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...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Bioconjugate chemistry 2010-03, Vol.21 (3), p.531-536
Hauptverfasser: Ferreira, Cara L, Lamsa, Eric, Woods, Michael, Duan, Yin, Fernando, Pasan, Bensimon, Corinne, Kordos, Myra, Guenther, Katharina, Jurek, Paul, Kiefer, Garry E
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 536
container_issue 3
container_start_page 531
container_title Bioconjugate chemistry
container_volume 21
creator Ferreira, Cara L
Lamsa, Eric
Woods, Michael
Duan, Yin
Fernando, Pasan
Bensimon, Corinne
Kordos, Myra
Guenther, Katharina
Jurek, Paul
Kiefer, Garry E
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
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_754547342</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>754547342</sourcerecordid><originalsourceid>FETCH-LOGICAL-a374t-61a47050251fc146f3cbbc75b1db0ebfc2f6bdd8b32b6d3b631cda32a65d54413</originalsourceid><addsrcrecordid>eNp90dtKw0AQBuBFFK3VC19AgiDqRXRnD0lzaesRCoLopYTZE41sujWbFHx7U-oBFLyaHfj4F-Yn5ADoOVAGF0oXlArBcYMMQDKaihGwzf5NBU9hRNkO2Y3xlVJawIhtkx1GIZeS8QF5uV6i77CtwjwJLhlXrpvr1YY-mcysx9bGxIUmaWc2ubJL68OitvN2hW_R-6qr0zFGa5JHNFVYzLCpUduurTT6uEe2XD_s_ucckueb66fJXTp9uL2fXE5T5Llo0wxQ5FRSJsFpEJnjWimdSwVGUaucZi5TxowUZyozXGUctEHOMJNGCgF8SE7WuYsmvHU2tmVdRW29x7kNXSxzKaTIuWC9PP1XgigKYEUueE-PftHX0DX9YWLJIIOCglyhszXSTYixsa5cNFWNzXsJtFyVU36X09vDz8BO1dZ8y682enC8Bqjjz2d_gz4APxOVGg</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>216190153</pqid></control><display><type>article</type><title>Evaluation of Bifunctional Chelates for the Development of Gallium-Based Radiopharmaceuticals</title><source>MEDLINE</source><source>American Chemical Society Journals</source><creator>Ferreira, Cara L ; Lamsa, Eric ; Woods, Michael ; Duan, Yin ; Fernando, Pasan ; Bensimon, Corinne ; Kordos, Myra ; Guenther, Katharina ; Jurek, Paul ; Kiefer, Garry E</creator><creatorcontrib>Ferreira, Cara L ; Lamsa, Eric ; Woods, Michael ; Duan, Yin ; Fernando, Pasan ; Bensimon, Corinne ; Kordos, Myra ; Guenther, Katharina ; Jurek, Paul ; Kiefer, Garry E</creatorcontrib><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 &gt;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 &gt;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 &gt;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>
fulltext fulltext
identifier ISSN: 1043-1802
ispartof Bioconjugate chemistry, 2010-03, Vol.21 (3), p.531-536
issn 1043-1802
1520-4812
language eng
recordid cdi_proquest_miscellaneous_754547342
source MEDLINE; American Chemical Society Journals
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
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-10T07%3A26%3A15IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Evaluation%20of%20Bifunctional%20Chelates%20for%20the%20Development%20of%20Gallium-Based%20Radiopharmaceuticals&rft.jtitle=Bioconjugate%20chemistry&rft.au=Ferreira,%20Cara%20L&rft.date=2010-03-17&rft.volume=21&rft.issue=3&rft.spage=531&rft.epage=536&rft.pages=531-536&rft.issn=1043-1802&rft.eissn=1520-4812&rft_id=info:doi/10.1021/bc900443a&rft_dat=%3Cproquest_cross%3E754547342%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=216190153&rft_id=info:pmid/20175523&rfr_iscdi=true