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At least 307 records · Page 17Linked to original sources
PubMed1990

Chemical processing for production of no-carrier-added selenium-73 from germanium and arsenic targets and synthesis of L-2-amino-4-([73Se]methylseleno) butyric acid (L-[73Se]selenomethionine).

The Ge(4He, xn) and 75As(p, 3n) reactions were compared as the best potential routes for routine production of selenium-73 (73Se) for medical applications. With 26 MeV alpha particles, available with compact cyclotrons, the first reaction required an enriched 70Ge target of sodium metagermanate to give a production yield of 1 mCi/microAh (0.037 GBq/microAh) in a 105 mg/cm2 target. With 55 MeV protons the As(p, 3n) reaction on natural arsenic yielded 20 mCi/microAh (0.74 GBq/microAh) in a 685 mg/cm2 target. A simple method was developed and optimized for both targets in order to isolate and purify the no-carrier-added selenium in the elemental form with a radiochemical yield greater than 75% in less than 90 min. An automated radiochemical processing unit has been designed for the routine production of 100-150 mCi (3.7-5.5 GBq) batches of carrier-free 73Se ready for radiopharmaceutical labeling. 30 mCi (1.11 GBq) (EOS) of L-2-amino-4-([73Se]methylseleno) butyric acid (L-[73Se]selenomethionine) ready for injection with a specific activity of 5 Ci/mmol (185 GBq/mmol) (EOS) were obtained through a fast chemical synthesis. Radiation absorbed dose estimates for L-[73Se]selenomethionine have been determined. A value of 0.70 rem/mCi (0.19 mSv/MBq) administered was calculated for the risk from irradiation in man. The first human PET investigation with [73Se]selenomethionine showed a very good delineation between liver and pancreas.

Arsenic↗
PubMed1991

Reusable gels for germanium-68 sources.

Two water-soluble gels, gelatin and Carbowax, were mixed with radioactive 68Ge solutions and evaluated for their use as long-lived (half-life, 280 days) radioactive sources. These gels melt at 40-50 degrees C and solidify at room temperature. The amount of 68Ge mixed with them can be increased or decreased as needed, eliminating waste of 68Ge. These gel sources also may replace short-lived 68Ga (half-life 68 min) as attenuation correction sources in positron emission tomography (PET) and reduce frequency of source preparation, thus reducing exposure of PET operators to radiation.

Gelatin↗
PubMed2006

Application of PENELOPE code to the efficiency calibration of coaxial germanium detectors.

The code PENELOPE is applied here to the efficiency calibration exercise described in the EUROMET project 428 [Lépy et al., 2001. Appl. Radiat. Isot. 55, 493]. We evaluated the peak efficiencies for a coaxial HPGe detector in the range 60-2000 keV, for point sources located at various distances from the detector and for a cylindrical box containing two different matrixes: a low-density silica and a hydrochloric acid solution. After an optimization of several detector parameters, the results were in good agreement with the experimental values.

Algorithms↗
PubMed2006

Production and separation of no-carrier-added radioactive tracers of yttrium, strontium and rubidium from heavy-ion irradiated germanium target: applicability to the standardization of a separation technique for production of positron-emitting radionuclide 86Y.

Among various positron-emitting radionuclides, certain radioisotopes of Y, Sr and Rb have important applications in diagnostic and therapeutic nuclear medicine. In the present work, an attempt has been made to produce some of those radioisotopes by irradiating a natural Ge-target material with heavy-ion oxygen ((16)O(+6)) projectiles. An effective radiochemical separation scheme was developed to isolate Y, Sr and Rb radiotracers from the irradiated Ge-matrix in no-carrier-added form with a view to applying those radiotracers for standardization of a technique for the radiochemical separation of Y from natural Sr target. The standardized separation technique could be utilized for the production of the positron-emitting (86)Y from an enriched (86)Sr target irradiated at a medical cyclotron.

Electrons↗
PubMed1975

Similarity in uptake and retention of trace amounts of 31 silicon and 68 germanium in rat tissues and cell organelles.

Uptake of Si and Ge (chemical analogue of Si) in rat tissues was compared to establish their subcellular localization and determine if Ge could be used to trace Si in situ. 31Si and 68Ge were found in tissues and in cell organelles after injection of 31Si (OH) 4 or 68Ge (OH) 4. Accumulation of 31Si and 68Ge in the tissues increased for 30 minutes, declined rapidly about 30 minutes and then was gradually but steadily depleted. Simultaneous double labelling with 31Si and 68Ge produced concomitant accumulation and release of both isotopes. After a single IP injection, some 68Ge remained in the spleen and kidney for up to 20 days. The 31Si and 68Ge concentration in the tissues and cell organelles increased linearly with the amount administered (31Si, 10-4 to 10-2 g/kg body wt and 68Ge, 10-9 to 10-3 g/kg body wt). Thus, substitution of 68Ge for 31Si can extend the limit of detection of Si by at least 5 orders of magnitude. Both 31Si and 68Ge were water extractable (47%-74% and 38%-89%, respectively) from liver cell organelles; 45%-81% 31Si and 66%-90% 68Ge were extractable in 10% TCA, while only 10%-59% of either isotope were extractable in organic solvents (acetone, chloroform, ethanol). A small percentage of Si may be bound or polymerized.

