Optimization of conditions for ⁶⁷Cu photonuclear production

Radiopharmaceuticals based on the ⁶⁷Cu isotope have found wide use in immunotherapy. The present paper analyzes the conditions of ⁶⁷Cu production by the ⁶⁸Zn(γ,p) ⁶⁷Cu reaction at an electron accelerator in relation to the target isotope and hot impurities yield, as well as the radiation risks. Cons...

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Datum:2015
Hauptverfasser: Dovbnya, A.N., Dolzhek, M.A., Pugachev, G.D., Repikhov, O.A., Torgovkin, A.V., Uvarov, V.L., Shestakova, V.S., Shramenko, B.I.
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Veröffentlicht: Національний науковий центр «Харківський фізико-технічний інститут» НАН України 2015
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Zitieren:Optimization of conditions for ⁶⁷Cu photonuclear production / A.N. Dovbnya, M.A. Dolzhek, G.D. Pugachev, O.A. Repikhov, A.V. Torgovkin, V.L. Uvarov, V.S. Shestakova, B.I. Shramenko // Вопросы атомной науки и техники. — 2015. — № 6. — С. 160-164. — Бібліогр.: 7 назв. — англ.

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author Dovbnya, A.N.
Dolzhek, M.A.
Pugachev, G.D.
Repikhov, O.A.
Torgovkin, A.V.
Uvarov, V.L.
Shestakova, V.S.
Shramenko, B.I.
author_facet Dovbnya, A.N.
Dolzhek, M.A.
Pugachev, G.D.
Repikhov, O.A.
Torgovkin, A.V.
Uvarov, V.L.
Shestakova, V.S.
Shramenko, B.I.
citation_txt Optimization of conditions for ⁶⁷Cu photonuclear production / A.N. Dovbnya, M.A. Dolzhek, G.D. Pugachev, O.A. Repikhov, A.V. Torgovkin, V.L. Uvarov, V.S. Shestakova, B.I. Shramenko // Вопросы атомной науки и техники. — 2015. — № 6. — С. 160-164. — Бібліогр.: 7 назв. — англ.
collection DSpace DC
container_title Вопросы атомной науки и техники
description Radiopharmaceuticals based on the ⁶⁷Cu isotope have found wide use in immunotherapy. The present paper analyzes the conditions of ⁶⁷Cu production by the ⁶⁸Zn(γ,p) ⁶⁷Cu reaction at an electron accelerator in relation to the target isotope and hot impurities yield, as well as the radiation risks. Consideration has been given to some variants of the technological target 40 g in weight made from natural zinc, and one enriched up to 99% in the ⁶⁸Zn isotope. The target exposition to bremsstrahlung with end-point energy 30 and 60 MeV was studied. It has been found that the use of enriched target results in reduction of both the radiation risk (down to 10⁻⁴) and the scope of waste han-dling procedures. Радіофармпрепарати на основі ізотопу ⁶⁷Cu широко використовуються в імунотерапії. У повідомленні проаналізовані умови його виробництва на прискорювачі електронів за реакцією ⁶⁸Zn(γ,n)⁶⁷Cu відносно виходу цільового продукту, а також гарячих домішок і радіаційних ризиків. Розглянуто варіанти технологічної мішені масою 40 г із цинку природного складу і збагаченого до 99% за ізотопом ⁶⁸Zn, активованою гальмівним випромінюванням із граничною енергією 30 і 60 МеВ. Показано, що при використанні збагаченої мішені радіаційний ризик знижується до 10⁻⁴, а також значно зменшується обсяг процедур з відходами. Радиофармпрепараты на основе изотопа ⁶⁷Cu широко используются в иммунотерапии. В сообщении проанализированы условия его производства на ускорителе электронов по реакции ⁶⁸Zn(γ,n)⁶⁷Cu в отношении выхода целевого продукта, а также горячих примесей и радиационных рисков. Рассмотрены варианты технологической мишени массой 40 г из цинка природного состава и обогащенного до 99% по изотопу ⁶⁸Zn, активированной тормозным излучением с граничной энергией 30 и 60 МэВ. Показано, что при использовании обогащенной мишени радиационный риск снижается до 10⁻⁴, а также значительно уменьшается объем процедур с отходами.
