic form is observed at room temperature, while a triclinic modification is found at 198 K, with Z' changing from 1 to 2. Differential scanning calorimetry (DSC) of the calixpyrrole-dimethyl sulfoxide complex revealed a series of phase changes between 273 and 243 K. The transition from the room-temperature monoclinic form to the low-temperature triclinic form is reversible, as determined by changes in the cell dimensions from remeasuring selected reflections at room temperature and at temperatures below 223 K. The uncomplexed calix[4]pyrrole molecule shows no phase changes occurring between room temperature and 233 K, the low-temperature limit of the DSC.

Calorimetry, Differential Scanning↗