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PubMed2000

Radiosynthesis of [18F]Lu29-024: a potential PET ligand for brain imaging of the serotonergic 5-HT2 receptor.

In a previous work, Lu29-024 (2,5-dimethyl-3-(4-fluorophenyl)-1-(1-methyl-4-piperidinyl)-1H-indole), a selective 5-HT2A receptor antagonist with nanomolar affinity and high selectivity, was labeled with carbon-11 to evaluate its behavior as a potential PET ligand for the serotonergic 5-HT2A receptor in the central nervous system. Administration of this tracer to rats was followed by a good brain uptake, no brain labeled metabolites but no specific, regio-selective, binding at 20 and 40 min post injection. Despite this, the data noted at 20 and 40 min suggest that this tracer, if associated with a radioactive emitter with a longer half-life than that of carbon-11, could be useful for the quantification of 5HT2A receptors. For these reasons, we chose to label this compound, bearing a fluorine atom, with [18F]fluoride, in order to perform rat studies over a more prolonged time-scale. The precursor for the radiosynthesis of [18F]Lu29-024 was obtained in an overall yield of 20% by a multi-step synthesis including an acetonylation reaction followed by a Fisher indole reaction. The radiotracer was prepared by an aromatic substitution with activated [18F]fluoride followed by a decarbonylation reaction that employed Wilkinson's catalyst. The radiosynthesis of [18F]Lu29-024 required approximatively 110 min with an overall radiochemical yield of 20-35% and specific activities of 37GBq/micromol. Fluorine-labeled Lu29-024 may thus be envisaged as a potentially useful PET tracer that can be applied to a wide range of neurological and psychiatric diseases.

Animals↗
PubMed2001

Separation of critical radioactive and non-radioactive species from aqueous waste streams.

The separation of radioactive and non-radioactive species from the simulated DOE neutralized current acid waste (NCAW) stream was studied. Cation and anion species were referred to their possible basic compounds, and divided into seven groups (nitrate, phosphate, sulfate, fluoride, nitrite, carbonate, and hydroxide). The nitrate group (the major anion in the DOE waste streams) contains several cations species, while the rest of the groups are only in the form of sodium. The precipitation measurements were conducted in three experimental stages. In the first stage, the precipitation of sodium sulfate, sodium phosphate, sodium-sulfate-phosphate, and aluminum nitrate systems were studied using isopropylamine (IPA) as a precipitation solvent. The objectives of this stage were to evaluate the precipitation ability of IPA in precipitating these compounds individually, and to validate the consistency of the analytical instruments and the employed experimental procedure. Tests performed on the acquired data indicated a high level of experimental consistency. The removal of phosphate, sulfate and aluminum were very high. In the second stage, the precipitation studies were conducted on the: (1) nitrate group alone; (2) binary groups containing the groups of nitrate-phosphate, nitrate-sulfate, nitrate-fluoride, nitrate-nitrite, and nitrate-carbonate; (3) combined nitrate, phosphate, sulfate, and fluoride groups and (4) combined nitrate, phosphate, sulfate, fluoride, nitrite, and carbonate groups. IPA was used as a precipitation solvent. The objectives of this stage were to evaluate the interactions of these groups in the absence of the hydroxide group (e.g. DOE acid-dissolved sludge and acidified supernate streams), and the influence of such interactions on the individual removal of the targeted species. The removal of the aluminum, phosphate, fluoride, and alkaline cations were significantly high (reached 99.9%). The removal of sulfate were moderately high (reached 87%), and the removal of nitrate and alkali cations including cesium were to some extent low (reached about 50%). In the third stage, the precipitation of inorganic species from the simulated NCAW stream was studied using IPA and ethylamine (EA). The precipitation process is very feasible for reducing the radioactivity contents of alkaline cations. However, the process is less effective in separating alkali cations including cesium. The removal of polyvalent transition metals such as aluminum ion is negatively influenced by the significant presence of hydroxide. While the process is effectively capable of separating phosphate, fluoride, and sulfate, it is significantly less effective in separating nitrate and nitrite. A previously derived thermodynamics framework was used to model the precipitation measurements. The framework provided two predictive equations (the 2-Suffix and 3-Suffix equations). Both equations were reasonably adequate for predicting the solubility phase behavior of tested inorganic species in a mixed-solvents mixture as well as for estimating optimum interaction parameters. However, the 3-Suffix equation was better than the 2-Suffix equation. The parameters were useful for estimating the: (1) precipitation fractions (%P) of the studied species, for instance, at different concentration levels of similar targeted species, or in different waste streams with similar or approximate abundance of species, or at different solvents volume ratio (V(r)) where no experimental data are available.