Animals↗
PubMed2002

Germanium-68 as a tracer for silicon fluxes in freshwater sediment.

The sorption of Si may decisively influence the P dynamics in surface sediment through competitive ligand exchange mechanisms. Many aspects of the process, such as the impact of Si dissolving from diatoms, are both insufficiently known and difficult to monitor by quantitative analyses due to the ubiquitousness of Si in sediment. Since the radioactive isotopes of Si have impractical half-times, the applicability of 68Ge as a tracer for Si additions in both inorganic and biogenic form to freshwater sediment (Lake Vesijärvi, Southern Finland) was studied in a 24-h laboratory experiment. The 68Ge-label was added to the sediment with either inorganic Si (940mg l(-1)) or diatoms (3.2 x 10(6) cellsl(-1)), and the distributions of the 68Ge-label and the different forms of added Si between the interstitial water and sequentially extracted, solid-phase sediment pools were critically examined. The inorganic Si addition significantly increased the amount of Si in the interstitial water and in the reversibly bound fraction, while the diatom addition had no discernible effects. The relative distribution of Si and 68Ge between the various sediment pools indicated that the first sorption phase of the added inorganic Si was similar to that reported for P. The high concentration of diatom-derived 68Ge-labelled Si in the interstitial water and in the easily soluble, reversibly bound pool indicated rapid dissolution of the added diatoms. The comparable distributions of the diatom-derived and inorganic Si-derived 68Ge-label within the studied pools indicated that the sorption of Si dissolving from diatoms in surface sediment closely resembles that of an inorganic addition of Si. Caution about the chemical speciation of the 68Ge-label is, however, advisable in sediment environments. Fractionation procedures designed for e.g. P may also be of limited use when applied to a different element, such as Si.

Adsorption↗
PubMed2002

Distribution of natural and anthropogenic radionuclides in soil and beach sand samples of Kalpakkam (India) using hyper pure germanium (HPGe) gamma ray spectrometry.

Pre-operational survey at Kalpakkam coast, indicated elevated gamma background radiation levels in the range of 100-4000 nGy h(-1) over the large tracts of the coastal sands due to the presence of pockets of monazite mineral in beach sands. In view of the prevalence of monazite, a systematic gamma spectrometric study of distribution of natural radionuclides in soil and beach sand samples collected from the terrestrial and coastal environment of Kalpakkam was performed and concentrations of primordial radionuclides such as 238U, 232Th and 40K and anthropogenic radionuclide 137Cs were determined. The concentrations of 238U, 232Th and 40K in soil samples were 5-71, 15-776 and 200-854 Bq kg(-1) dry, respectively. In beach sand samples, 238U, 232Th and 40K contents varied in the range of 36-258, 352-3872 and 324-405 Bq kg(-1) dry, respectively. The total absorbed gamma dose rate in air due to the presence of 238U, 232Th and 40K in Kalpakkam soil samples varied between 24 and 556 nGy h(-1) with a mean of 103 nGy h(-1). The contribution to the total absorbed gamma dose rate in air in the decreasing order was due to the presence of 232Th (76.4%), followed by 40K (16.9%) and 238U (6.7%) in Kalpakkam soils. However, in beach areas of Kalpakkam, the presence of 232Th in beach sand contributed maximum (94.0%) to the total absorbed gamma dose rate in air followed by 238U (4.7%) and minimum contribution was by 40K (1.3%). 137Cs in Kalpakkam soils ranged from < or = 1.0 to 2.8 Bq kg(-1) dry, which was 1-3 order of magnitude less than the concentration of primordial radionuclides in soil.

Cesium Radioisotopes↗
PubMed2006

Gold-catalyzed 1,2-migration of silicon, tin, and germanium en route to C-2 substituted fused pyrrole-containing heterocycles.

An efficient method for the synthesis of fused pyrroloheterocycles from diverse propargyl-substituted heterocycles in the presence of Au-catalyst has been developed. The cascade transformation proceeds via alkyne-vinylidene isomerization with concomitant 1,2-shift of hydrogen, silyl, and stannyl groups. Remarkably, it was also shown that previously unknown 1,2-migration of a germyl group upon alkyne-vinylidene rearrangement occurs under these reaction conditions. This method allows for mild and efficient synthesis of diverse C-2 substituted N-containing heterocycles.

Alkynes↗
PubMed2006

Germanium nanowire epitaxy: shape and orientation control.

Epitaxial growth of nanowires along the 111 directions was obtained on Ge(111), Ge(110), Ge(001), and heteroepitaxial Ge on Si(001) substrates at temperatures of 350 degrees C or less by gold-nanoparticle-catalyzed chemical vapor deposition. On Ge(111), the growth was mostly vertical. In addition to 111 growth, 110 growth was observed on Ge(001) and Ge(110) substrates. Tapering was avoided by the use of the two-temperature growth procedure, reported earlier by Greytak et al.

Germanium↗