Experiences in routine production of123I in Manitoba for delivery to other Canadian centres

An experience at¹²³I production with a low beam current cyclotron used in combination with the¹²⁴Te(p, 2n)¹²³I reaction on 90.8% enrichment¹²⁴Te is described.     

Cross-section calculations of proton induced (p,n) and (p,2n) reactions for production of diagnostic 67Ga, 81Rb, 111In, 123,124I, 123Cs and 123Xe radioisotopes

Investigation of pre-equilibrium (PEQ) and equilibrium (EQ) effects on proton induced reactions for production of radioisotopes are very important. Therefore, in this study, we have calculated the PEQ and EQ cross-sections for ⁶⁷Zn(p,n)⁶⁷Ga, ⁶⁸Zn(p,2n)⁶⁷Ga, ⁸²Kr(p,2n)⁸¹Rb, ¹¹¹Cd(p,n)¹¹¹In, ¹¹²Cd(p,2n)¹¹¹In, ¹²³Te(p,n)¹²³I, ¹²⁴Te(p,2n)¹²³I, ¹²⁴Te(p,n)¹²⁴I and ¹²⁴Xe(p,2n)¹²³Cs reactions for production diagnostic radioisotopes. Calculations have been performed by using the hybrid model, geometry dependent hybrid model and full exciton model of PEQ reaction mechanism with 1–40 MeV proton incident energy. We have also investigated the EQ effects on these reactions using the Weisskopf–Ewing model in the same energy range. The excitation functions including the PEQ and EQ effects on these reactions are evaluated by using the ALICE/ASH (2006) and the TALYS 1.4 (2011) codes. Our results have shown that using these codes is suitable for production diagnostic isotopes mentioned above. To obtain excitation functions for producing the diagnostic radioisotopes the PEQ mechanism has been found more dominant than that of the EQ. The results are discussed and compared with the available experimental data.     

Experiences in the routine production of123I via the124Te(p, 2n)123I reaction with a low energy cyclotron

This paper deals with the results and experimental observations obtained in routine production of¹²³I via¹²⁴Te(p, 2n)¹²³I reaction, using the low energy cyclotron (protons, E_max=22 MeV) at the German Cancer Research Center in Heidelberg. The reaction was studied during the past 4 years using¹²⁴TeO₂ targets with various levels of enrichment. The purpose of the study was to determine which target material provided the highest quality and most economical production of¹²³I. A viable routine production was defined as one in which¹²³I could be conveniently and reproducably prepared in reasonable purity while maintaining a low cost for the entire process. Different methods of sublimation of¹²³I activity from the¹²⁴TeO₂ target were examined to determine the optimal conditions for recovery of radioactivity and recycling of target material. A rapid method is described which permits quantitative separation of¹²³I while allowing only a negligible loss of¹²⁴TeO₂.     

Development of an ion-exchange method for separation of radioiodine from tellurium and antimony and its application to the production of 124I via the 121Sb(α,n)-process

A novel anion-exchange chromatographic method for separation of radioiodine from an antimony target irradiated with ³He- or α-particles was developed, with separation yield of radioiodine amounting to 90 ± 5 % and its decontamination factor from the Te and Sb radionuclides to ~10⁴. The optimized separation method developed was then applied to the production of ¹²⁴I via the ¹²¹Sb(α,n)¹²⁴I process using a highly enriched ¹²¹Sb target. Quality control tests showed that the separated ¹²⁴I occurred >99 % as iodide and the longer lived impurities ¹²⁶I and ¹²⁵I amounted to 0.16 % and <0.05 %, respectively. The trace level of inactive Sb impurity was determined by ICP–OES.     