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fulltext ISSN 1562-6016. ВАНТ. 2015. №6(100) 160 OPTIMIZATION OF CONDITIONS FOR 67Cu PHOTONUCLEAR PRODUCTION A.N. Dovbnya, M.A. Dolzhek, G.D. Pugachev, O.A. Repikhov, A.V. Torgovkin, V.L. Uvarov, V.S. Shestakova, B.I. Shramenko National Science Center “Kharkov Institute of Physics and Technology”, Kharkov, Ukraine E-mail: uvarov@kipt.kharkov.ua Radiopharmaceuticals based on the 67Cu isotope have found wide use in immunotherapy. The present paper ana- lyzes the conditions of 67Cu production by the 68Zn(γ,p) 67Cu reaction at an electron accelerator in relation to the target isotope and hot impurities yield, as well as the radiation risks. Consideration has been given to some variants of the technological target 40 g in weight made from natural zinc, and one enriched up to 99% in the 68Zn isotope. The target exposition to bremsstrahlung with end-point energy 30 and 60 MeV was studied. It has been found that the use of enriched target results in reduction of both the radiation risk (down to 10-4) and the scope of waste han- dling procedures. PACS: 07.85.-m, 81.40wx, 87.53-j, 87.53Wz INTRODUCTION Nowadays, commercial isotope production is mainly based on the use of nuclear reactors (see, e.g., ref. [1]). However, the fission of 235U results in the production of side radioactive products, thereby giving rise to the problem of long-lived radioactive waste. Besides, the use of highly enriched 235U is connected with the danger of its uncontrolled proliferation. An alternative method of radioisotope production lies in the use of heavy-particle/electron accelerators. Thus, 67Cu, as one of the most promising isotopes for radiotherapy of tumors by monoclonal antibodies, can be produced in the reactions under the action of neu- trons, protons, α-particles, and also, high-energy pho- tons. It has been demonstrated in ref. [2] that the photo- nuclear technology using the reaction 68Zn(γ,р)67Cu provides the best conditions for the desired isotope pro- duction with regard to its total yield and the radionu- clide-impurity production, even if a target made from natural zinc is used. The major sources of isotope production hazards originate from radiation of the target isotope, hot impu- rities, and also target device elements. The individual risk r of stochastic effects occurrence due to personnel irradiation is given by the relation r=rεD, where D is the individual absorbed dose, and rε is the total death risk factor due to radiation, taken to be 5.6·10-2 events per 1 man·Sv for professional irradiation. By interna- tional practice, the boundary value of the individual risk of personnel irradiation is taken to be 10-3 per annum [3]. The present paper is concerned with the sources and levels of radiation risks, and also, with the ways of their reduction under 67Cu producing at an electron accelera- tor. 1. MAIN REACTIONS At activation of a zinc target of natural isotopic composition (64Zn – 48.6%, 66Zn – 27.9%, 67Zn – 4.1%, 68Zn – 18.8%, 70Zn – 0.6%) in the mixed X,n-radiation field, the yield of 67Cu and hot impurities, which give the main dose-forming contribution to the target radia- tion, goes by the reactions: 68Zn (γ,р) 67Cu, 67Zn (n,р) 67Cu, 64Zn (γ,2n) 62Zn, 64Zn (γ,n) 63Zn, 70Zn (γ,n) 69mZn, 68Zn (n,γ) 69mZn, 64Zn (n,р) 64Cu, 66Zn (γ,nр) 64Cu, 66Zn (γ,n) 65Zn, 64Zn (n,γ) 65Zn. In the subsequent calculations, the maximum 67Cu activity of the natural zinc target by EOB was put to be 3.7·109 Bq (100 mCi). The concomitant radionuclide activity data required for estimating the radiation risks were obtained from the experiments at an 36 MeV elec- tron accelerator when irradiating the 40g natural zinc target in the (240 μA; 10 h) run. The data on the 63Zn yield were obtained by calculations using the following formula max 0 max( ) ( , ) th E E N N E f E E dE γ γ γ γσ= ∫ , (1) where N0_is the number of nuclei of the initial isotope, σ(Еγ) is the reaction cross section as a function of γ- quantum energy Еγ , Е th is the reaction threshold, Еγmах is the end-point energy of the bremsstrahlung spectrum, f (Еγmах, Еγ) is the function describing the X-ray spec- trum (computed with the use of the GEANT 4 package [4]). 