Chemical Precipitation↗
PubMed1980

Percutaneous absorption of carbon 14 labeled insect repellents in hairless dogs.

The percutaneous penetration of three insect repellents was determined in hairless dogs. Each compound was administered intravenously and topically to three dogs. Urine, feces and blood samples were assayed for radioactivity by scintillation counting. The percent penetration for N,N-diethyl-m-toluamide (m-deet, the most widely used insect repellent), its isomer N,N-diethyl-p-toluamide and 2-ethyl-1,3-hexanediol were 7.9%, 7.6%, and 10.3% respectively. The results for m-deet penetration in the hairless dog are comparable to those in man.

Administration, Topical↗
PubMed1995

Synthesis of 5-HT3 receptor antagonists, [11C]Y-25130 and [11C]YM060.

Two high-affinity 5-HT3 receptor ligands, Y-25130 and YM 060, have been labeled with 11C for use in PET studies to measure 5-HT3 receptors. The [11C]Y-25130 was prepared by N-methylation of nor-Y-25130-BH3 complex with [11C]CH3I in the presence of K2CO3 followed by HCl hydrolysis. Likewise, N-methylation of nor-YM060 gave [11C]YM060. After HPLC separation, the decay-corrected radiochemical yield of the two 11C-labeled ligands was 34-40% based on [11C]CH3I, the specific activity was 10-12 GBq/mumol at 35-40 min from EOB, and the radiochemical and chemical purities were > 99%. In mice, the brain uptake of the two compounds was the lowest among the tissues investigated, but the level of the brain radioactivity increased with time.

Animals↗
PubMed1973

Diazoacetyl subtilisin.

Subtilisin reacts at pH 6.8-7.8 with p-nitrophenyl diazoacetate to release p-nitrophenol and form diazoacetyl subtilisin. Although at pH 7.8 this derivative rapidly undergoes hydrolytic cleavage to regenerate active enzyme, the derivative can be trapped by rapidly lowering the pH to 5. Similarly, with (14)C-labeled p-nitrophenyl diazoacetate, the corresponding radiochemically labeled diazoacetyl enzyme can be prepared. Photolysis of this radioactive derivative incorporates radioactivity into the protein, and subsquent hydrolysis gives rise to several radioactive components, which, however, have not yet been identified.

Acetates↗
PubMed2003

Assessment of radioactive residues arising from radiolabel instability in a multiple dose tissue distribution study in rats.

Our study objectives were: To quantitatively determine the effect of radiolabel instability on terminal phase radioactive tissue residues in a multiple dose tissue distribution study. To quantitatively compare tissue residue artifacts (non drug-related radioactivity) from two chemically-distinct radiolabel locations. To conduct a definitive multiple dose tissue distribution study using the better of the two radiolabeled compounds. We compared the excretion and tissue distribution in rats of [(14)C]linezolid, radiolabeled in two different locations, after 7 consecutive once daily [(14)C] oral doses. The radiolabels were in the acetamide (two carbon) and oxazolidinone (isolated carbon) functional groups. Terminal phase tissue residue and excretion data were compared to data from rats dosed orally with [(14)C]sodium acetate. Drug-related radioactivity was excreted rapidly over 24 h. After a single dose, the acetamide and oxazolidinone radiolabel sites both gave 3% of dose as exhaled (14)CO(2). After 7 daily [(14)C] oral doses, terminal phase radioactive tissue residues were higher from the acetamide radiolabel, relative to the oxazolidinone radiolabel, and were primarily not drug-related. In the definitive tissue distribution study, low concentrations of drug-related radioactivity in skin and thyroid were observed. We conclude that although small amounts of radiolabel instability do not significantly affect single dose tissue radioactivity C(max) and AUC, artifacts arising from radiolabel instability can prolong the apparent terminal phase half life and complicate study data interpretation. When possible, it is always preferable to use a completely stable radiolabel site.

