Gene/Protein Disease Symptom Drug Enzyme Compound
Pivot Concepts: Gene/Protein Disease Symptom Drug Enzyme Compound   Target Concepts: Gene/Protein Disease Symptom Drug Enzyme Compound

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Query: KEGG:D02259 (NaI)
1,823 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

Changes in readings of a NaI(Tl) monitor set on the surface of an ion exchange resin column used to purify primary coolant water at the Kyoto University Research Reactor were examined with mathematical models to clarify the radiological meanings. The concentration distributions of the nuclides in the interstitial water of the resin bed and those adsorbed on the resins were determined by use of the dispersion-convection theory coupled with the linear isotherm adsorption relation. The adsorbed amount that was assessed by this model was theoretically related to that made by a compartmental model. The buildup concentrations of nuclides in the core water and the decreased accompanying power operation and shut-down were modeled using the value representing the cleanup rate by the purification circuit. The values of this parameter were determined by the least squares method for observed concentrations of 24Na, a major radionuclide in the core water. Recognizing that the adsorption band had remained within the top 10 cm during the circulation of water through the column, the change in the amount of radionuclide adsorbed on the resin was calculated using a compartmental model. The amount of radionuclide adsorbed on the resin predicted by the model agreed well with the readings of the NaI(TI) monitor. Factors that affect the reading are discussed in relation to early detection of fuel defects.
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PMID:Radiological implications of readings with a NaI(Tl) monitor set on an ion exchange resin column for purifying primary coolant water. 796 Jul 85

Organotin intermediates for IVaraU synthesis were obtained following the reaction of 1-(2',3',5'-tri-O-toluyl-beta-D-arabinofuranosyl-5-iodouracil with (E)-1,2-bis(tri-(n-butyl) stannyl)ethene in the presence of catalytic (Ph3P)2PdCl2. A direct precursor for IVaraU, (E)-5-[2-tri-n-butylstannylvinyl]-arabinosyluridine, reacted with [123I]NaI (10 mCi) or alternatively [125I]NaI in the presence of methanol and chloramine T providing no-carrier-added (NCA) [123I]IVaraU in a radiolabeling yield up to 97%; the product was recovered following reversed phase HPLC. Unlabeled IVaraU was prepared in five steps from arabinosyluridine via an organotin intermediate with an overall yield of 22%. An exchange radioiodination was also identified, based on accessible BrVara U in the presence of water and a cuprous ion catalyst. [123I]NaI (up to 40 mCi) or alternatively [125I]NaI reacted under exchange conditions to give no-carrier-added [123,125I]IVaraU in a radiolabeling yield of 93%; the product was recovered following reversed phase HPLC.
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PMID:No-carrier-added [123I]1-(beta-D-arabinofuranosyl)-5(E)-(2- iodovinyl)uracil (IVaraU): high yield radiolabeling via organotin and exchange reactions. 806 61

We used a modified external gamma scanning technique to quantitate right and left lung permeability changes to iodinated sheep albumin before and after perilla ketone (PK)-mediated unilateral lung injury in seven anesthetized sheep. Three portable gamma scintillation probes containing 2-in. NaI crystals detected radioactivities of 51Cr-labeled red blood cells and 125I-labeled albumin over the right and left lungs and blood, respectively. Radioactivities were monitored for 1 h before and 3 h after infusion of 25 mg/kg PK into a single lung. Calculation of normalized slope index (NSI) (Roselli and Riddle, J. Appl. Physiol. 67: 2343-2350, 1989) over the 30-min interval before PK and over the 60- to 90-min interval after PK for each lung revealed a four- to five-fold NSI increase in lungs receiving PK (0.00237 +/- 0.00065 to 0.0109 +/- 0.0016 min-1) and no increase in contralateral control lungs (0.00214 +/- 0.00065 to 0.00201 +/- 0.00032 min-1). Observed changes in NSI were consistent with postmortem evaluations of each lung. Lungs receiving PK had significantly higher wet-to-dry lung weight ratios and extravascular lung water volumes than contralateral control lungs. Measured bloodless wet-to-dry lung weight ratios were 5.68 +/- 0.39 and 3.27 +/- 0.27 (P < 0.05) for PK and control lungs, respectively.
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PMID:Evaluation of perilla ketone-induced unilateral lung injury using external gamma scanning. 817 97