2. 67Cu PRODUCTION PROCESS AT THE “ACCELERATOR” Sc&R Est, NSC KIPT 2.1. By the end of target irradiation at an accelerator, the contribution of short-lived (66Cu, 68Cu, 69Cu,63Zn, 69Zn) and long-lived (65Zn, 69Zn, 62Zn, 63Zn, 64Cu) radio- nuclides to the overall level of target radiation is hun- dreds times higher than the 67Cu radiation level. Be- sides, in the process of decay, the short-lived radionu- clides emit high-energy gammas, and that necessitates a substantial increase in the radiation shield thickness. Therefore, for the decay of short-lived isotopes, the ir- radiated target must be cooled in the accelerator vault. The optimum cooling period for natural target is deter- mined mainly by decay of the 62Zn, 63Zn isotopes, and makes 3 to 12 hours. After cooling, the target is delivered by means of a pneumatic tube from the accelerator vault to a transport container (TC) situated in a room above the vault. Then, by using an electric hoist, TC is transferred to an inlet box of the radiochemical laboratory. 2.2. The layout of the laboratory including the rooms and locations of the target on its way from TC to a tech- mailto:uvarov@kipt.kharkov.ua ISSN 1562-6016. ВАНТ. 2015. №6(100) 161 nological box TB (the points А1, А2, А6, А7,) is shown in Figure. The irradiated sample from TC is remotely discharged to a stationary box TB having iron and lead walls, where all the procedures of the 67Cu extraction are carried out (point A8). 70 69 Ф ФФ ФА8 А9 А7А6 А2 А10 А1 60 00 Room №16 Room №17 Room №18 Room №15 ТC ТB Layout of the radiochemical laboratory with the reference points The radiation level near the TB surface is deter- mined by the activity of the target being inside, and al- so, by a liquid radioactive waste (LRW) tank, located at the bottom of the box. The tank is filled weekly with LRW within one to three month period. 2.3. The specified permissible level of the equivalent dose rate (EDR) at the NSC KIPT makes 8.2 μSv/h. The expected EDR value was calculated at the following points of the plant (see Figure): А1 – the point near the transport container in the corridor; А2 – the point in a receiving chamber (room No 18); А6 – the point near the chamber for transporting the irradiated sample to the technological box (room No 17; А7 – the point behind the technological box (room No 17); А8 – the work seat before the technological box for operation with the 67Cu isotope (room No 16); А9 – the work seat before the 67Cu prepackage de- vice PD (clean room №16); А10 – the LRW tank. 3. ANALYSIS OF ISOTOPE CONTRIBUTION TO EDR The relationship between the absorbed dose rate caused by a point gamma source at a distance R, and the source activity M, expressed in mCi, is determined by the formula [3]: D • =2.35М·Кγ/R2, μGy/sec = 8.46М·Кγ/R2, mGy/h, (2) where Кγ[roent·cm2/(h·mCi)] is the specific gamma-ray constant, which shows the exposition dose rate pro- duced by the 1 mCi point γ-source at a distance of 1 cm for 1 hour. The refined values of the specific γ-ray con- stants for each radionuclide were calculated with due regard for its radiation spectrum and the number of gammas per 1 decay according to a BNL database [5]. The results are given in the Table 1. Since the quality factor of the 0.1 to 2 MeV gammas is equal to 1, then the equivalent dose H can be considered equal to the absorbed dose D. As it is evident from the Table 2, with consideration for the decay rate of the 67Cu and impurities, it is desir- able that the process operations