Acetamides↗
PubMed1980

Production of methanol from aromatic acids by Pseudomonas putida.

When grown at the expense of 3,4,5-trimethoxybenzoic acid, a strain of Pseudomonas putida oxidized this compound and also 3,5-dimethoxy-4-hydroxybenzoic (syringic) and 3,4-dihydroxy-5-methoxybenzoic (3-O-methylgallic) acids; but other hydroxy- or methoxy-benzoic acids were oxidized slowly or not at all. Radioactivity appeared exclusively in carbon dioxide when cells were incubated with [4-methoxyl-14C]trimethoxybenzoic acid, but was found mainly in methanol when[methoxyl-14C]3-O-methylgallic acid was metabolized. The identity of methanol was proved by analyzing the product from [methoxyl-13C]3-O-methylgallic acid by nuclear magnetic resonance spectroscopy and by isolating the labeled 3,5-dinitrobenzoic acid methyl ester, which was examined by mass spectrometry. These results, together with measurements of oxygen consumed in demethylations catalyzed by cell extracts, showed that two methoxyl groups of 3,4,5-trimethoxybenzoate and one of syringate were oxidized to give carbon dioxide and 3-O-methylgallate. This was then metabolized to pyruvate; the other product was presumed to be the 4-methyl ester of oxalacetic acid, for which cell extracts contained an inducible, specific esterase. P. putida did not metabolize the methanol released from this compound by hydrolysis. Support for the proposed reaction sequence was obtained by isolating mutants which, although able to convert 3,4,5-trimethoxybenzoic acid into 3-O-methylgallic acid, were unable to use either compound for growth.

Enzyme Induction↗
PubMed1985

Measures of de novo synthesis of milk components from propionate in lactating goats.

Possible direct contributions of propionate to de novo synthesis of milk components by the mammary gland of lactating goats fed a concentrate-roughage diet have been studied in vivo by primed constant infusion of [1-carbon-14]propionate into the right mammary artery. Specific radioactivities of milk galactose, fatty acids, and protein were higher in the infused than in the uninfused half of the mammary gland, suggesting de novo synthesis of these compounds in the udder. Specific radioactivities of milk glucose in both udder halves were identical, ruling out any possibility of mammary gland-derived glucose from propionate of blood plasma under the experimental conditions. Of milk galactose, .8% was derived from propionate of blood plasma, and of milk glucose, 98% was derived from glucose of blood plasma. After intraruminal infusion of unlabeled propionic acid at 11 g/h, concentration of propionate in blood plasma was doubled, its contribution to milk galactose was increased to 1.5%, and proportions of milk odd-numbered fatty acids were increased. Propionate was incorporated largely into milk odd-numbered fatty acids (9:0, 11:0, 13:0, 15:0, 17:0). We conclude that small amounts of propionate can be incorporated into principal components of milk in the mammary gland of lactating goats.

Animals↗
PubMed1968

Biosynthesis of phytoquinones. Incorporation of L-[Me-14C,3H]methionine into terpenoid quinones and chromanols in maize shoots.

1. Radioactivity from l-[Me-(14)C,(3)H]methionine is incorporated into phylloquinone, plastoquinone, gamma-tocopherol, alpha-tocopherol, alpha-tocopherolquinone and ubiquinone in maize shoots. 2. Comparative studies with other terpenoids (squalene and beta-carotene) and chemical degradation of selected quinones (ubiquinone and plastoquinone) established that all the radioactivity is confined to nuclear methyl substituents. 3. In ubiquinone 76% of the radioactivity is in the methoxyl groups and 24% in the ring C-methyl group. 4. Taking the phytosterols as an internal reference and accepting the atomic ratio of (14)C/(3)H transferred from l-[Me-(14)C,(3)H]methionine to the supernumerary group at C(24) to be 1:2 the ratio of all the quinones and chromanols examined approached 1:3. After allowing for the fact that for plastoquinone, gamma-tocopherol, alpha-tocopherol and alpha-tocopherolquinone one nuclear methyl group is formed from the beta-carbon of tyrosine, these results show that one nuclear C-methyl group for phylloquinone, plastoquinone and gamma-tocopherol, two nuclear methyl groups for alpha-tocopherol and alpha-tocopherolquinone and one nuclear methyl and two methoxyl groups for ubiquinone are formed by the transfer of intact methyl groups from methionine. 5. From a comparison of the incorporation of (14)C radioactivity into these compounds it would appear that the methylation reactions involved in phylloquinone and plastoquinone biosynthesis take place in the chloroplast, whereas those involved with ubiquinone biosynthesis occur else-where within the cell.