The benzodiazepine receptor tracer [123I]iomazenil (Ro 16-0154, IMZ) can be prepared in close to theoretical specific activity by the reaction of its tributyltin precursor (IMZ-SnBu3) with [123I]NaI in the presence of Iodogen. However, the labeling reaction is associated with variably high amounts of a volatile 123I byproduct. The purpose of these experiments was to characterize the volatile byproduct and to examine the effect on the course of the reaction of the following variables: solvent (MeOH, EtOH, HOAc, H2O), pH (2-7), oxidizing agent (chloramine-T, Iodogen, AcO2H), reaction temperature (22-128 degrees C) and structure of ArSnR3. The order of reactivity of oxidizing agents, at 22 degrees C for 30 min, was chloramine-T > Iodogen >> AcO2H. Raising the pH above 5.8 reduced the labeling, whereas raising the temperature increased the yield up to a maximum at 120 degrees (90%); at higher temperatures, decomposition occurred. The best conditions were 50 micrograms precursor, 50 microL 0.02 M chloramine-T; in aqueous HOAc (pH 3.3) at 120 degrees for 30 min. Variable amounts of volatile byproduct were observed for chloramine-T at different temperatures (2-21%) and for the three oxidizing agents at room temperature (3-22%). By contrast, the Bu3Sn derivatives of IBF, epidepride, beta-CIT and the Me3Sn derivative of beta-CIT gave high labeling yields with peracetic acid at room temperature, and < or = 2% volatile radioactivity. The volatile byproduct from the [123I]IMZ preparations was identified as I-[123I]iodobutane by its trapping characteristics and by its retention time in two different HPLC systems. Volatile activity was not generated in the absence of Bu3Sn precursor and was not due to the presence of impurities in the tributylstannyl precursor.
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PMID:Formation of 1-[123I]iodobutane in labeling [123I]iomazenil by iododestannylation: implications for the reaction mechanism. 828 59

Ten healthy males inhaled monodisperse Teflon particles (geometric diameter 3.6 microns, aerodynamic diameter 5.3 microns) labeled with 195Au (half-life 183 days). The leakage of 195Au from the particles in vitro in water was less than 0.2% per year. Retention over the thorax was followed for about 900 days using two separate detector systems. One system consisted of four Ge detectors placed close to the front of the chest over the upper and lower regions of the lungs. The other system consisted of three NaI crystals placed in a ring around the thorax at some distance from the chest wall. Activities of 195Au in feces (24- or 48-h samples) could be measured as long as activities in the thorax could be measured. For the period 7-250 days, the half-times were similar for the two detectors, on the average 740 days for the NaI detectors and 680 days for the Ge detectors. The average half-times estimated from measurements from about 250 days to about 900 days were 1750 days with the NaI detectors and 880 days with the Ge detectors. Clearance curves constructed from measurements from feces agreed very well with clearance measured with the NaI detectors. The excretion via feces was well described by a power function with days after exposure as base. This total clearance from the thoracic region was slower than in earlier studies. No activity could be measured in the urine. The measurements with the two detector systems show that a translocation within the thoracic region occurred. This might be explained by transportation of particles from the lung parenchyma to the regional lymph nodes. The accumulation of particles in the regional lymph nodes was tentatively calculated on the basis of that assumption.
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PMID:Long-term lung clearance of 195Au-labeled teflon particles in humans. 883 36