Production of123I using the CV-28 cyclotron at IPEN-CNEN/SP

These studies had the purpose of establishing the optimal conditions for the production of¹²³I through the¹²⁴Te (p, 2n)¹²³I reaction, using the CV-28 Cyclotron (E_max=24 MeV for protons) at IPEN-CNEN/SP. Two different targets (TeO₂ and TeO₂+2% Al₂O₃) were irradiated in order to check their physical resistance against beam current (up to 12 A) and length of irradiation (10 min — 2h), and to evaluate the recovery of the radioiodine produced, by a dry distillation process with a high frequency induction furnace. Later on, enriched¹²⁴TeO₂ (96.2%) targets were irradiated, and¹²³I was produced routinely with a production yield of (3. 31±0.07) mCi/Ah, 1.7% of¹²⁴I at EOB and radiochemically pure.     

Iodine-123 production at a small cyclotron for medical use

An improved method has been developed to obtain highly enriched [¹²³Te] tellurium for the production of medically important¹²³I. Excitation function of the¹²³Te(p,n)¹²³I reaction, production yields and radionuclidic impurity levels were determined as a function of bombarding energy and target thickness.     

Pure iodine-123 production by small cyclotron for medical use

For improvement of radionuclidic purity of¹²³I a method was elaborated to obtain highly enriched [¹²³Te] tellurium. Using this new TeO₂ target the optimum irradiation conditions have been investigated for the production of¹²³I via¹²³Te (p,n)¹²³I and the radionuclide impurity levels were also determined.     

Separation of trace elements,In(III), Sn(IV), Sb(V) and Te(IV) by adsorption on activated carbon and graphite

Adsorption behaviour of trace elements, In(III), Sn(IV), Sb(V) and Te(IV) on activated carbon and graphite powder was studied. Adsorption characteristics of the ions enabled the separation of In(III)–Sn(IV), Sn(IV)–Sb(V) and Sb(V)–Te(IV) pairs. Applications to practical separation, milking of^113mIn from¹¹³Sn, removal of tin impurity from¹¹⁹Sb, and milking of¹¹⁹Sb from^119mTe, are presented.     

123I production at the Milan AVF cyclotron

The production of¹²³I from enriched¹²⁴Te is described. Preliminary experiments on a distillation separation of iodine from the Te target have been performed and the method seems promising in comparison to the time-consuming chemical separation technique.     

Excitation functions of proton induced nuclear reactions on natural tellurium up to 18 MeV for validation of isotopic cross sections

Summary Excitation functions of proton induced nuclear reactions on natural Te were investigated up to 18 MeV. Cross sections for production of ^{121,123,124,126,128,130g}I and ^121gTe were measured. The new experimental data were compared with the results of ALICE-IPPE model calculations and with data found in the literature and measured on natural or enriched Te targets. The new data can be effectively used for validation of recommended cross sections of medically relevant ¹²³I and ¹²⁴I.     

Preparation of a118Te/118Sb radionuclide generator

The development of a new radionuclide generator, based on¹¹⁸Te/¹¹⁸Sb, has been studied. The 3.5 minute¹¹⁸Sb daughter activity decays principally by positron emission and has potential use as a flow tracer. The¹¹⁸Te parent is conveniently produced by proton bombardment of antimony targets. A simple and efficient scheme for the separation of radiotellurium from proton-irradiated antimony targets has been developed, and thin-target cross sections for¹²¹Sb(p, 4n)¹¹⁸Te and competing reactions have been determined. For antimony targets irradiated with 46 MeV protons, the yields (mCi/g Ah) of¹¹⁸Te,^119mTe and¹¹⁹Te were measured to be 0.71, 0.33 and 1.9, respectively. The adsorption and elution characteristics of activated carbon for tellurium have been evaluated for use as a column chromatography adsorbent in a¹¹⁸Te/¹¹⁸Sb generator. The conditions for optimal¹¹⁸Sb elution and minimal¹¹⁸Te breakthrough for promising systems are presented.     

