The preparation of the 99mTcN-complexes of gluconate, EHDP, HIDA and PIPIDA by substitution reactions of 99mTcNCl4− is described. Studies of the distribution of these complexes in mice indicate that the presence of the Tc-nitrido group significantly alters the biological properties of the 99mTc-complexes formed using these ligands. Results suggest that the 99mTcN-complexes of these ligands are labile and undergo some ligand exchange in vivo.
In this paper we report the successful labelling of cryptolepine with 131I using the chloramine T method. Quality control by ITLC of the labelled product showed 80% labelling but when the mixture was equilibrated with some amberlite (Cl−) anion resin to exchange the excess free iodide, the radiochemical purity was raised to >90%. Preliminary biodistribution in a rat did not show specific localisation of the tracer; rather, rapid clearance from the blood was indicated. It appears that its main excretory pathway is the hepatobiliary tract despite its relatively small molecular weight of 365. Also, despite i.v. administration, an appreciable 8% uptake was found in the stomach at 1 h post injection, indicating the process of enterohepatic reflux. These findings may have some bearings on the antimicrobial property of the plant.
CaF2 thermoluminescence dosimeters (TDL) were used to measure the apparent absorbed dose due to 16N-decay radiation, such as is found in nuclear reactor coolant or in air due to the 16O(n,p)16N activation by fast neurons. By comparison with an ionization chamber calibrated with a 60Co source, it was found that the TLD underestimated the dose for about 7-MeV γ-rays by a factor 1.8, while the ionization chamber reading was low by a factor 2.6 when compared with the calculated dose.
The production and use of radioactive standard sources suitable for the efficiency calibration of Si(Li) and germanium detectors in the energy range from 5 to 40 keV is described. Special attention was given to self absorption which could be reduced to about 1% or less by applying appropriate source preparation procedures.
A number of metal selenides were investigated as target material for the production of 75Br by the 76Se(p,2n)75Br reaction. Ag2Se, CuAgSe, and Cu2Se met the rqquirements for an economical and fast production procedure. These selenides were found to be stable during bombardment with 1–4 μA 28 MeV protons (beam dimension 0.4 cm2) and at the dry distillation temperature of 1473 K. A target system was developed for radiobromine production with a 7 μA 28−22 MeV proton beam on Cu2Se. At EOB the calculated thick target yield is 1.59 GBq/μAh (43 mCi/μAh) and the radionuclidic purity is 98.6%. The radiobromine was separated from Cu2Se by dry distillation at 1473 K and collected for 80–95% on platinum wool pretreated with CaCl2. Radiochemical analysis showed the radiobromine to be Br− for 95% and BrO3− for 5%. The total loss of selenide after irradiation and distillation was found to be less than 0.1%.
An instrument and a method for investigation of root bioactivity in plants injected with 75Se are presented. The design of the detection probe is described and its response in soil is surveyed. The scanning of radioactivity in the root system is performed automatically by means of a digital depth control, the function of which is also described. The method has been used for several years at this department and the results of a laboratory test are presented.
The δ13C values of 20 breath samples and 10 tank-CO2 samples (δ13C values ranged from −31.3 to +148.9% vs PDB) and the CO2 concentrations of three breath samples and 10 tank-CO2 samples were measured with a commercial prototype of a diode-laser i.r. spectrophotometer, MAT I. The results were compared with those obtained by gas-isotope-ratio mass spectrometry and by gas chromatography. Precisions (sx, n = 10) of 0.2% and 0.6% were calculated for 13C/12C ratios and CO2 concentrations, respectively, using the MAT I system.