Carbon Isotopes↗
PubMed1992

Mapping of histamine H1 receptors in the human brain using [11C]pyrilamine and positron emission tomography.

We have studied the characteristics of carbon-11 labeled pyrilamine as a radioligand for investigating histamine H1 receptors in human brain with positron emission tomography (PET). [11C]Pyrilamine is distributed evenly in proportion to cerebral blood flow at initial PET images. Later (after 45-60 min), 11C radioactivity was observed at high concentrations in the frontal and temporal cortex, hippocampus, and thalamus, and at low concentrations in the cerebellum and pons. The regional distribution of the carbon-11 labeled compound in the brain corresponded well with that of the histamine H1 receptors determined in vitro in autopsied materials. In six controls, the frontal and temporal cortices/cerebellum ratio increased during the first 60 min to reach a value of 1.22 +/- 0.071. Intravenous administration of d-chlorpheniramine (5 mg) completely abolished the specific binding in vivo in the frontal cortex and temporal cortex (cortex/cerebellum ratio, 0.955 +/- 0.015). The availability of this method for measuring histamine H1 receptors in vivo in humans will facilitate studies on neurological and psychiatric disorders in which histamine H1 receptors are thought to be abnormal.

Adult↗
PubMed1985

[Incineration system for the disposal of 125I-radioimmunoassay test tube wastes--confirmation of 125I decay in wastes].

Before incineration of disposed RIA test tubes, residual 125I radioactivity should be measured for the purpose of radiation safety. This confirmation method has been carried out according to the followings: Residual 125I radioactivity of test tubes in the plastic bag was measured from outside with the low-energy gamma-ray survey meter (S1371, Ohyo Kohken CO., Ltd.) newly developed by one of the authors. Gaseous 125I released from the residual 125I-compounds in test tubes by radiation self decomposition was adsorbed by the activated carbon fiber filter (ACFF), and was measured. From the above 2 methods, the minimum detectable concentration of residual 125I in waste tubes would be reached under a level of about 100 mBq/g (2.8 X 10(-6) muCi/g).

Iodine Radioisotopes↗
PubMed1975

Studies on the physiological significance of the lack of a pyruvate dehydrogenase complex in Hyphomicrobium sp.

Hyphomicrobium X was grown in media containing either methanol or ethanol as a carbon and energy source, with or without additional organic carbon sources. The organism transported pyruvate, malate and succinate into the cells, and incorporated their carbon skeletons into cellular material, but when each of these compounds was added as sole carbon and energy source none supported growth of the organism. Enzymic analysis of crude cell-free extracts failed to detect either a complete pyruvate dehydrogenase complex or an active E1 component. Furthermore, oxygen uptake experiments with whole cell suspensions did not show any oxidation of pyruvate, succinate or malate. The distribution of radioactivity amongst the amino acids in hydrolysates of cell protein obtained from organisms grown in the presence of [14C]pyruvate, [14C]acetate or [14C]succinate indicated that the organism is limited in its ability to metabolize pyruvate. Growth in the presence of [14C]pyruvate resulted in 93% of the total radioactivity recovered being associated with amino acids derived directly from pyruvate. In contrast, growth in the presence of [14C]acetate or [14C]succinate resulted in more-or-less uniform labelling of all biogenic classes of amino acids. These results are consistent with the lack of an active pyruvate dehydrogenase complex which would make it impossible for Hyphomicrobium X to convert pyruvate into acetyl-CoA and to generate energy from carbon compounds for which the energy metabolism relies on oxidation through tricarboxylic acid (TCA) cycle intermediates.

