Cyclotron production of 101 Pd/ 101m Rh radionuclide generator for radioimmunotherapy
101m Rh is one of such radionuclides that has been considered as a potential candidate for targeted radiotherapeutic use, due to its nuclear decay and chemical properties. Electrodeposition of rhodium metal on a copper backing was performed in acidic sulphate. The target was bombarded with a current...
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Veröffentlicht in: | Kerntechnik (1987) 2011-05, Vol.76 (2), p.131-135 |
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container_title | Kerntechnik (1987) |
container_volume | 76 |
creator | Enferadi, M. Sadeghi, M. Ensaf, M. |
description | 101m
Rh is one of such radionuclides that has been considered as a potential candidate for targeted radiotherapeutic use, due to its nuclear decay and chemical properties. Electrodeposition of rhodium metal on a copper backing was performed in acidic sulphate. The target was bombarded with a current intensity of 120 μA (E
p
= 29 → 25 MeV) for 30 min (60 μAh). Radiochemical methods were investigated to optimize the production of no-carrier-added
101
Pd/
101m
Rh. The use of a cyclotron target with radiochemical processes (i.e. electrodeposition, electrodissolution and ion-exchange column chromatography) were carried out to produce this radionuclide in high-specific activity and radiochemical form suitable for radiopharmaceutical syntheses. |
doi_str_mv | 10.3139/124.110118 |
format | Article |
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Rh is one of such radionuclides that has been considered as a potential candidate for targeted radiotherapeutic use, due to its nuclear decay and chemical properties. Electrodeposition of rhodium metal on a copper backing was performed in acidic sulphate. The target was bombarded with a current intensity of 120 μA (E
p
= 29 → 25 MeV) for 30 min (60 μAh). Radiochemical methods were investigated to optimize the production of no-carrier-added
101
Pd/
101m
Rh. The use of a cyclotron target with radiochemical processes (i.e. electrodeposition, electrodissolution and ion-exchange column chromatography) were carried out to produce this radionuclide in high-specific activity and radiochemical form suitable for radiopharmaceutical syntheses.</description><identifier>ISSN: 0932-3902</identifier><identifier>EISSN: 2195-8580</identifier><identifier>DOI: 10.3139/124.110118</identifier><language>eng</language><ispartof>Kerntechnik (1987), 2011-05, Vol.76 (2), p.131-135</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c768-1e6f3e165eee119613d7c50dd8dc931d0f2abbc16f7db1fd59800e8252212fe33</citedby><cites>FETCH-LOGICAL-c768-1e6f3e165eee119613d7c50dd8dc931d0f2abbc16f7db1fd59800e8252212fe33</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27922,27923</link.rule.ids></links><search><creatorcontrib>Enferadi, M.</creatorcontrib><creatorcontrib>Sadeghi, M.</creatorcontrib><creatorcontrib>Ensaf, M.</creatorcontrib><title>Cyclotron production of 101 Pd/ 101m Rh radionuclide generator for radioimmunotherapy</title><title>Kerntechnik (1987)</title><description>101m
Rh is one of such radionuclides that has been considered as a potential candidate for targeted radiotherapeutic use, due to its nuclear decay and chemical properties. Electrodeposition of rhodium metal on a copper backing was performed in acidic sulphate. The target was bombarded with a current intensity of 120 μA (E
p
= 29 → 25 MeV) for 30 min (60 μAh). Radiochemical methods were investigated to optimize the production of no-carrier-added
101
Pd/
101m
Rh. The use of a cyclotron target with radiochemical processes (i.e. electrodeposition, electrodissolution and ion-exchange column chromatography) were carried out to produce this radionuclide in high-specific activity and radiochemical form suitable for radiopharmaceutical syntheses.</description><issn>0932-3902</issn><issn>2195-8580</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><recordid>eNotkM1qwzAQhEVpoSbNpU-gc8GJVopk6VhM_yDQUtKzsaVV42JbQbYPfvsqTQeGWXZgDh8h98A2AoTZAt9tABiAviIZByNzLTW7JhkzgufCMH5L1uP4w5IUL-SOZeSrXGwXphgGeorBzXZq0xk8TTv0w23P2dPPI421S81su9Yh_cYBYz2FSH3yX9X2_TyE6Zj-p-WO3Pi6G3H9nytyeH46lK_5_v3lrXzc57ZQOgdUXiAoiYgARoFwhZXMOe2sEeCY53XTWFC-cA14J41mDDWXnAP3KMSKPFxmbQzjGNFXp9j2dVwqYNUZSZWQVBck4hfTy1K7</recordid><startdate>20110501</startdate><enddate>20110501</enddate><creator>Enferadi, M.</creator><creator>Sadeghi, M.</creator><creator>Ensaf, M.</creator><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20110501</creationdate><title>Cyclotron production of 101 Pd/ 101m Rh radionuclide generator for radioimmunotherapy</title><author>Enferadi, M. ; Sadeghi, M. ; Ensaf, M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c768-1e6f3e165eee119613d7c50dd8dc931d0f2abbc16f7db1fd59800e8252212fe33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Enferadi, M.</creatorcontrib><creatorcontrib>Sadeghi, M.</creatorcontrib><creatorcontrib>Ensaf, M.</creatorcontrib><collection>CrossRef</collection><jtitle>Kerntechnik (1987)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Enferadi, M.</au><au>Sadeghi, M.</au><au>Ensaf, M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cyclotron production of 101 Pd/ 101m Rh radionuclide generator for radioimmunotherapy</atitle><jtitle>Kerntechnik (1987)</jtitle><date>2011-05-01</date><risdate>2011</risdate><volume>76</volume><issue>2</issue><spage>131</spage><epage>135</epage><pages>131-135</pages><issn>0932-3902</issn><eissn>2195-8580</eissn><abstract>101m
Rh is one of such radionuclides that has been considered as a potential candidate for targeted radiotherapeutic use, due to its nuclear decay and chemical properties. Electrodeposition of rhodium metal on a copper backing was performed in acidic sulphate. The target was bombarded with a current intensity of 120 μA (E
p
= 29 → 25 MeV) for 30 min (60 μAh). Radiochemical methods were investigated to optimize the production of no-carrier-added
101
Pd/
101m
Rh. The use of a cyclotron target with radiochemical processes (i.e. electrodeposition, electrodissolution and ion-exchange column chromatography) were carried out to produce this radionuclide in high-specific activity and radiochemical form suitable for radiopharmaceutical syntheses.</abstract><doi>10.3139/124.110118</doi><tpages>5</tpages></addata></record> |
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issn | 0932-3902 2195-8580 |
language | eng |
recordid | cdi_crossref_primary_10_3139_124_110118 |
source | De Gruyter journals |
title | Cyclotron production of 101 Pd/ 101m Rh radionuclide generator for radioimmunotherapy |
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