Evaluation of Bifunctional Chelates for the Development of Gallium-Based Radiopharmaceuticals
Ga radioisotopes, including the generator-produced positron-emitting isotope 68Ga (t 1/2 = 68 min), are of increasing interest for the development of new radiopharmaceuticals. Bifunctional chelates (BFCs) that can be efficiently radiolabeled with Ga to yield complexes with good in vivo stability are...
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description | Ga radioisotopes, including the generator-produced positron-emitting isotope 68Ga (t 1/2 = 68 min), are of increasing interest for the development of new radiopharmaceuticals. Bifunctional chelates (BFCs) that can be efficiently radiolabeled with Ga to yield complexes with good in vivo stability are needed. To this end, we undertook a systematic comparison of four BFCs containing different chelating moieties: two novel BFCs, p-NO2-Bn-Oxo (1-oxa-4,7,10-triazacyclododecane-4,7,10-triacetic acid) and p-NO2-Bn-PCTA (3,6,9,15-tetraazabicyclo [9.3.1]pentadeca-1(15),11,13-triene-3,6,9-triacetic acid), and two more commonly used BFCs, p-NO2-Bn-DOTA (1,4,7,10-tetraazacyclododecane-1,4,7,10-tetraacetic acid) and p-NO2-Bn-NOTA (1,4,7-triazacyclononane-1,4,7-triacetic acid). Each BFC was compared with respect to radiolabeling conditions, radiochemical yield, stability, and in vivo clearance properties. p-NO2-Bn-PCTA, p-NO2-Bn-Oxo, and p-NO2-Bn-NOTA were all more efficiently radiolabeled with Ga compared to p-NO2-Bn-DOTA. p-NO2-Bn-DOTA required longer reaction time, higher concentrations of BFC, or heating to obtain equivalent radiochemical yields. Better stability was observed for p-NO2-Bn-NOTA and p-NO2-Bn-PCTA compared to p-NO2-Bn-DOTA and p-NO2-Bn-Oxo, especially with respect to transmetalation to transferrin. Ga-radiolabled p-NO2-Bn-Oxo was found to be kinetically labile and therefore unstable in vivo. Ga-radiolabeled p-NO2-Bn-NOTA and p-NO2-Bn-PCTA were relatively inert, while Ga-radiolabeled p-NO2-Bn-DOTA had intermediate stability, losing >20% of Ga in less than one hour when incubated with apo-transferrin. Similar stability differences were seen when incubating at pH 2. In vivo PET imaging and biodistribution studies in mice showed that 68Ga-radiolabeled p-NO2-Bn-PCTA, p-NO2-Bn-NOTA, and p-NO2-Bn-DOTA all cleared through the kidneys. While there was no statistical difference in the biodistribution results of 68Ga-radiolabeled p-NO2-Bn-PCTA and p-NO2-Bn-DOTA, 68Ga-radiolabeled p-NO2-Bn-NOTA cleared more rapidly from blood and muscle tissue but retained at up to 5 times higher activity in the kidneys. |
doi_str_mv | 10.1021/bc900443a |
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Bifunctional chelates (BFCs) that can be efficiently radiolabeled with Ga to yield complexes with good in vivo stability are needed. To this end, we undertook a systematic comparison of four BFCs containing different chelating moieties: two novel BFCs, p-NO2-Bn-Oxo (1-oxa-4,7,10-triazacyclododecane-4,7,10-triacetic acid) and p-NO2-Bn-PCTA (3,6,9,15-tetraazabicyclo [9.3.1]pentadeca-1(15),11,13-triene-3,6,9-triacetic acid), and two more commonly used BFCs, p-NO2-Bn-DOTA (1,4,7,10-tetraazacyclododecane-1,4,7,10-tetraacetic acid) and p-NO2-Bn-NOTA (1,4,7-triazacyclononane-1,4,7-triacetic acid). Each BFC was compared with respect to radiolabeling conditions, radiochemical yield, stability, and