Fibers of the frog glossopharyngeal nerve that are sensitive to water stimulation also respond to Ca, Mg and Na salts. During stimulation with a salt, the cation and the anion are applied together and the anion could influence the response to the cation. We examined this interaction using single unit recordings at the level of fungiform papilla. Nerve impulses of large amplitude were recorded in response to the stimulation of adjacent papillae with increasing concentrations of various Ca, Mg and Na salts. For a given cation, the elicited spike frequency depended on the anion. For example, the responses of single fibers to Ca2+ concentrations above 0.1 mM were maximal with CaSO4 and minimal with Ca(SCN)2. The rank order of efficiency was CaSO4 > CaCl2 = CaBr2 = Ca(NO3)2 > Ca(SCN)2 for Ca2+ ions at 5 mM. The effects of these anions were reversed for Mg and Na salts, the rank orders being Mg(SCN)2 > Mg(NO3)2 > MgBr2 = MgCl2 > MgSO4, for Mg2+ ions at 200 mM, and NaSCN > NaI > NaNO3 > NaBr > NaCl >> NaF = Na2SO4, for Na+ ions at 500 mM. All these sequences correspond to the lyotropic rank order of the anions. In stimulation by a mixture of Ca and Na salts, which have different rank orders with respect to anions, either the response to Ca2+ ions or the response to Na+ ions could be eliminated as a result of mutual antagonism between Ca2+ and Na+ ions. In this case, the rank order of anions was dependent only on the cation that was able to exert a stimulatory effect in the mixture. Threshold concentrations for Ca, Mg and Na salts are influenced by cationic properties, but not by anionic properties. We hypothesize that anions can modulate the efficacy of cation transduction by binding to a membrane element that interacts with each of the three distinct receptors for Ca2+, Mg2+ and Na+ ions without altering the affinities of these receptors for the respective cations. The present results cannot be interpreted in terms of permeability of the apical membrane to anions and changes in surface potential on the apical membrane. The possibility is discussed that an anion-selective paracellular pathway between taste cells is responsible for the effect of anions on the cation-induced response.
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PMID:Anions modulate cation-induced responses of single units of the frog glossopharyngeal nerve. 897 52

A molecular model based in statistical thermodynamics is used to study salt effects on the lower consolute boundary of the aqueous non-ionic surfactant C8E5. The C8E5 micelles are modeled as hard spheres interacting via a temperature-dependent Yukawa attraction and the salt ions are modeled as positively and negatively charged hard spheres interacting via a Coulombic potential. The excess thermodynamic properties due to the Coulombic and Yukawa potentials are evaluated using the analytical solutions to the Ornstein-Zernike equation obtained for the mean spherical approximation closure. The Yukawa parameters for the micelle-micelle attractions are determined by fitting the theoretical phase diagram for a pure Yukawa fluid to the experimental lower consolute boundary for a salt-free C8E5 micelle-water solution. Ion-solvent interactions are indirectly accounted for by using previously determined adjusted values for the cation size and the dielectric constant of the medium. We evaluate theoretical coexistence curves for the C8E5 micelle-salt-water mixtures in the temperature-micelle volume fraction and temperature-salt molarity planes. We calculate the changes in the lower critical solution temperature (LCST) for the C8E5 micelle-salt-water mixture as a function of salt concentration for the salts NaF, NaCl, NaBr, NaI, and Na2SO4 and compare the trends seen with experiments. When ion-solvent interactions are indirectly accounted for, the theory correctly predicts the salting-out trends exhibited by NaF, NaCl, and NaBr. For the 1:2 salt (Na2SO4), charge effects resulting from the higher charge on the ions play a more important role in salting-out than ion-solvent interactions do. The theory, however, cannot predict the salting-in phenomena exhibited by NaI, thus indicating that salting-in is the result of variations in the intermicellar attraction as a function of the salt type and salt concentration. The theoretical results also indicate that excluded-volume forces resulting from the different sizes of the salt ions cannot alone account for the salting-in and salting-out phenomena seen in aqueous nonionic micellar solutions.
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PMID:The Effects of Salts on the Lower Consolute Boundary of a Nonionic Micellar Solution 897 49

The lateral absorbed dose, depth dose and photon fluence in a water phantom of a single microplanar beam is investigated using the Monte Carlo method. To validate the calculated axial and scattered photon fluence, an experiment is carried out using a NaI(TI) detector and 20 mCi Cd-109 source at energies of 22 keV and 88 keV. A 150 microns collimator is used to produce the microplanar beam, and the integrated scattered photon fluence is measured over 2.5 microns increments. The axial (depth) photon fluence is in good agreement with the calculated results. The scattered (lateral) photon fluence results agree to within two standard deviations.
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PMID:Measurements and Monte Carlo simulations of the fluence and dose characteristics of microplanar photon beams. 906 Feb 8