123Sb NQR and 19F NMR study of potassium,rubidium, and cesium heptafluorodiantimonates(iii)

The dynamics of crystal lattices of potassium, rubidium, and cesium heptafluorodiantimonates(iii) and specific features of internal rotations of the Sb₂F₇ fluoride groups in these compounds were studied using ¹²³Sb NQR in the temperature interval from 77 to 325 K and ¹⁹F NMR in the temperature interval from 240 to 470 K in combination with X-ray diffraction and thermogravimetric analyses. The distinctions in the dynamic behavior of the fluoride ions with changing the size (polarizability) of outer-sphere cations are discussed. The structural phase transition in CsSb₂F₇ was revealed at 425—430 K accompanied by the appearance of a high ion conductivity ( 1.3·10^–3 S cm^–1 at 450 K). A second type phase change can exist at 220—270 K.     

Facile Synthesis of 5-Aryl-N-(pyrazin-2-yl)thiophene-2-carboxamides via Suzuki Cross-Coupling Reactions,Their Electronic and Nonlinear Optical Properties through DFT Calculations

Synthesis of 5-aryl-N-(pyrazin-2-yl)thiophene-2-carboxamides (4a–4n) by a Suzuki cross-coupling reaction of 5-bromo-N-(pyrazin-2-yl)thiophene-2-carboxamide (3) with various aryl/heteroaryl boronic acids/pinacol esters was observed in this article. The intermediate compound 3 was prepared by condensation of pyrazin-2-amine (1) with 5-bromothiophene-2-carboxylic acid (2) mediated by TiCl₄. The target pyrazine analogs (4a–4n) were confirmed by NMR and mass spectrometry. In DFT calculation of target molecules, several reactivity parameters like FMOs (E_HOMO, E_LUMO), HOMO–LUMO energy gap, electron affinity (A), ionization energy (I), electrophilicity index (ω), chemical softness (σ) and chemical hardness (η) were considered and discussed. Effect of various substituents was observed on values of the HOMO–LUMO energy gap and hyperpolarizability. The p-electronic delocalization extended over pyrazine, benzene and thiophene was examined in studying the NLO behavior. The chemical shifts of ¹H NMR of all the synthesized compounds 4a–4n were calculated and compared with the experimental values.     

Production of123I on linear electron accelerator using highly-enriched124Xe

Highly enriched xenon¹²⁴Xe /99.85%/ has been used for the experimental production of iodine¹²³I by the /,n/ reaction. As the radiation source served a 30–45 MeV electron beam produced by a linear accelerator and converted by a tungsten converter to -radiation. The yield and radionuclidic purity of¹²³I have been estimated, the content of isotopic impurities /¹²⁴I and¹²⁵I/ being for 30 MeV irradiations lower than 4×10^–3%/.     

Variations of the shape of123Sb NQR tines in phase transitions in K2SbF5

Variations of the shape of¹²³Sb NQR lines in phase transitions in a new ionic conductor, potassium pentafluoroantimonite(ui), in the temperature range from 77 to 430 K were studied. The transition from a paraelectric phase to a commensurate phase occurs via incommensurate and commensurate-modulated phases.Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 10, pp. 2497–2500, October, 1996.     

Enriched stable isotopes for 123I production: Pathways and prospects

Large-scale production of radioisotopes for medical application was impeded by limited capabilities of the electromagnetic separation. Nowadays the centrifuge separation process involves more than two dozens of chemical elements. The cost of isotopes is incomparably lower than of those produced by electromagnetic separation, which has made enriched isotopes more practicable and has extended their application scope. The development of new isotope targets has ensured the realization of more effective schemes of ¹²³I production. The processes of ¹²⁴Xe and ¹²³Te production are reviewed.     

