Effect of oxalate test dose size on absolute and percent oxalate absorption

The purpose of this pilot study was to establish the dependence or independence of oxalate absorption on the quantity of the test dose of sodium oxalate over a range of test doses corresponding to physiological dietary oxalate intake values. Gastrointestinal oxalate absorption was measured with the [13C2]oxalate absorption test. Six healthy volunteers were always tested under standardized dietary conditions with 63 mg dietary oxalate and 800 mg dietary calcium per day. The volunteers were tested thrice each with sodium oxalate test doses of 25, 50, 200, and 600 mg. Additionally, 1000 mg sodium oxalate was applied once to three of these volunteers. The oxalate absorption of the six volunteers tested under the standardized conditions with 50 mg sodium [13C2]oxalate was 7.2 +/- 2.62 % (mean +/- SD), similar to the 120 volunteers tested previously: 8.0 +/- 4.4 % (mean +/- SD). The tests with sodium [13C2]oxalate doses in the range 25-1000 mg revealed similar percent oxalate absorption values. In conclusion, in healthy volunteers, the amount of oxalate absorbed in the gastrointestinal tract increased proportionally with the higher test doses of oxalate. However, percent oxalate absorption remained unchanged with test doses in the dose range of physiological dietary oxalate intakes.     

Effect of oxalate test dose size on absolute and percent oxalate absorption

The purpose of this pilot study was to establish the dependence or independence of oxalate absorption on the quantity of the test dose of sodium oxalate over a range of test doses corresponding to physiological dietary oxalate intake values. Gastrointestinal oxalate absorption was measured with the [¹³C₂]oxalate absorption test. Six healthy volunteers were always tested under standardized dietary conditions with 63 mg dietary oxalate and 800 mg dietary calcium per day. The volunteers were tested thrice each with sodium oxalate test doses of 25, 50, 200, and 600 mg. Additionally, 1000 mg sodium oxalate was applied once to three of these volunteers. The oxalate absorption of the six volunteers tested under the standardized conditions with 50 mg sodium [¹³C₂]oxalate was 7.2 ± 2.62 % (mean ± SD), similar to the 120 volunteers tested previously: 8.0 ± 4.4 % (mean ± SD). The tests with sodium [¹³C₂]oxalate doses in the range 25–1000 mg revealed similar percent oxalate absorption values. In conclusion, in healthy volunteers, the amount of oxalate absorbed in the gastrointestinal tract increased proportionally with the higher test doses of oxalate. However, percent oxalate absorption remained unchanged with test doses in the dose range of physiological dietary oxalate intakes.     

EPR and optical absorption spectra of VO2+ ions in calcium oxalate monohydrate single crystals

Abstract

Electron paramagnetic resonance (EPR) and Optical absorption spectra of vanadyl ions in calcium oxalate monohydrate single crystals have been studied. EPR spectrum at room temperature exhibits an isotropic octet spectrum. The detailed EPR analysis indicates that vanadyl ions exhibit liquid like behaviour. EPR spectrum has been studied at different temperatures. It is found that at 255 K, the EPR spectrum completely disappears. The optical absorption spectrum exhibits three absorption bands characteristic of vanadyl ions in tetragonal symmetry. From the optical data, the crystal field and tetragonal parameters have been evaluated.     

Assessment of intestinal absorption of trace metals in humans by means of stable isotopes

This study is aimed to demonstrate the feasibility of stable isotopes for the assessment of reliable data on fractional intestinal absorption of trace metals in healthy humans. Among the various methods available, the double isotope technique, i.e. one isotope given orally together with the test substance to be investigated and another isotope injected intravenously to correct for retention and endogenous excretion of the particular trace metal, provides quantitative figures of intestinal absorption at reasonable expenses with regard to costs for materials and number of samples to be evaluated. The trace metals exemplarily included in this study, i.e. iron, cobalt and molybdenum show diverging relations between absorbed fractions and amounts administered which are indicative for different regulatory mechanisms of their body content. Food ligands influence the fractional absorption significantly so that the uptake from a composite meal cannot be derived from results on uptake from particular foodstuffs. Therefore, validated data on the behaviour of intestinal absorption will significantly contribute to a better understanding of human trace metal metabolism.     