The construction, calibration and evaluation of a prompt- gamma in vivo neutron activation analysis (IVNAA) facility for the simultaneous measurement of total body nitrogen (TBN) and chlorine (TBCl) in children is described. Subjects are irradiated unilaterally by a 0.2 GBq 252Cf neutron source from shoulder to mid thigh in both supine and prone positions. Prompt gamma-ray spectra are measured with two pairs of NaI(TI) crystals (each crystal: 10 cm x 10 cm x 15 cm) positioned on both sides of the subject. TBN and TBCl are estimated from the ratios of nitrogen-to-hydrogen (Nc/Hc) and chlorine-to-hydrogen (Clc/Hc) counts as determined from the measurement of 10.83 MeV, 8.57 MeV and 2.22 MeV prompt gamma-rays from the respective reactions 14N(n, gamma)15N, 36Cl(n, gamma)35Cl, and 1H(n, gamma)D. Nc/Hc and Clc/Hc are corrected for the effect of body width and thickness on background and gamma-ray attenuation. Total body hydrogen (TBH) is used as an internal standard which is independently determined using a four compartment model of body weight defined as the sum of total body water (TBW) measured by the D2O dilution technique, total body protein (TBPr) (i.e. 6.25 x TBN) measured by IVNAA, total body bone mineral (TBBM) measured by dual energy x-ray absorptiometry and total body fat (TBF) estimated as body weight less the sum of TBW, TBPr and TBBM. The effective dose equivalent to a small child is 0.25 mSv (Q = 20) per measurement scan. Repeated measurements of a child-size bottle phantom containing tissue-equivalent concentrations of nitrogen and chlorine yield respective intra- and inter-assay precision values of 2.8% (CV) and 2.3% for TBN measurements, and 7.9% and 10.0% for TBCl measurements. Similarly, intra- and inter-assay accuracy is determined to be respectively +0.1% +/- 1.0% (mean, 95% confidence interval) and +1.4% +/- 1.4% for TBN measurements, and +2.3% +/- 4.3% and +3.9% +/- 6.0% for TBCl measurements.
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PMID:A neutron activation analysis facility for in vivo measurement of nitrogen and chlorine in children. 906 Feb 12

Rates of reaction of (+/-)-7beta,8alpha-dihydroxy-9alpha, 10alpha-epoxy-7,8,9,10-tetrahydrobenzo[a]pyrene (DE-2) have been determined in 1:9 dioxane-water solutions containing 1.0 M KCl, 0.5 M KBr, and 0.1 M NaI over the pH range 4-13. These pH-rate profiles are more complicated than those for reaction of DE-2 in 0.2 M NaClO4 solutions and are interpreted in part by mechanisms in which halide ion attacks the diol epoxide as a nucleophile at intermediate pH, resulting in the formation of a trans-halohydrin. Reaction of DE-2 in these halide solutions at pH < ca. 5 occurs by rate-limiting carbocation formation, followed by capture of the intermediate carbocation by halide ion. The relative magnitudes of the rate constants for reaction of the intermediate carbocation with halide ions are estimated from product studies. The halohydrins are unstable intermediates and react quickly in subsequent reactions to yield tetrols in a ratio different than that formed from reaction of the carbocation with solvent. Nucleophilic attacks of 1.0 M Cl-, 0.5 M Br-, and 0.1 M I- on DE-2 are the principal reactions in the pH range ca. 6-9, leading to intermediate trans-halohydrins that hydrolyze to tetrols. At pH ca. 9-11, halohydrin formed from attack of halide ion on DE-2 reverts back to epoxide, leading to a negative break in the pH-rate profile. The main product-forming reaction of DE-2 at pH 11.3 is the spontaneous reaction. At pH > 12, the rate of reaction of DE-2 increases due to a second-order reaction of HO- with DE-2.
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PMID:Halide effects in the hydrolysis reactions of (+/-)-7beta, 8alpha-dihydroxy-9alpha,10alpha-epoxy-7,8,9,10-tetrahydrobenzo- [a]pyrene. 962 31


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