Kinetics and Mechanism of the Nucleophilic Substitution of Tellurium(II) Dialkanethiolates,Te(SR1)2 with Thiols,HSR2

The equilibrium reaction between tellurium(II) dithiolates and thiols, Te(SR¹)₂ + 2 HSR² ? Te(SR²)₂ + 2 HSR¹ was studied by means of ¹H- and ¹²⁵Te NMR spectroscopy and ab initio quantum chemical methods. It was found that the reaction is catalyzed by Brønsted acids and bases, the catalytic activity corresponding to the strength of the respective acid or base. Investigation of the initial step of the reaction, Te(SR¹)₂ + HSR² ? Te(SR¹)(SR²) + HSR¹, showed it to proceed according to first order kinetics for Te(SR¹)₂, HSR² and for the catalyst. Ab initio geometry optimizations and frequency calculations suggest [Te(SR¹)(HSR¹)(HSR²)]⁺ and [Te(SR¹)₂(SR²)]^? to be stable intermediates and not transition states in the acid and base catalyzed reactions, respectively. The reaction hence proceeds via an additional elimination rather than an S _N 2 mechanism. The catalytic activity displayed by acids and bases can be applied to reduce the temperature in synthesis of thermally labile tellurium(II) dithiolates.     

Performance of gamma camera collimators used for single photon emission computed tomography imaging with 123I-isopropyl iodoamphetamine

123I Produced by 124Te(p, 2n)123I reaction is contaminated with 124I (less than 5%) and 126I (less than 0.3%). High energy photons from these mixed radioiodine compromise seriously image quality due to scattered photons and to septal penetration in the collimator. Four collimators of LEAP (for low energy all purpose), LEHR (for low energy high resolution), MESI (for medium energy made by Siemens) and MENU (for medium energy made by nuclear technology) mounted on a rotating gamma camera (Siemens, ZLC-7500), were examined in order to select a suitable collimator for 123I SPECT (single photon emission computed tomography) imaging. Sensitivities were measured with a plane source (5 X 5 X 0.5 cm) at the collimator face and distances from 2 to 30 cm in air. And, spatial resolutions in FWHM (full width at half maximum) and FWTM (full width at tenth maximum) were determined from line spread functions with planar and SPECT imaging. From the comparison of collimator performances with 99mTc and 123I, both collimators for low energy were not useful for 123I imaging. In other two collimators for medium energy, however, apparently the effect of septal penetration by the higher energy photons were also recognized, MENU with high geometrical resolution was more suitable for 123I SPECT imaging compared with MESI. And, it is important to perform the SPECT imaging with radius as short as possible.     

Rapid separation of carrier-free inorganic and organic compounds of radioiodine and astatine by high-pressure liquid chromatography

The radioisotopes¹²³I (T=13.3 h) and, potentially,²¹¹At(T=7.2 h) find increasing interest for radiopharmaceutical applications in diagnosis and therapy. They were produced via the¹²²Te(α, 3n)¹³Xe(α⁺)¹³I and the²⁰⁹Bi(α, 2n)²¹¹At processes. Fast and efficient separations of carrier-free species obtained from target processing, as well as from classical or decay-induced synthesis were archieved by means of high-pressure ion-exchange and partition chromatography. Inorganic forms (X⁻, XO ₃ ⁻ , At⁺) could be identified and separated on pretreated Aminex A 27 and A 7 resins, and biomolecules such as 5-halodeoxyuridines and-uracils on Aminex A 25 resins and Merckosorb Si 60 silica. The chromatographic methods can also be used for stability tests of radiopharmaceuticals in biochemical mixtures, notably physiological fluids.     

New cross section data on68Zn(p, 2n)67Ga andnatZn(p,xn)67Ga nuclear reactions for the development of a reference data base

Excitation functions were measured by stacked-foil technique for the⁶⁸Zn(p, 2n)⁶⁷Ga,⁶⁸Zn(p,3n)⁶⁶Ga,^natCu(p,xn)⁶²Zn,^natZn(p,xn)⁶⁷Ga,^natZn(p,xn)⁶⁶Ga,^natZn(p,px)⁶²Zn and^natZn(p,αx)⁶¹Cu nuclear reactions in the energy range from 15–35 MeV. The experimental excitation functions were compared with published data. Our present measurements not only increase the number of available cross section data points for the above reactions, but for some reactions (and in some energy regions) values are presented for the first time.