Isotope Preparations Generated with Thermal Neutron Irradiation

Isotope preparations belonging to this group are generated with the (n, Y) nuclear reaction, followed by dissolution and chemical processing of the target. Radiochemical separation is needed only in those cases when other atoms in the compound besides the desired one are highly activated. The products typically con­tain carriers; for this reason, their specific activity is relatively low.

Among the production methods described in the following section, the first two technologies are very simple because, due to the homogeneous isotope composition and ideal chemical composition of the target, only the target nuclide is generated during irradiation without contaminating radionuclides, and so radiochemical sepa­ration is not needed.

The 90Y radionuclide (Table 8.5) with its energy belongs to the group of high — range beta-emitting radionuclides: its penetration in tissues of the living organ is 1—2 cm, so it is suitable for the therapeutic treatment of bone metastases of similar size. The organ-specific behavior of this radionuclide—e. g., penetration of 90Y radionuclide into bone metastases—is ensured by adding ethylene diamine methy­lene phosphonate (EDTMP) to the radionuclide at the treatment site and the formed

Подпись: Table 8.5 Preparation of 90Y-Labeled YCl3 Nuclear parameters Half-life: 64 h. Decay mode and energy: [3_ (keV) 2281. Utilization Used in nuclear medicine for isotope therapy, for treating inflammations and bone metastases. Its high-energy [3_-radiation is absorbed within a distance of couple of centimeters in the body tissues, while the emitted energy has inflammation and pain reduction effect. Target material Yttrium oxide, 90Y2O3, with natural isotope abundance. Target irradiation In research reactor with thermal neutrons, for some days. Primary nuclear reaction 89Y(n,Y)90Y. Nuclear reactions resulting in None. Note, however, that activation of the chemical contaminating nuclides impurities present in the target can generate contaminating radionuclides. Target processing Dissolution in diluted hydrochloric acid with light heating. Chemical processing For eliminating hydrochloric acid, evaporation to dry. Dissolution of the dry residue in highly diluted hydrochloric acid. pH adjustment to 2—3 with 1 mol/dm3 HCl. Product finishing Adjustment of radioactive concentration, dispensing to the ordered number of ampoules and steam sterilization in an autoclave. Other ways of production By extraction of fission products of uranium irradiation with a nuclear reaction of: U(n,f) ~90Sr!90Y (yield: 5.9%)

complex is intravenously injected to the patient. Typical activity of the injection is 17.5—37 MBq. The total activity of the production batches is approximately 370 MBq.

The 153Sm radionuclide (shown in the Table 8.6) with its energy belongs to the group of low-range beta-emitting radionuclides. Its penetration in tissues of the living organ is 1 —2 mm, so it is suitable for the therapeutic treatment of bone metastases of similar size. The organ-specific behavior of this radionuclide—e. g., penetration of 153Sm radionuclide into bone metastases—is ensured by adding EDTMP to the radionuclide on the treatment site, and the formed complex is intra­venously injected into the patient. The typical activity of the injection is 150—260 MBq. The total activity of the production batches is approximately 2600 MBq.

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Other radionuclides belonging to the group that does not require isotope separa­tion are 186Re, 166Ho 169Yb, 165Dy, 177Lu, 89Sr, 59Fe, and 198Au (for medical appli­

Table 8.6 Preparation of 153Sm-Labeled SmCl3

Nuclear parameters

Half-life: 46 h.

Decay mode and energy: [3_ (keV) 705 and y (keV) 103 and 635.

Utilization

Used in nuclear medicine for isotope therapy, for treating inflammations and bone metastases.

Its low-energy [3_-radiation is absorbed within a distance of a few millimeters in the body tissues, while the emitted energy has inflammation and pain reduction effects.

Target material

Samarium oxide, 152Sm2O3 enriched to 99% abundance.

Target irradiation

In a research reactor with thermal neutrons, for some days.

Primary nuclear reaction

152Sm(n, Y)153Sm.

Nuclear reactions resulting in

None. Note, however, that activation of the chemical

contaminating nuclides

impurities present in the target can generate contaminating radionuclides.

Target processing

Dissolution in diluted hydrochloric acid with light heating.

Chemical processing

For eliminating hydrochloric acid, evaporation to dry. Dissolution of the dry residue in highly diluted hydrochloric acid. pH adjustment to 5—6 with 1 mol/dm3 HCl.

Product finishing

Adjustment of radioactive concentration, dispensing to the ordered number of ampoules and steam sterilization in an autoclave.

Other ways of production

Not known.

