99mTcN complexes of tert-butyl dithiocarbamate and methoxyisobutyl dithiocarbamate as myocardial and brain imaging agents

OBJECTIVETwo ligands viz. tert-butyl dithiocarbamate (TBDTC) and methoxyisobutyl dithiocarbamate (MIBDTC), which are analogous to the tert-butyl isonitrile (TBI) and sestamibi (MIBI) ligands, were synthesized and labelled with the [TcN] core to evaluate their potential as myocardial agents. As these...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Nuclear medicine communications 2005-11, Vol.26 (11), p.1013-1019
Hauptverfasser: Mathur, Anupam, Mallia, Madhava B, Subramanian, Suresh, Banerjee, Sharmila, Kothari, K, Dhotare, Bhaskar, Sarma, H.D, Venkatesh, Meera
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 1019
container_issue 11
container_start_page 1013
container_title Nuclear medicine communications
container_volume 26
creator Mathur, Anupam
Mallia, Madhava B
Subramanian, Suresh
Banerjee, Sharmila
Kothari, K
Dhotare, Bhaskar
Sarma, H.D
Venkatesh, Meera
description OBJECTIVETwo ligands viz. tert-butyl dithiocarbamate (TBDTC) and methoxyisobutyl dithiocarbamate (MIBDTC), which are analogous to the tert-butyl isonitrile (TBI) and sestamibi (MIBI) ligands, were synthesized and labelled with the [TcN] core to evaluate their potential as myocardial agents. As these complexes have low molecular weights, and are neutral and lipophilic in nature, they have a tendency to cross the blood–brain barrier and thus deserve evaluation as potential brain perfusion imaging agents. METHODSThe dithiocarbamate ligands were synthesized from their respective amines, i.e., tert-butylamine and methoxyisobutylamine, by reacting with carbon disulfide in dry ether in the presence of crushed sodium hydroxide. The ligands were characterized by elemental analyses. The Tc-nitrido intermediate was prepared from TcO4 using commercially available nitrido kits. The complexation was carried out by mixing the freshly prepared Tc-nitrido intermediate and the ligand followed by incubation at room temperature for 10 min. These complexes were characterized by high-performance liquid chromatography (HPLC) using a C-18 reversed phase column with acetonitrile:water as the mobile phase, and by paper electrophoresis. Biodistribution studies were carried out in normal Swiss mice. RESULTSThe ligands were synthesized in near quantitative yields. They were radiolabelled in > 95% yields using the Tc-nitrido core, at low ligand concentrations of 0.01 mg · ml (5.8×10 M) for TBDTC and 1 mg · ml (4.8×10 M) for MIBDTC, respectively. Both the complexes were found to be neutral and eluted out as single species in HPLC. Both the complexes showed myocardial as well as brain uptake. The TcN(TBDTC)2 complex showed a better heart/blood and heart/lung ratio when compared to TcN(NOEt)2, an agent in phase III clinical trials proposed for myocardial imaging. This complex also showed brain uptake (3.74%ID/g) at 10 min post-injection (p.i.) with brain/blood ratios better than that of the standard agent Tc-D,L-HMPAO at all time points studied. TcN(MIBDTC)2 showed myocardial uptake of 6.41%ID/g at 5 min p.i., which decreased to 1.76%ID/g, 60 min p.i. TcN(MIBDTC)2 also showed good brain uptake (3.21%ID/g at 5 min p.i.) but relatively fast washout (1.33%ID/g at 60 min p.i.) from the target organ. CONCLUSIONBoth the complexes under study showed myocardial as well as brain uptake. The results obtained with TcN(TBDTC)2 shows promise towards its development as a potential brain imaging agent.