in vivo clearance properties. p-NO2-Bn-PCTA, p-NO2-Bn-Oxo, and p-NO2-Bn-NOTA were all more efficiently radiolabeled with Ga compared to p-NO2-Bn-DOTA. p-NO2-Bn-DOTA required longer reaction time, higher concentrations of BFC, or heating to obtain equivalent radiochemical yields. Better stability was observed for p-NO2-Bn-NOTA and p-NO2-Bn-PCTA compared to p-NO2-Bn-DOTA and p-NO2-Bn-Oxo, especially with respect to transmetalation to transferrin. Ga-radiolabled p-NO2-Bn-Oxo was found to be kinetically labile and therefore unstable in vivo. Ga-radiolabeled p-NO2-Bn-NOTA and p-NO2-Bn-PCTA were relatively inert, while Ga-radiolabeled p-NO2-Bn-DOTA had intermediate stability, losing >20% of Ga in less than one hour when incubated with apo-transferrin. Similar stability differences were seen when incubating at pH 2. In vivo PET imaging and biodistribution studies in mice showed that 68Ga-radiolabeled p-NO2-Bn-PCTA, p-NO2-Bn-NOTA, and p-NO2-Bn-DOTA all cleared through the kidneys. While there was no statistical difference in the biodistribution results of 68Ga-radiolabeled p-NO2-Bn-PCTA and p-NO2-Bn-DOTA, 68Ga-radiolabeled p-NO2-Bn-NOTA cleared more rapidly from blood and muscle tissue but retained at up to 5 times higher activity in the kidneys.</description><identifier>ISSN: 1043-1802</identifier><identifier>EISSN: 1520-4812</identifier><identifier>DOI: 10.1021/bc900443a</identifier><identifier>PMID: 20175523</identifier><language>eng</language><publisher>United States: American Chemical Society</publisher><subject>Animals ; Chelating Agents - chemistry ; Chelating Agents - pharmacokinetics ; Comparative analysis ; Gallium Radioisotopes - chemistry ; Gallium Radioisotopes - pharmacokinetics ; Kidneys ; Kinetics ; Male ; Mice ; Mice, Inbred Strains ; Molecular Structure ; Organometallic Compounds - chemical synthesis ; Organometallic Compounds - chemistry ; Organometallic Compounds - pharmacokinetics ; Positron-Emission Tomography ; Radioisotopes ; Radiopharmaceuticals - chemical synthesis ; Radiopharmaceuticals - chemistry ; Radiopharmaceuticals - pharmacokinetics ; Rodents ; Tissue Distribution ; Tissues</subject><ispartof>Bioconjugate chemistry, 2010-03, Vol.21 (3), p.531-536</ispartof><rights>Copyright © 2010 American Chemical Society</rights><rights>Copyright American Chemical Society Mar 17, 2010</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a374t-61a47050251fc146f3cbbc75b1db0ebfc2f6bdd8b32b6d3b631cda32a65d54413</citedby><cites>FETCH-LOGICAL-a374t-61a47050251fc146f3cbbc75b1db0ebfc2f6bdd8b32b6d3b631cda32a65d54413</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://pubs.acs.org/doi/pdf/10.1021/bc900443a$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/bc900443a$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>314,780,784,2763,27074,27922,27923,56736,56786</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20175523$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ferreira, Cara L</creatorcontrib><creatorcontrib>Lamsa, Eric</creatorcontrib><creatorcontrib>Woods, Michael</creatorcontrib><creatorcontrib>Duan, Yin</creatorcontrib><creatorcontrib>Fernando, Pasan</creatorcontrib><creatorcontrib>Bensimon, Corinne</creatorcontrib><creatorcontrib>Kordos, Myra</creatorcontrib><creatorcontrib>Guenther, Katharina</creatorcontrib><creatorcontrib>Jurek, Paul</creatorcontrib><creatorcontrib>Kiefer, Garry