The vacuum ultraviolet absorption spectrum of diatomic calcium

Calcium granules (99.5%) have been heated to 615°C in a tantalum furnace and the absorption spectrum has been observed on the SA 61 beam line of SUFERACO (Orsay) using a 3-metre Balzers monochromator down to the -LiF cut-off (1015 Å). An intense Rydberg series has been observed between 1900 and 1500 Å. This series extends from n = 5 to n = 12 and gives the ionization potential at 63068 cm^?1 (1585.6 Å) or 7.819eV and the quantum defect δ = 1.73.     

Observation of pair absorption in calcium

Pair absorption has been observed in calcium using broad band absorption. The absorption peaks at the sum energy of the (4s4p) ¹P° and (4s3d) ¹D atomic states. A cross section of 1.3 × 10^-22 (P/A) cm² is measured corresponding to a reduced absorption coefficient of 1.3 × 10^-35 cm⁵. An error in earlier calculations predicting the reduced absorption coefficient for pair absorption in barium is noted. Simple scaling laws, our experimental results, and the assumption that the barium process is dominated by the resonant dipole-dipole interaction are used to deduce an upper limit for the calcium (4s3d) ¹D→(4s4p) ¹P° oscillator strength of 6.5 × 10^-4.     

The effect of gain and absorption on surface plasmons in metal nanoparticles

The compensation of loss in metal by gain in interfacing dielectric has been demonstrated in a mixture of aggregated silver nanoparticles and rhodamine 6G dye. An increase of the quality factor of surface plasmon (SP) resonance was evidenced by the sixfold enhancement of Rayleigh scattering. The compensation of plasmonic losses with gain enables a host of new applications for metallic nanostructures, including low- or no-loss negative-index metamaterials. We have also predicted and experimentally observed a suppression of SP resonance in metallic nanoparticles embedded in dielectric host with absorption. PACS 61.46.Df; 73.20.Mf; 78.67.Bf     

The perminvar effect and magnetic after-effect in magnesium manganese ferrite

An unstable perminvar effect was found in magnesium manganese ferrite at a temperature of –195°C and its connection with the magnetic after-effect was investigated. The analysis carried out on the basis of Néel's theory showed that both effects are a result of the same diffusion process. The experimental results also show that 180° Bloch walls are displaced when the sample is magnetized.

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- – 195° C qe, , . , - . , 180- .

     

服药前后草酸钙结石患者尿微晶的性质变化

采用X射线衍射(XRD)、傅里叶变换红外光谱(FTIR)、纳米粒度仪和透射电子显微镜(TEM)研究了6例草酸钙结石患者在服药前后尿微晶性质的变化.结果表明,服药后尿pH值由服药前的5.87±0.51增加至6.23±0.74;服药前的主要成分为尿酸、一水草酸钙(COM)和磷酸氢盐,服药后尿微晶种类和数量均比服药前减少;服药前,尿微晶的平均粒径为(579±326) nm,服药后减小至(404±338) nm;服药前尿微晶的Zeta电位为(-4.28±2.55) mV,服药后为(-7.29±4.16) mV,Zeta电位变负有利于防止尿微晶沉积;服药前尿微品棱角尖锐,有明显的团聚现象,而服药后尿微晶形貌圆钝,团聚较少.采用现代仪器分析研究服药前后草酸钙结石患者尿液微晶的性质变化,对临床上预防和治疗尿结石具有重要的临床意义.     

Infrared absorption spectrum of neutral magnesium donors in silicon

The infrared absorption spectrum of neutral magnesium donor impurities in silicon has been investigated under the high resolution of a Fourier-transform infrared spectrometer. The absorption spectrum measured at liquid helium temperature are observed to be clearly better than those reported earlier in the literature. Several new lines corresponding to excitation from ground state to higher excited states have been observed and identified.     