doi_str_mv 10.1097/01.mnm.0000183793.51474.2f
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_68663841</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>68663841</sourcerecordid><originalsourceid>FETCH-LOGICAL-c2072-1510a4460cbc6fe2c4062abd72387b5c8131d5a4bf61b27d8f9e185799dbd5963</originalsourceid><addsrcrecordid>eNp1kEtv1TAQRr0A0VL4CyhiwS7BYzu2ww5VFJAq2JS15VfuDdjxxU7U5t_j-5C6Yjajkc43MzoIvQfcAR7ERwxdnGOHa4GkYqBdD0ywjowv0DUGRlvKKb9Cr0v5XRlJuXiFroATLEHia7QNQ3ywPxqb4iH4J1-aNDaLz0tr1mULjZuW_ZSszkZHvfhGz66Jftmnp20q6T9MaeJ2nN2kwylhsp7mZop6N827Ru_8vJQ36OWoQ_FvL_0G_br78nD7rb3_-fX77ef71hIsSAs9YM0Yx9ZYPnpiGeZEGycIlcL0VgIF12tmRg6GCCfHwYPsxTA44_qB0xv04bz3kNPf1ZdFxalYH4KefVqL4pJzKhlU8NMZtDmVkv2oDrm-nDcFWB1lKwyqylbPstVJtiJjDb-7XFlN9O45ejFdAXYGHlOofsufsD76rPZeh2V_WskJhZZg3APUqT0eIfQfwpmQFQ</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>68663841</pqid></control><display><type>article</type><title>99mTcN complexes of tert-butyl dithiocarbamate and methoxyisobutyl dithiocarbamate as myocardial and brain imaging agents</title><source>MEDLINE</source><source>Journals@Ovid Ovid Autoload</source><creator>Mathur, Anupam ; Mallia, Madhava B ; Subramanian, Suresh ; Banerjee, Sharmila ; Kothari, K ; Dhotare, Bhaskar ; Sarma, H.D ; Venkatesh, Meera</creator><creatorcontrib>Mathur, Anupam ; Mallia, Madhava B ; Subramanian, Suresh ; Banerjee, Sharmila ; Kothari, K ; Dhotare, Bhaskar ; Sarma, H.D ; Venkatesh, Meera</creatorcontrib><description>OBJECTIVETwo ligands viz. tert-butyl dithiocarbamate (TBDTC) and methoxyisobutyl dithiocarbamate (MIBDTC), which are analogous to the tert-butyl isonitrile (TBI) and sestamibi (MIBI) ligands, were synthesized and labelled with the [TcN] core to evaluate their potential as myocardial agents. As these complexes have low molecular weights, and are neutral and lipophilic in nature, they have a tendency to cross the blood–brain barrier and thus deserve evaluation as potential brain perfusion imaging agents. METHODSThe dithiocarbamate ligands were synthesized from their respective amines, i.e., tert-butylamine and methoxyisobutylamine, by reacting with carbon disulfide in dry ether in the presence of crushed sodium hydroxide. The ligands were characterized by elemental analyses. The Tc-nitrido intermediate was prepared from TcO4 using commercially available nitrido kits. The complexation was carried out by mixing the freshly prepared Tc-nitrido intermediate and the ligand followed by incubation at room temperature for 10 min. These complexes were characterized by high-performance liquid chromatography (HPLC) using a C-18 reversed phase column with acetonitrile:water as the mobile phase, and by paper electrophoresis. Biodistribution studies were carried out in normal Swiss mice. RESULTSThe ligands were synthesized in near quantitative yields. They were radiolabelled in &gt; 95% yields using the Tc-nitrido core, at low ligand concentrations of 0.01 mg · ml (5.8×10 M) for TBDTC and 1 mg · ml (4.8×10 M) for MIBDTC, respectively. Both the complexes were found to be neutral and eluted out as single species in HPLC. Both the complexes showed myocardial as well as brain uptake. The TcN(TBDTC)2 complex showed a better heart/blood and heart/lung ratio when compared to TcN(NOEt)2, an agent in phase III clinical trials proposed for myocardial imaging. This complex also showed brain uptake (3.74%ID/g) at 10 min post-injection (p.i.) with brain/blood ratios better than that of the standard agent Tc-D,L-HMPAO at all time points studied. TcN(MIBDTC)2 showed myocardial uptake of 6.41%ID/g at 5 min p.i., which decreased to 1.76%ID/g, 60 min p.i. TcN(MIBDTC)2 also showed good brain uptake (3.21%ID/g at 5 min p.i.) but relatively fast washout (1.33%ID/g at 60 min p.i.) from the target organ. CONCLUSIONBoth the complexes under study showed myocardial as well as brain uptake. The results obtained with TcN(TBDTC)2 shows promise towards its development as a potential brain imaging agent.