E</creatorcontrib><title>Evaluation of Bifunctional Chelates for the Development of Gallium-Based Radiopharmaceuticals</title><title>Bioconjugate chemistry</title><addtitle>Bioconjugate Chem</addtitle><description>Ga radioisotopes, including the generator-produced positron-emitting isotope 68Ga (t 1/2 = 68 min), are of increasing interest for the development of new radiopharmaceuticals. Bifunctional chelates (BFCs) that can be efficiently radiolabeled with Ga to yield complexes with good in vivo stability are needed. To this end, we undertook a systematic comparison of four BFCs containing different chelating moieties: two novel BFCs, p-NO2-Bn-Oxo (1-oxa-4,7,10-triazacyclododecane-4,7,10-triacetic acid) and p-NO2-Bn-PCTA (3,6,9,15-tetraazabicyclo [9.3.1]pentadeca-1(15),11,13-triene-3,6,9-triacetic acid), and two more commonly used BFCs, p-NO2-Bn-DOTA (1,4,7,10-tetraazacyclododecane-1,4,7,10-tetraacetic acid) and p-NO2-Bn-NOTA (1,4,7-triazacyclononane-1,4,7-triacetic acid). Each BFC was compared with respect to radiolabeling conditions, radiochemical yield, stability, and in vivo clearance properties. p-NO2-Bn-PCTA, p-NO2-Bn-Oxo, and p-NO2-Bn-NOTA were all more efficiently radiolabeled with Ga compared to p-NO2-Bn-DOTA. p-NO2-Bn-DOTA required longer reaction time, higher concentrations of BFC, or heating to obtain equivalent radiochemical yields. Better stability was observed for p-NO2-Bn-NOTA and p-NO2-Bn-PCTA compared to p-NO2-Bn-DOTA and p-NO2-Bn-Oxo, especially with respect to transmetalation to transferrin. Ga-radiolabled p-NO2-Bn-Oxo was found to be kinetically labile and therefore unstable in vivo. Ga-radiolabeled p-NO2-Bn-NOTA and p-NO2-Bn-PCTA were relatively inert, while Ga-radiolabeled p-NO2-Bn-DOTA had intermediate stability, losing >20% of Ga in less than one hour when incubated with apo-transferrin. Similar stability differences were seen when incubating at pH 2. In vivo PET imaging and biodistribution studies in mice showed that 68Ga-radiolabeled p-NO2-Bn-PCTA, p-NO2-Bn-NOTA, and p-NO2-Bn-DOTA all cleared through the kidneys. While there was no statistical difference in the biodistribution results of 68Ga-radiolabeled p-NO2-Bn-PCTA and p-NO2-Bn-DOTA, 68Ga-radiolabeled p-NO2-Bn-NOTA cleared more rapidly from blood and muscle tissue but retained at up to 5 times higher activity in the kidneys.</description><subject>Animals</subject><subject>Chelating Agents - chemistry</subject><subject>Chelating Agents - pharmacokinetics</subject><subject>Comparative analysis</subject><subject>Gallium Radioisotopes - chemistry</subject><subject>Gallium Radioisotopes - pharmacokinetics</subject><subject>Kidneys</subject><subject>Kinetics</subject><subject>Male</subject><subject>Mice</subject><subject>Mice, Inbred Strains</subject><subject>Molecular Structure</subject><subject>Organometallic Compounds - chemical synthesis</subject><subject>Organometallic Compounds - chemistry</subject><subject>Organometallic Compounds - pharmacokinetics</subject><subject>Positron-Emission Tomography</subject><subject>Radioisotopes</subject><subject>Radiopharmaceuticals - chemical synthesis</subject><subject>Radiopharmaceuticals - chemistry</subject><subject>Radiopharmaceuticals - pharmacokinetics</subject><subject>Rodents</subject><subject>Tissue