EPR and optical absorption study of Cr-doped ammonium oxalate monohydrate single crystals

The electron paramagnetic resonance (EPR) study of the Cr³⁺-doped ammonium oxalate monohydrate (AOM) single crystal is done at room temperature. Two magnetically inequivalent sites for chromium are observed. The hyperfine structure for Cr⁵³ isotope is also obtained. The spin Hamiltonian parameters are evaluated as: D=(309±2)×10⁻⁴ cm⁻¹, E=(103±2)×10⁻⁴ cm⁻¹, g=1.9820±0.0002, A=(161±2)×10⁻⁴ cm⁻¹ for site I and D=(309±2)×10⁻⁴ cm⁻¹, E=(103±2)×10⁻⁴ cm⁻¹, g=1.9791±0.0002, A=(160±2)×10⁻⁴ cm⁻¹ for site II, respectively. On the basis of EPR data the site symmetry of Cr³⁺ doped single crystal is discussed. The optical absorption spectra are recorded in 195-925 nm wavelength range at room temperature. The energy values of different orbital levels are determined. On the basis of EPR and optical data, the nature of bonding in the crystal is discussed. The values of different parameters are B=803, C=3531, D_q=2208 cm⁻¹, h=0.59 and k=0.21, where B and C are Racah parameters, D_q is crystal field parameter and h and k are nephelauxetic parameters, respectively.     

EPR and optical absorption studies of vanadyl impurity in lithium hydrogen oxalate single crystal

Electron paramagnetic resonance (EPR) and optical absorption studies of vanadyl ions in lithium hydrogen oxalate monohydrate single crystal and powder are reported at room temperature. Single crystal rotations in each of the three mutually orthogonal crystalline planes, $a{b}^1$, $b^1{c}^1$ and $a{c}^1$ indicate four different vanadyl complexes. The detailed investigation of EPR spectra indicates that one of the VO^{2 +} sites (the intense one) may enter the lattice substitutionally and the other three occupy the interstitial positions. From the angular variation, the spin Hamiltonian parameters are evaluated and discussed. The optical absorption spectrum shows four bands. From the optical and EPR data, various bonding parameters are determined and the nature of bonding in the crystal is discussed.     

超声对硫酸钙结晶过程影响的研究

研究了超声对硫酸钙结晶过程的影响。实验表明，与对比样相比，超声可以明显缩短成核时间，改变结晶量，影响结晶在不同方向的成长速度，使结晶的形状比例(长／宽)减小。粒度分布的定量测定和计算显示，超声使硫酸钙结晶粒度分布范围由200μm缩小到100μm，体积平均直径从69．9μm降到26．59μm；硫酸钙的成核速率提高2．74倍，但结晶成长速率减少到对比样的40．9％。两者番加的结果体现为结晶过程总速率的增加。     

The optical absorption of hydroxyl ions associated with divalent calcium in NaCl

The measurements confirmed the association of Ca²⁺ and OH^– in NaCl: CaCl₂ + NaOH, which causes an increase and a shift +0·031 of the OH^– absorption at 2·8, the extinction of the OH^– UV-absorption at 184 nm and the occurrence of new absorption bands between 160 and 210 nm.The measurements were performed at the II. Physikalisches Institut of the University of Stuttgart.     

Infrared absorption spectrum of singly ionized magnesium donors in silicon

The infrared absorption spectrum of singly ionized magnesium donor impurities in silicon has been measured. Due to better sample preparation and higher resolution of the instrument, the absorption spectrum obtained is much better than previous reports. Some new lines have been observed and identified. Besides the 2p_± line, the 3p_± line has also been observed for the first time to be a doublet indicating that the excited state np_± splits into two states due to chemical splitting.     

The effect of genuine pion absorption and emission on πd scattering

Intermediate pion absorption and reemission through π and ? rescattering has been included in a computation of πd elastic cross sections and polarizations for pion energies through the resonance region. Appreciable effects are computed for these observables, notably for polarizations.