Silicon compounds in carbon-11 radiochemistry: present use and future perspectives
Positron emission tomography (PET) is a powerful functional imaging technique that requires the use of positron emitting nuclides. Carbon-11 ( 11 C) radionuclide has several advantages related to the ubiquity of carbon atoms in biomolecules and the conservation of pharmacological properties of the m...
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Veröffentlicht in: | Organic & biomolecular chemistry 2021-08, Vol.19 (32), p.6916-6925 |
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description | Positron emission tomography (PET) is a powerful functional imaging technique that requires the use of positron emitting nuclides. Carbon-11 (
11
C) radionuclide has several advantages related to the ubiquity of carbon atoms in biomolecules and the conservation of pharmacological properties of the molecule upon isotopic exchange of carbon-12 with carbon-11. However, due to the short half-life of
11
C (20.4 minutes) and the low scale with which it is produced by the cyclotron (sub-nanomolar concentrations), quick, robust and chemospecific radiolabelling strategies are required to minimise activity loss during incorporation of the
11
C nuclide into the final product. To address some of the constraints of working with
11
C, the use of silicon-based chemistry for
11
C-labelling was proposed as a rapid and effective route for radiopharmaceutical production due to the broad applicability and high efficiency showed in organic chemistry. In the past years several organic chemistry methodologies have been successfully applied to
11
C-chemistry. In this short review, we examine silicon-based
11
C-chemistry, with a particular emphasis on the radiotracers that have been successfully produced and potential improvements to further expand the applicability of silicon in radiochemistry.
The use of silicon-based reagents and precursors for carbon-11 labelling has shown wide applicability and robustness with short reaction times using mild conditions. In this review, recent advances and future perspectives are examined. |
doi_str_mv | 10.1039/d1ob01202a |
format | Article |
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11
C) radionuclide has several advantages related to the ubiquity of carbon atoms in biomolecules and the conservation of pharmacological properties of the molecule upon isotopic exchange of carbon-12 with carbon-11. However, due to the short half-life of
11
C (20.4 minutes) and the low scale with which it is produced by the cyclotron (sub-nanomolar concentrations), quick, robust and chemospecific radiolabelling strategies are required to minimise activity loss during incorporation of the
11
C nuclide into the final product. To address some of the constraints of working with
11
C, the use of silicon-based chemistry for
11
C-labelling was proposed as a rapid and effective route for radiopharmaceutical production due to the broad applicability and high efficiency showed in organic chemistry. In the past years several organic chemistry methodologies have been successfully applied to
11
C-chemistry. In this short review, we examine silicon-based
11
C-chemistry, with a particular emphasis on the radiotracers that have been successfully produced and potential improvements to further expand the applicability of silicon in radiochemistry.
The use of silicon-based reagents and precursors for carbon-11 labelling has shown wide applicability and robustness with short reaction times using mild conditions. In this review, recent advances and future perspectives are examined.</description><identifier>ISSN: 1477-0520</identifier><identifier>EISSN: 1477-0539</identifier><identifier>DOI: 10.1039/d1ob01202a</identifier><identifier>PMID: 34319335</identifier><language>eng</language><publisher>England: Royal Society of Chemistry</publisher><subject>Biomolecules ; Carbon ; Carbon 12 ; Chemistry ; Cyclotrons ; Imaging techniques ; Labeling ; Nuclides ; Organic chemistry ; Pharmaceuticals ; Positron emission ; Positron emission tomography ; Radioactive tracers ; Radiochemistry ; Radioisotopes ; Radiolabelling ; Silicon ; Silicon compounds ; Tomography</subject><ispartof>Organic & biomolecular chemistry, 2021-08, Vol.19 (32), p.6916-6925</ispartof><rights>Copyright Royal Society of Chemistry 2021</rights><rights>This journal is © The Royal Society of Chemistry 2021 The Royal Society of Chemistry</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c428t-f239cbf1ab1f0f384131ebef0280068bf41b97e099809ab375d29c3bb20cd8e93</citedby><cites>FETCH-LOGICAL-c428t-f239cbf1ab1f0f384131ebef0280068bf41b97e099809ab375d29c3bb20cd8e93</cites><orcidid>0000-0001-8389-9012 ; 0000-0001-8993-2717 ; 0000-0002-1309-3045</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,778,782,883,27907,27908</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34319335$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Luzi, Federico</creatorcontrib><creatorcontrib>Gee, Antony D</creatorcontrib><creatorcontrib>Bongarzone, Salvatore</creatorcontrib><title>Silicon compounds in carbon-11 radiochemistry: present use and future perspectives</title><title>Organic & biomolecular chemistry</title><addtitle>Org Biomol Chem</addtitle><description>Positron emission tomography (PET) is a powerful functional imaging technique that requires the use of positron emitting nuclides. Carbon-11 (
11
C) radionuclide has several advantages related to the ubiquity of carbon atoms in biomolecules and the conservation of pharmacological properties of the molecule upon isotopic exchange of carbon-12 with carbon-11. However, due to the short half-life of
11
C (20.4 minutes) and the low scale with which it is produced by the cyclotron (sub-nanomolar concentrations), quick, robust and chemospecific radiolabelling strategies are required to minimise activity loss during incorporation of the
11
C nuclide into the final product. To address some of the constraints of working with
11
C, the use of silicon-based chemistry for
11
C-labelling was proposed as a rapid and effective route for radiopharmaceutical production due to the broad applicability and high efficiency showed in organic chemistry. In the past years several organic chemistry methodologies have been successfully applied to
11
C-chemistry. In this short review, we examine silicon-based
11
C-chemistry, with a particular emphasis on the radiotracers that have been successfully produced and potential improvements to further expand the applicability of silicon in radiochemistry.
The use of silicon-based reagents and precursors for carbon-11 labelling has shown wide applicability and robustness with short reaction times using mild conditions. In this review, recent advances and future perspectives are examined.</description><subject>Biomolecules</subject><subject>Carbon</subject><subject>Carbon 12</subject><subject>Chemistry</subject><subject>Cyclotrons</subject><subject>Imaging techniques</subject><subject>Labeling</subject><subject>Nuclides</subject><subject>Organic chemistry</subject><subject>Pharmaceuticals</subject><subject>Positron emission</subject><subject>Positron emission tomography</subject><subject>Radioactive tracers</subject><subject>Radiochemistry</subject><subject>Radioisotopes</subject><subject>Radiolabelling</subject><subject>Silicon</subject><subject>Silicon compounds</subject><subject>Tomography</subject><issn>1477-0520</issn><issn>1477-0539</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNpdkUuLFTEQhYMozkM37pUGNyK0ViXp24kLYRyfMDDgYx2SdMXJ0LfTJt0D8-8nesfrY1VV1MfhHA5jjxBeIAj9csDkADlwe4cdouz7Fjqh7-53DgfsqJRLANT9Rt5nB0IK1EJ0h-zzlzhGn6bGp-2c1mkoTayHzS5NLWKT7RCTv6BtLEu-ftXMmQpNS7MWauw0NGFd1kzNTLnM5Jd4ReUBuxfsWOjh7Txm396_-3r6sT07__Dp9OSs9ZKrpQ1caO8CWocBglASBZKjAFwBbJQLEp3uCbRWoK0TfTdw7YVzHPygSItj9nqnO69uS4OvtrIdzZzj1uZrk2w0_36meGG-pyujRM8l9lXg2a1ATj9WKoupKT2No50orcXwrut0z5USFX36H3qZ1jzVeJXacC5Ayk2lnu8on1MpmcLeDIL5WZV5i-dvflV1UuEnf9vfo7-7qcDjHZCL33__dC1uAKq3mVU</recordid><startdate>20210828</startdate><enddate>20210828</enddate><creator>Luzi, Federico</creator><creator>Gee, Antony D</creator><creator>Bongarzone, Salvatore</creator><general>Royal Society of Chemistry</general><general>The Royal Society of Chemistry</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QO</scope><scope>7T7</scope><scope>7TM</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>P64</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0001-8389-9012</orcidid><orcidid>https://orcid.org/0000-0001-8993-2717</orcidid><orcidid>https://orcid.org/0000-0002-1309-3045</orcidid></search><sort><creationdate>20210828</creationdate><title>Silicon