Distribution</subject><subject>Tissues</subject><issn>1043-1802</issn><issn>1520-4812</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp90dtKw0AQBuBFFK3VC19AgiDqRXRnD0lzaesRCoLopYTZE41sujWbFHx7U-oBFLyaHfj4F-Yn5ADoOVAGF0oXlArBcYMMQDKaihGwzf5NBU9hRNkO2Y3xlVJawIhtkx1GIZeS8QF5uV6i77CtwjwJLhlXrpvr1YY-mcysx9bGxIUmaWc2ubJL68OitvN2hW_R-6qr0zFGa5JHNFVYzLCpUduurTT6uEe2XD_s_ucckueb66fJXTp9uL2fXE5T5Llo0wxQ5FRSJsFpEJnjWimdSwVGUaucZi5TxowUZyozXGUctEHOMJNGCgF8SE7WuYsmvHU2tmVdRW29x7kNXSxzKaTIuWC9PP1XgigKYEUueE-PftHX0DX9YWLJIIOCglyhszXSTYixsa5cNFWNzXsJtFyVU36X09vDz8BO1dZ8y682enC8Bqjjz2d_gz4APxOVGg</recordid><startdate>20100317</startdate><enddate>20100317</enddate><creator>Ferreira, Cara L</creator><creator>Lamsa, Eric</creator><creator>Woods, Michael</creator><creator>Duan, Yin</creator><creator>Fernando, Pasan</creator><creator>Bensimon, Corinne</creator><creator>Kordos, Myra</creator><creator>Guenther, Katharina</creator><creator>Jurek, Paul</creator><creator>Kiefer, Garry E</creator><general>American Chemical Society</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QO</scope><scope>7TM</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>20100317</creationdate><title>Evaluation of Bifunctional Chelates for the Development of Gallium-Based Radiopharmaceuticals</title><author>Ferreira, Cara L ; Lamsa, Eric ; Woods, Michael ; Duan, Yin ; Fernando, Pasan ; Bensimon, Corinne ; Kordos, Myra ; Guenther, Katharina ; Jurek, Paul ; Kiefer, Garry E</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a374t-61a47050251fc146f3cbbc75b1db0ebfc2f6bdd8b32b6d3b631cda32a65d54413</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Animals</topic><topic>Chelating Agents - chemistry</topic><topic>Chelating Agents - pharmacokinetics</topic><topic>Comparative analysis</topic><topic>Gallium Radioisotopes - chemistry</topic><topic>Gallium Radioisotopes - pharmacokinetics</topic><topic>Kidneys</topic><topic>Kinetics</topic><topic>Male</topic><topic>Mice</topic><topic>Mice, Inbred Strains</topic><topic>Molecular Structure</topic><topic>Organometallic Compounds - chemical synthesis</topic><topic>Organometallic Compounds - chemistry</topic><topic>Organometallic Compounds - pharmacokinetics</topic><topic>Positron-Emission Tomography</topic><topic>Radioisotopes</topic><topic>Radiopharmaceuticals - chemical synthesis</topic><topic>Radiopharmaceuticals - chemistry</topic><topic>Radiopharmaceuticals - pharmacokinetics</topic><topic>Rodents</topic><topic>Tissue Distribution</topic><topic>Tissues</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ferreira, Cara L</creatorcontrib><creatorcontrib>Lamsa, Eric</creatorcontrib><creatorcontrib>Woods, Michael</creatorcontrib><creatorcontrib>Duan, Yin</creatorcontrib><creatorcontrib>Fernando, Pasan</creatorcontrib><creatorcontrib>Bensimon, Corinne</creatorcontrib><creatorcontrib>Kordos, Myra</creatorcontrib><creatorcontrib>Guenther, Katharina</creatorcontrib><creatorcontrib>Jurek, Paul</creatorcontrib><creatorcontrib>Kiefer, Garry E</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Bioconjugate chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ferreira, Cara L</au><au>Lamsa, Eric</au><au>Woods, Michael</au><au>Duan, Yin</au><au>Fernando, Pasan</au><au>Bensimon, Corinne</au><au>Kordos, Myra</au><au>Guenther, Katharina</au><au>Jurek, Paul</au><au>Kiefer, Garry E</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Evaluation of Bifunctional Chelates for the Development of Gallium-Based