should be performed, as expected, no sooner than 3 hours after irradiation. Then the 62Сu, 66Сu, 68Сu and 69Сu isotopes, having the half- life less than 10 minutes, would not contribute to the target radiation. At the 67Cu separation, other copper isotopes will be presented in the extract also. In particular, 64Сu (Т1/2=12.7 h) will transform to 64Ni. The concentration of 64Ni and 62Ni is expected to be comparable with the 67Сu content. In turn, the ratio of the 67Сu and 63Сu nu- clei in the extract was calculated by formula (1) ac- counting the percentage of the initial nuclei. The ratio was found to be 0.042 and 0.062 at an electron energy of 30 and 60 MeV, respectively. Taking into considera- tion the contributions of other reactions with the final- state copper isotopes, the ratio of the of 67Cu nuclei to the rest copper isotopes will be still less. At a 67Cu activity of 0.52 Ci and the target enriched in 68Zn up to 99%, as well as other conditions being hold true, the EDR value, ,H • determined by the 67Cu radiation, will be equal to 298 μSv/h. The contribution from 65Zn will be less than 0.25 μSv/h, and it may be neglected. The 63Zn (T1/2=38.1 min.) contribution just after EOB will be ~18 μSv/h. 3 hours later it will be 0.75 μSv/h. The contribution of other isotopes will be still less, and it may be also disregarded. As the gamma-radiation of the target includes many lines, to simplify the calculations, it is reasonable to unite the adjacent lines. From consideration of the in- tensity and energy of the gammas (see Table 2), it is apparent, that the lines of the 64 Cu, 63Zn, 65Zn isotopes with energy 1 to 1.5 MeV (20.8 % of radiation power) can be joined into one line, Еγ1=1.2 MeV. The lines of 64Cu, 63Zn, 62Zn, 65Zn, 69Zn with energies between 0.4 and 0.7 MeV (75.7 % of radiation power) can be joined into the other line, Еγ2=0.55 MeV. In this case, the radi- ation of 67Cu and the impurities with energy between 0.091 and 0.185 MeV, is no more than 3.5%. Table 3 lists the values of EDR ( ,H • μSv/h) behind the lead (iron) shield of thickness d at points Ai (see Figure), contributed by the 100 mCi 67Cu source based on the irradiated target from natural zinc, and also by the 0.52 Ci source based on the irradiated target made from 99% 68Zn-inriched material. In our calculations, the coefficients U and T, which characterize the protec- tive barrier type and the personnel occupancy in the given rooms, were taken from paper [6, 7] and put to equal 1. The operations with the natural target are as- sumed to be performed in 3 hours after irradiation. It is anticipated that the process of the 67Cu isotope production and the transfers of the irradiated target will be performed once for every week. In this case the aver- age dose received by an operator is estimated to be Нav= Н(А1)+Н(А2))+Н(А3)+Н(А6)+Н(А7) = 0.02+15.6 + 0.4+8=24 μSv. This being within the established limit (Table 4). ISSN 1562-6016. ВАНТ. 2015. №6(100) 162 Table 1 Isotope composition of irradiated Zn- target and their gamma-ray constant Isotope Еγ (MeV) Number of gammas per one decay Gamma-ray constant Кγi, Roent cm2/h·mCi γ-radiation composition, % 67Cu 0.091 0.22 0.09 0.57 0.093 0.57 0.25 1.58 0.185 0.22 0.21 1.33 64Cu 1.34 0.005 0.04 0.26 0.51 0.38 1.16 7.37 62Zn 0.041 0.25 - - 0.507 0.15 0.47 2.98 0.51 0.17 0.54 3.43 0.548 0.15 0.47 2.98 0.596 0.26 0.82 5.21 63Zn 0.51 1.85 5.54 35.18 0.669 0.085 0.36 2.29 1.412 0.008 0.06 0.38 0.961 0.07 0.43 2.73 65Zn 0.51 0.031 0.15 0.95 1.115 0.50 2.7 17.14 69mZn 0.439 1 2.45 15.56 0.574 0.03 0.01 0.06 Table 2 Partial activity of the isotopes and EDR from the irradiated Zn- target (R=0.9 m, unshielded) Isotope Half-life Target activity, mCi EDR, μSv/h By the EOB 3 hours after EOB Natural Enriched Natural Enriched Natural Enriched 67Cu 62.86 h 100 520 57.4 298.7 55.5 289 65Zn 243 days 24.3 0.085 