Acetates↗
PubMed1989

Is lipid peroxidation associated with DNA damage?

Specific binding to DNA of lipid peroxidation products was studied in rat hepatocytes labeled with [14C(U)]arachidonic acid after incubation at 37 degrees C either in the absence or in the presence of 200 microM FeSO4. The results obtained show that: (1) production of malondialdehyde-like thiobarbituric-reactive substances occurred in the absence of FeSO4 and was increased, albeit quite variably, by exposure to this pro-oxidant; (2) a low but appreciable binding of radioactivity to DNA and protein was constantly detected in 5 independent experiments; (3) there was no quantitative correlation between malondialdehyde formation and the amount of DNA-bound and protein-bound radioactivity, and any meaningful evidence of a GSH-depletion effect was absent. Taking into account the possible biosynthetic incorporation of radioactivity into DNA, the results of this study must be interpreted with caution, and solely as indicating that in the intact cell the covalent binding to DNA of reactive species generated by lipid peroxidation, if it occurs, should be minimal, corresponding in our experimental conditions approximately to 0.01 mumole of radioactive arachidonic acid per mole nucleotides.

Animals↗
PubMed1991

PET studies of potential chemotherapeutic agents--X. Synthesis of "no-carrier-added" (11C)-HECNU: the hydroxyethyl analog of the chemotherapeutic agent BCNU.

Carbon-11-labeled HECNU [1-(2-chloroethyl)-1-nitroso-3-(2-hydroxyethyl) urea] a potential chemotherapeutic agent, has been prepared by the nitrosation of the corresponding carbon-11-labeled urea, HECU, [1-(2-chloroethyl)-3-(2-hydroxyethyl) urea]. The isometric byproduct of nitrosation, 1-(2-chloroethyl)-3-nitroso-3-(2-hydroxyethyl) urea can be efficiently removed by preparative scale HPLC on a Partisil column. (11C)-HECU was prepared by reacting ethanolamine with (11C)-2-chloroethyl-isocyanate which was itself prepared by reacting [11C)-phosgene with 2-chloroethylamine hydrochloride suspended in dioxane at 60-65 degrees C. This synthesis yielded (11C)-HECNU with an average radiochemical purity of 98% in an average radiochemical yield of 18% relative to the radioactivity measured at the end of the 11C-phosgene introduction.

Carbon Radioisotopes↗
PubMed2001

Carbon-11 labelled cholecystokininB antagonists: radiosynthesis and evaluation in rats.

Three cholecystokinin type B (CCKB) receptor antagonists were labelled with 11C and evaluated ex vivo in rat biodistribution studies. The CCKB antagonists were YF 476 and two other compounds of the basic 3-ureido-1,4-benzodiazepine class. Following tail-vein administration of [11C]-YF 476 exceedingly low levels of radioactivity were found in all brain regions from 5 to 60 min post-injection. Similar results were obtained using the other two 11C-labelled CCKB antagonists. In light of the very poor brain penetration of these compounds, reports on the central nervous system activity of this class of CCKB antagonists should be viewed with caution.

Animals↗
PubMed2005

Mechanism of uranium removal from the aqueous solution by elemental iron.

The effectiveness of elemental iron (Fe(0)) to remove uranium (U) from the aqueous phase has been demonstrated. While the mitigation effect is sure, discrepancies in the removal mechanism have been reported. The objective of this study was to investigate the mechanism of U(VI) removal from aqueous phases by Fe(0). For this purpose, a systematic sequence of bulk experiments was conducted to characterize the effects of the availability and the abundance of corrosion products on U(VI) removal. Results indicated that U(VI) removal reactions did not primary occur at the surface of the metallic iron. It is determined that U(VI) co-precipitation with aging corrosion products is a plausible explanation for the irreversible fixation under experimental conditions. Results of XRD analyses did no show any U phases, whereas SEM-EDX analyses showed that U tended to associate with rusted areas on the surface of Fe(0). Recovering U with different leaching solutions varied upon the dissolution capacity of the individual solutions for corrosion products, showing that the irreversibility of the removal depends on the stability of the corrosion products. U(VI) co-precipitation as removal mechanism enables a better discussion of reported discrepancies.

Adsorption↗