compounds in carbon-11 radiochemistry: present use and future perspectives</title><author>Luzi, Federico ; Gee, Antony D ; Bongarzone, Salvatore</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c428t-f239cbf1ab1f0f384131ebef0280068bf41b97e099809ab375d29c3bb20cd8e93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Biomolecules</topic><topic>Carbon</topic><topic>Carbon 12</topic><topic>Chemistry</topic><topic>Cyclotrons</topic><topic>Imaging techniques</topic><topic>Labeling</topic><topic>Nuclides</topic><topic>Organic chemistry</topic><topic>Pharmaceuticals</topic><topic>Positron emission</topic><topic>Positron emission tomography</topic><topic>Radioactive tracers</topic><topic>Radiochemistry</topic><topic>Radioisotopes</topic><topic>Radiolabelling</topic><topic>Silicon</topic><topic>Silicon compounds</topic><topic>Tomography</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Luzi, Federico</creatorcontrib><creatorcontrib>Gee, Antony D</creatorcontrib><creatorcontrib>Bongarzone, Salvatore</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Nucleic Acids Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Organic & biomolecular chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Luzi, Federico</au><au>Gee, Antony D</au><au>Bongarzone, Salvatore</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Silicon compounds in carbon-11 radiochemistry: present use and future perspectives</atitle><jtitle>Organic & biomolecular chemistry</jtitle><addtitle>Org Biomol Chem</addtitle><date>2021-08-28</date><risdate>2021</risdate><volume>19</volume><issue>32</issue><spage>6916</spage><epage>6925</epage><pages>6916-6925</pages><issn>1477-0520</issn><eissn>1477-0539</eissn><abstract>Positron emission tomography (PET) is a powerful functional imaging technique that requires the use of positron emitting nuclides. Carbon-11 (
11
C) radionuclide has several advantages related to the ubiquity of carbon atoms in biomolecules and the conservation of pharmacological properties of the molecule upon isotopic exchange of carbon-12 with carbon-11. However, due to the short half-life of
11
C (20.4 minutes) and the low scale with which it is produced by the cyclotron (sub-nanomolar concentrations), quick, robust and chemospecific radiolabelling strategies are required to minimise activity loss during incorporation of the
11
C nuclide into the final product. To address some of the constraints of working with
11
C, the use of silicon-based chemistry for
11
C-labelling was proposed as a rapid and effective route for radiopharmaceutical production due to the broad applicability and high efficiency showed in organic chemistry. In the past years several organic chemistry methodologies have been successfully applied to
11
C-chemistry. In this short review, we examine silicon-based
11
C-chemistry, with a particular emphasis on the radiotracers that have been successfully produced and potential improvements to further expand the applicability of silicon in radiochemistry.
The use of silicon-based reagents and precursors for carbon-11 labelling has shown wide applicability and robustness with short reaction times using mild conditions. In this review, recent advances and future perspectives are examined.</abstract><cop>England</cop><pub>Royal Society of Chemistry</pub><pmid>34319335</pmid><doi>10.1039/d1ob01202a</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0001-8389-9012</orcidid><orcidid>https://orcid.org/0000-0001-8993-2717</orcidid><orcidid>https://orcid.org/0000-0002-1309-3045</orcidid><oa>free_for_read</oa></addata></record> |
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source | Royal Society Of Chemistry Journals 2008-; Alma/SFX Local Collection |
subjects | Biomolecules Carbon Carbon 12 Chemistry Cyclotrons Imaging techniques Labeling Nuclides Organic chemistry Pharmaceuticals Positron emission Positron emission tomography Radioactive tracers Radiochemistry Radioisotopes Radiolabelling Silicon Silicon compounds Tomography |
title | Silicon compounds in carbon-11 radiochemistry: present use and future perspectives |
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