72.3 0.25 72.3 0.25 69mZn 13.7 h 18.3 46.8 40.2 62Zn 9.26 h 186.6 386 308 64Cu 12.7 h 99.8 125.1 106.2 63Zn 0.635 h 1100 3.8 7340 19 278 0.72 Σ 1529 523.9 8023 318 853 290 Table 3 EDR produced by the 67Cu source behind lead (iron) shield of thickness d at reference point Аi ( 00 and 03 hours after irradiation) Point dPb, cm dFe, cm R, m 100 mCi 67Cu, natural Zn EDR μSv/h 0.52 Ci 67Cu, enriched Zn EDR (00), μSv/h EDR (03), μSv/h А1 14 0.9 0.4 0.033 <0.01 А2 14 0.5 1.3 0.1 <0.01 А7 6 0.9 774 91.6 <0.01 А8 5 0.9 51 3.9 <0.01 А6 5 9 7 0.5 165.2 15.8 47.6 12.7 1.23 3.73 <0.01 <0.01 <0.01 Table 4 Estimates of EDR being received by different organs of the operator at distance R during 67Cu packing procedures Point dPb, cm Organ, R, m EDR, μSv/h Natural zinc, 100 mCi Enriched zinc, 0.52 Ci А9 1 eyes, 0.5 bone marrow, 0.4 gonads, 0.4 hands, 0.08 1 1.5 1.5 37 5.2 7.8 7.6 1.9 А9 1.5 eyes, 0.5 bone marrow, 0.4 gonads, 0.4 hands, 0.08 0.08 0.12 0.12 3 0.4 0.6 0.6 15 ISSN 1562-6016. ВАНТ. 2015. №6(100) 163 4. ESTIMATION OF RADIATION SHIELD OF THE LRW TANK Table 5 gives the main isotopic composition and the partial activities of impurities in the water phase waste after the 67Cu extraction from the natural zinc-based target (12 hours after irradiation). The table gives also the dependence of the water drain on the period of its staying in the LRW tank. The next to last column of the table gives the partial activity of the weekly drain to the waste water phase, and the last column shows the max- imum radiation level at a distance of 0.9 m from the LRW tank. Table 5 Activity of isotopes produced in one drain run in 1, 2, 3 and 4 weeks after irradiation of natural zinc target, and the maximum radiation from the LRW tank three months later, at a distance of 0.9 m without shielding Isotope Target activity after 67Cu ex- traction 1st week after drain, mCi 2nd week after drain, mCi 3rd week after drain, mCi 4th week after drain, mCi Maximum activity in the LRW tank, mCi Maximum EDR of the LRW tank μSv/h 65Zn 24.28 23.84 23.36 22.9 22.44 260 787 69mZn 16.92 0.002 4·10-7 - - 16.92 43.3 63Zn 0.007 4·10-4 - - - 0.007 0.043 62Zn 149.2 3.8·10-4 - - - 149.2 308.4 Σ 190.4 23.842 23.36 22.9 22.44 426.1 113.8 The thickness of the LRW tank shield was calculat- ed in the same way like the calculation of the technolog- ical box shield. In view of change in the isotope activity ratio and the radiation spectra of the drain water phase, all radiation lines can be united into two lines, namely, 1.12 and 0.55 MeV. It is shown, that the required shield thickness is determined by the intensity of the nearby lines with Еγ =1.12 MeV, and is found to be 9 cm of lead. For the averaged 0.55 MeV line, the shield thick- ness will be 3.7 cm, and it can be disregarded. So the LRW tank must be discharged once in every week. Then the maximum EDR caused by the 1.12 MeV gammas at a distance of 0.9 m without shielding will be 71 μSv/h. In this case, the necessary attenuation factor will make up 17. The lead thickness of 5 cm will be sufficient to provide the EDR value no higher 4.1 μSv/h. CONCLUSIONS At treatment of the photonuclear target from natural zinc with 100 mCi activity in 67Cu, the technological box shield made from lead 5 cm thick (or 6 cm thick iron), as well as the 5 cm lead shield of the LRW tank provide the radiation environment, which meets stand- ard requirements. On the first day of the week produc- tion cycle, when performing procedures to transport the container with the irradiated target, and also, to extract 67Cu, the operator will receive a dose of 24 μSv. In sub- sequent four days, the average daily dose will make up 5.5 μSv, and the total annual dose will be 1.26 mSv. That is much less than the permissible dose limit of 20 mSv. Under those conditions, the radiation risk will be no more than 7·10-5. In the case of the