Radiopharmaceuticals</atitle><jtitle>Bioconjugate chemistry</jtitle><addtitle>Bioconjugate Chem</addtitle><date>2010-03-17</date><risdate>2010</risdate><volume>21</volume><issue>3</issue><spage>531</spage><epage>536</epage><pages>531-536</pages><issn>1043-1802</issn><eissn>1520-4812</eissn><abstract>Ga radioisotopes, including the generator-produced positron-emitting isotope 68Ga (t 1/2 = 68 min), are of increasing interest for the development of new radiopharmaceuticals. Bifunctional chelates (BFCs) that can be efficiently radiolabeled with Ga to yield complexes with good in vivo stability are needed. To this end, we undertook a systematic comparison of four BFCs containing different chelating moieties: two novel BFCs, p-NO2-Bn-Oxo (1-oxa-4,7,10-triazacyclododecane-4,7,10-triacetic acid) and p-NO2-Bn-PCTA (3,6,9,15-tetraazabicyclo [9.3.1]pentadeca-1(15),11,13-triene-3,6,9-triacetic acid), and two more commonly used BFCs, p-NO2-Bn-DOTA (1,4,7,10-tetraazacyclododecane-1,4,7,10-tetraacetic acid) and p-NO2-Bn-NOTA (1,4,7-triazacyclononane-1,4,7-triacetic acid). Each BFC was compared with respect to radiolabeling conditions, radiochemical yield, stability, and in vivo clearance properties. p-NO2-Bn-PCTA, p-NO2-Bn-Oxo, and p-NO2-Bn-NOTA were all more efficiently radiolabeled with Ga compared to p-NO2-Bn-DOTA. p-NO2-Bn-DOTA required longer reaction time, higher concentrations of BFC, or heating to obtain equivalent radiochemical yields. Better stability was observed for p-NO2-Bn-NOTA and p-NO2-Bn-PCTA compared to p-NO2-Bn-DOTA and p-NO2-Bn-Oxo, especially with respect to transmetalation to transferrin. Ga-radiolabled p-NO2-Bn-Oxo was found to be kinetically labile and therefore unstable in vivo. Ga-radiolabeled p-NO2-Bn-NOTA and p-NO2-Bn-PCTA were relatively inert, while Ga-radiolabeled p-NO2-Bn-DOTA had intermediate stability, losing >20% of Ga in less than one hour when incubated with apo-transferrin. Similar stability differences were seen when incubating at pH 2. In vivo PET imaging and biodistribution studies in mice showed that 68Ga-radiolabeled p-NO2-Bn-PCTA, p-NO2-Bn-NOTA, and p-NO2-Bn-DOTA all cleared through the kidneys. While there was no statistical difference in the biodistribution results of 68Ga-radiolabeled p-NO2-Bn-PCTA and p-NO2-Bn-DOTA, 68Ga-radiolabeled p-NO2-Bn-NOTA cleared more rapidly from blood and muscle tissue but retained at up to 5 times higher activity in the kidneys.</abstract><cop>United States</cop><pub>American Chemical Society</pub><pmid>20175523</pmid><doi>10.1021/bc900443a</doi><tpages>6</tpages></addata></record> |
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subjects | Animals Chelating Agents - chemistry Chelating Agents - pharmacokinetics Comparative analysis Gallium Radioisotopes - chemistry Gallium Radioisotopes - pharmacokinetics Kidneys Kinetics Male Mice Mice, Inbred Strains Molecular Structure Organometallic Compounds - chemical synthesis Organometallic Compounds - chemistry Organometallic Compounds - pharmacokinetics Positron-Emission Tomography Radioisotopes Radiopharmaceuticals - chemical synthesis Radiopharmaceuticals - chemistry Radiopharmaceuticals - pharmacokinetics Rodents Tissue Distribution Tissues |
title | Evaluation of Bifunctional Chelates for the Development of Gallium-Based Radiopharmaceuticals |
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