The following two production procedures (51Cr and 82Br) are examples of hav­ing multiple chemical elements present in the target. Consequently, the activation of the target, in addition to the target isotope, results in contaminating radionuclide of significant activity, thus requiring subsequent radiochemical separation.

In medical applications, the typical injected activity of 51Cr administered to patient is 10—18.5 MBq, so typical batch activity of the production is around 370 MBq.

In industry, the 51Cr radioisotope (shown in Table 8.7) is widely used for tracer investigation of metallurgical processes and for studying corrosion processes due to the fact that chromium is an important component of the iron — and steel-based structures.

The 82Br radioisotope (see Table 8.8), as a halogen element, can be used as a tracer isotope for halogenation of various industrial components. It has high-energy gamma radiation; therefore, it can be detected outside industrial equipment or pipe­lines. Due to its short half-life, it decays rapidly after the investigation.

The most important industrial application of the 82Br radioisotope is the leakage test of oil pipelines. This 82Br-labeled methyl bromide with an activity of

Nuclear parameters Utilization

 

Half-life: 28 days.

Decay mode and energy: EX (100%) and y (keV) 323.

Applied in medical diagnosis for labeling intravenously injectable blood plasma preparations. The labeled preparations are used for hematological tests, e. g., blood volume determination.

Enriched (86%) barium chromate, 50BaCrO4. The target is not Cr2O3 because it cannot be dissolved easily. Although contaminating radionuclides generated from Ba do not have very high activity, radiochemical separation is necessary.

In the research reactor, with thermal neutrons, for some months.

50Cr(n, Y)51Cr.

59Co(n, Y)60Co, 58Fe(n, Y)59Fe, 130Ba(n, Y)131Ba, 132Ba(n, Y)133Ba, and 138Ba(n, Y)139Ba.

In dilute alkaline, adding hydrogen peroxide under boiling to facilitate dissolution and formation of trivalent Cr31.

Acidification by adding diluted hydrochloric acid.

Boiling. Precipitation of Ba ions by adding Na2SO4 followed by filtration.

Forming Na chromate by neutralizing the solution with diluted sodium hydroxide. pH adjustment to 6—8.

Adjustment of radioactive concentration, dispensing to the ordered number of ampoules and steam sterilization in an autoclave.

a. Neutron irradiation of metallic chromium and chemical processing.

b. Vanadium irradiation with deuteron by the following nuclear reactions: 50V (d, n) 51Cr or 51V (d,2n) 51Cr

c. High specific activity can be reached by applying the Szilard—Chalmers effect on chromium compounds with natural abundance (Section 6.4).

d. It is also produced in the form of a 51Cr—EDTA complex.

 

Target material

 

Target irradiation

Primary nuclear reaction Nuclear reactions resulting in contaminating nuclides Target processing

 

Radiochemical separation

 

Chemical processing Product finishing

 

Other ways of production

 

37—74 MBq is injected into the pipeline, and after passing the radioactive cloud, leakage spots are identified using a radiation detector built into a “pig,” together with a distance meter running along the inside of the pipeline. The radiation detec­tor identifies the spots where radioactive tracer oozed outside the pipeline.

In the environment, 82Br is the tracer of choice for tracing surface water and groundwater movements, since the nonadsorbing character of halogens on solid components of soils allows tracking of the movement of flowing waters. The chem­ical form of Na82Br meets this requirement.

 

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Table 8.8 Preparation of 82Br-Labeled NaBr

Nuclear parameters

Half-life: 35 h.

Decay mode and energy: [3_ (100%) and y (keV) 55, 619, 698, 777, 828, 1044, 1317, 1475.

Utilization

Due to its high gamma energy, this radioisotope is mainly used for investigating industrial and environmental processes.

Target material

Potassium bromide (KBr) with natural abundance (49%). Because K is activated in addition to Br, the generated 42K and 80Br radioisotope must be separated from the product.

Target irradiation

In a research reactor with thermal neutrons, for some days.

Primary nuclear reaction

81Br(n, Y)82Br.

Nuclear reactions resulting in

41K(n, Y)42K.

contaminating nuclides

79Br(n, Y)80Br.

Target processing

Dissolution of 42K82Br in water.

Radiochemical separation

Passing the solution through ion-exchange resin in order to exchange K1 ions to Na1 ions. Due to its short half­life (17.6 min) 80Br can be cooled from radionuclides.

Chemical processing

Dissolution of the eluent of the cation resin in 1 mol/dm3 NaOH. Adjusting the pH to 6—8 with diluted NaOH.

Product finishing

Adjustment of radioactive concentration, dispensing to the ordered number of ampoules.

Other ways of production

If NH482Br is chosen as the irradiated target, no ion exchange is necessary, but this target material is less stable.