enriched zinc target of the same weight with activity 520 mCi, provided by the same irradiation mode, the dose received by the operator dur- ing packing will be distributed as follows: 4.3 μSv/day for bone marrow and gonads, and 110 μSv/day for hands (at a norm of 340 μSv/day). With increase up to 2 cm in the lead thickness of the container for the separated 67 Cu product, the dose ob- tained by the hands will be decreased down to 8.5 μSv/day, and the radiation risk will amount 5.6·10-5. At the use of the enriched target, the productivity of 67Cu is by a factor of 5.2 higher than that for a target of natural composition. Considering that 1 gram of en- riched 68Zn and one hour of the accelerator operation cost $500/g and $200/hour, respectively, the increase in the yield of the target isotope for a 30-hour cycle will fully compensate the cost of the target of enriched com- position. REFERENCES 1. Manual for reactor produced radioisotopes. IAEA – TECDOC - 1340, 2003. 2. V. Uvarov, N. Ayzatskiy, N. Dikiy, A. Dovbnya, et al. Comparison of Cu-67 Production at Cyclotron and Electron Accelerator // Conf. on Cyclotrons and their Applications (Cyclotron, Giardini Naxos, Ita- ly). 2007, p. 224-226. 3. Health Physics / Ed. H.G. Gusev. Moscow: “Ehnergoatomizdat”, 1989. 4. http//:geant 4. cern.ch. 5. www. Nu Dat 2.6. 6. Basic sanitary rules of radiation safety ensuring in Ukraine // National sanitary regulations. 6.177- 2005–09-02. Kiev, 2005. 7. Unified rules of organization and safe operation of radio-processing installations. (Unified gamma- electron rules). Moscow, 1988. Article received 26.10.2015 ISSN 1562-6016. ВАНТ. 2015. №6(100) 164 ОПТИМИЗАЦИЯ УСЛОВИЙ ФОТОЯДЕРНОГО ПРОИЗВОДСТВА 67Cu А.Н. Довбня, М.А. Должек, Г.Д. Пугачев, О.А. Репихов, А.В. Торговкин, В.Л. Уваров, В.С. Шестакова, Б.И. Шраменко Радиофармпрепараты на основе изотопа 67Cu широко используются в иммунотерапии. В сообщении про- анализированы условия его производства на ускорителе электронов по реакции 68Zn(γ,n)67Cu в отношении выхода целевого продукта, а также горячих примесей и радиационных рисков. Рассмотрены варианты тех- нологической мишени массой 40 г из цинка природного состава и обогащенного до 99% по изотопу 68Zn, активированной тормозным излучением с граничной энергией 30 и 60 МэВ. Показано, что при использова- нии обогащенной мишени радиационный риск снижается до 10-4, а также значительно уменьшается объем процедур с отходами. ОПТИМІЗАЦІЯ УМОВ ФОТОЯДЕРНОГО ВИРОБНИЦТВА 67Cu А.М. Довбня, М.А. Должек, Г.Д. Пугачев, О.О. Репіхов, О.В. Торговкін, В.Л. Уваров, В.С. Шестакова, Б.І. Шраменко Радіофармпрепарати на основі ізотопу 67Cu широко використовуються в імунотерапії. У повідомленні проаналізовані умови його виробництва на прискорювачі електронів за реакцією 68Zn(γ,n)67Cu відносно ви- ходу цільового продукту, а також гарячих домішок і радіаційних ризиків. Розглянуто варіанти технологічної мішені масою 40 г із цинку природного складу і збагаченого до 99% за ізотопом 68Zn, активованою гальмів- ним випромінюванням із граничною енергією 30 і 60 МеВ. Показано, що при використанні збагаченої міше- ні радіаційний ризик знижується до 10-4, а також значно зменшується обсяг процедур з відходами. INTRODUCTION 1. MAIN REACTIONS 2. 67Cu PRODUCTION PROCESS AT THE “ACCELERATOR” Sc&R Est, NSC KIPT 3. ANALYSIS OF ISOTOPE CONTRIBUTION TO EDR EDR, μSv/h Isotope 3 hours after EOB Σ By the EOB Point Point Isotope 4. ESTIMATION OF RADIATION SHIELD OF THE LRW TANK
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institution Digital Library of Periodicals of National Academy of Sciences of Ukraine
issn 1562-6016
language English
last_indexed 2025-12-07T15:28:42Z
publishDate 2015
publisher Національний науковий центр «Харківський фізико-технічний інститут» НАН України
record_format dspace
spelling Dovbnya, A.N.
Dolzhek, M.A.
Pugachev, G.D.
Repikhov, O.A.
Torgovkin, A.V.
Uvarov, V.L.
Shestakova, V.S.
Shramenko, B.I.
2017-01-20T18:10:32Z
2017-01-20T18:10:32Z
2015
Optimization of conditions for ⁶⁷Cu photonuclear production / A.N. Dovbnya, M.A. Dolzhek, G.D. Pugachev, O.A. Repikhov, A.V. Torgovkin, V.L. Uvarov, V.S. Shestakova, B.I. Shramenko // Вопросы атомной науки и техники. — 2015. — № 6. — С. 160-164. — Бібліогр.: 7 назв. — англ.
1562-6016
PACS: 07.85.-m, 81.40wx, 87.53-j, 87.53Wz
https://nasplib.isofts.kiev.ua/handle/123456789/112372
Radiopharmaceuticals based on the ⁶⁷Cu isotope have found wide use in immunotherapy. The present paper analyzes the conditions of ⁶⁷Cu production by the ⁶⁸Zn(γ,p) ⁶⁷Cu reaction at an electron accelerator in relation to the target isotope and hot impurities yield, as well as the radiation risks. Consideration has been given to some variants of the technological target 40 g in weight made from natural zinc, and one enriched up to 99% in the ⁶⁸Zn isotope. The target exposition to bremsstrahlung with end-point energy 30 and 60 MeV was studied. It has been found that the use of enriched target results in reduction of both the radiation risk (down to 10⁻⁴) and the scope of waste han-dling procedures.
Радіофармпрепарати на основі ізотопу ⁶⁷Cu широко використовуються в імунотерапії. У повідомленні проаналізовані умови його виробництва на прискорювачі електронів за реакцією ⁶⁸Zn(γ,n)⁶⁷Cu відносно виходу цільового продукту, а також гарячих домішок і радіаційних ризиків. Розглянуто варіанти технологічної мішені масою 40 г із цинку природного складу і збагаченого до 99% за ізотопом ⁶⁸Zn, активованою гальмівним випромінюванням із граничною енергією 30 і 60 МеВ. Показано, що при використанні збагаченої мішені радіаційний ризик знижується до 10⁻⁴, а також значно зменшується обсяг процедур з відходами.
Радиофармпрепараты на основе изотопа ⁶⁷Cu широко используются в иммунотерапии. В сообщении проанализированы условия его производства на ускорителе электронов по реакции ⁶⁸Zn(γ,n)⁶⁷Cu в отношении выхода целевого продукта, а также горячих примесей и радиационных рисков. Рассмотрены варианты технологической мишени массой 40 г из цинка природного состава и обогащенного до 99% по изотопу ⁶⁸Zn, активированной тормозным излучением с граничной энергией 30 и 60 МэВ. Показано, что при использовании обогащенной мишени радиационный риск снижается до 10⁻⁴, а также значительно уменьшается объем процедур с отходами.
en
Національний науковий центр «Харківський фізико-технічний інститут» НАН України
Вопросы атомной науки и техники
Применение ядерных методов
Optimization of conditions for ⁶⁷Cu photonuclear production
Оптимізація умов фотоядерного виробництва ⁶⁷Cu
Оптимизация условий фотоядерного производства ⁶⁷Cu
Article
published earlier
spellingShingle Optimization of conditions for ⁶⁷Cu photonuclear production
Dovbnya, A.N.
Dolzhek, M.A.
Pugachev, G.D.
Repikhov, O.A.
Torgovkin, A.V.
Uvarov, V.L.
Shestakova, V.S.
Shramenko, B.I.
Применение ядерных методов
title Optimization of conditions for ⁶⁷Cu photonuclear production
title_alt Оптимізація умов фотоядерного виробництва ⁶⁷Cu
Оптимизация условий фотоядерного производства ⁶⁷Cu
title_full Optimization of conditions for ⁶⁷Cu photonuclear production
title_fullStr Optimization of conditions for ⁶⁷Cu photonuclear production
title_full_unstemmed Optimization of conditions for ⁶⁷Cu photonuclear production
title_short Optimization of conditions for ⁶⁷Cu photonuclear production
title_sort optimization of conditions for ⁶⁷cu photonuclear production
topic Применение ядерных методов
topic_facet Применение ядерных методов
url https://nasplib.isofts.kiev.ua/handle/123456789/112372
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