</description><identifier>ISSN: 0143-3636</identifier><identifier>DOI: 10.1097/01.mnm.0000183793.51474.2f</identifier><identifier>PMID: 16208180</identifier><language>eng</language><publisher>England: Lippincott Williams &amp; Wilkins, Inc</publisher><subject>Animals ; Brain - diagnostic imaging ; Brain - metabolism ; Heart - diagnostic imaging ; Metabolic Clearance Rate ; Mice ; Myocardium - metabolism ; Organ Specificity ; Organotechnetium Compounds - pharmacokinetics ; Radionuclide Imaging ; Radiopharmaceuticals - pharmacokinetics ; Tissue Distribution</subject><ispartof>Nuclear medicine communications, 2005-11, Vol.26 (11), p.1013-1019</ispartof><rights>2005 Lippincott Williams &amp; Wilkins, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c2072-1510a4460cbc6fe2c4062abd72387b5c8131d5a4bf61b27d8f9e185799dbd5963</citedby><cites>FETCH-LOGICAL-c2072-1510a4460cbc6fe2c4062abd72387b5c8131d5a4bf61b27d8f9e185799dbd5963</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16208180$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Mathur, Anupam</creatorcontrib><creatorcontrib>Mallia, Madhava B</creatorcontrib><creatorcontrib>Subramanian, Suresh</creatorcontrib><creatorcontrib>Banerjee, Sharmila</creatorcontrib><creatorcontrib>Kothari, K</creatorcontrib><creatorcontrib>Dhotare, Bhaskar</creatorcontrib><creatorcontrib>Sarma, H.D</creatorcontrib><creatorcontrib>Venkatesh, Meera</creatorcontrib><title>99mTcN complexes of tert-butyl dithiocarbamate and methoxyisobutyl dithiocarbamate as myocardial and brain imaging agents</title><title>Nuclear medicine communications</title><addtitle>Nucl Med Commun</addtitle><description>OBJECTIVETwo ligands viz. tert-butyl dithiocarbamate (TBDTC) and methoxyisobutyl dithiocarbamate (MIBDTC), which are analogous to the tert-butyl isonitrile (TBI) and sestamibi (MIBI) ligands, were synthesized and labelled with the [TcN] core to evaluate their potential as myocardial agents. As these complexes have low molecular weights, and are neutral and lipophilic in nature, they have a tendency to cross the blood–brain barrier and thus deserve evaluation as potential brain perfusion imaging agents. METHODSThe dithiocarbamate ligands were synthesized from their respective amines, i.e., tert-butylamine and methoxyisobutylamine, by reacting with carbon disulfide in dry ether in the presence of crushed sodium hydroxide. The ligands were characterized by elemental analyses. The Tc-nitrido intermediate was prepared from TcO4 using commercially available nitrido kits. The complexation was carried out by mixing the freshly prepared Tc-nitrido intermediate and the ligand followed by incubation at room temperature for 10 min. These complexes were characterized by high-performance liquid chromatography (HPLC) using a C-18 reversed phase column with acetonitrile:water as the mobile phase, and by paper electrophoresis. Biodistribution studies were carried out in normal Swiss mice. RESULTSThe ligands were synthesized in near quantitative yields. They were radiolabelled in &gt; 95% yields using the Tc-nitrido core, at low ligand concentrations of 0.01 mg · ml (5.8×10 M) for TBDTC and 1 mg · ml (4.8×10 M) for MIBDTC, respectively. Both the complexes were found to be neutral and eluted out as single species in HPLC. Both the complexes showed myocardial as well as brain uptake. The TcN(TBDTC)2 complex showed a better heart/blood and heart/lung ratio when compared to TcN(NOEt)2, an agent in phase III clinical trials proposed for myocardial imaging. This complex also showed brain uptake (3.74%ID/g) at 10 min post-injection (p.i.) with brain/blood ratios better than that of the standard agent Tc-D,L-HMPAO at all time points studied. TcN(MIBDTC)2 showed myocardial uptake of 6.41%ID/g at 5 min p.i., which decreased to 1.76%ID/g, 60 min p.i. TcN(MIBDTC)2 also showed good brain uptake (3.21%ID/g at 5 min p.i.) but relatively fast washout (1.33%ID/g at 60 min p.i.) from the target organ. CONCLUSIONBoth the complexes under study showed myocardial as well as brain uptake. The results obtained with TcN(TBDTC)2 shows promise towards its development as a potential brain imaging agent.</description><subject>Animals</subject><subject>Brain - diagnostic imaging</subject><subject>Brain - metabolism</subject><subject>Heart - diagnostic imaging</subject><subject>Metabolic Clearance Rate</subject><subject>Mice</subject><subject>Myocardium - metabolism</subject><subject>Organ Specificity</subject><subject>Organotechnetium Compounds - pharmacokinetics</subject><subject>Radionuclide Imaging</subject><subject>Radiopharmaceuticals - pharmacokinetics</subject><subject>Tissue Distribution</subject><issn>0143-3636</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kEtv1TAQRr0A0VL4CyhiwS7BYzu2ww5VFJAq2JS15VfuDdjxxU7U5t_j-5C6Yjajkc43MzoIvQfcAR7ERwxdnGOHa4GkYqBdD0ywjowv0DUGRlvKKb9Cr0v5XRlJuXiFroATLEHia7QNQ3ywPxqb4iH4J1-aNDaLz0tr1mULjZuW_ZSszkZHvfhGz66Jftmnp20q6T9MaeJ2nN2kwylhsp7mZop6N827Ru_8vJQ36OWoQ_FvL_0G_br78nD7rb3_-fX77ef71hIsSAs9YM0Yx9ZYPnpiGeZEGycIlcL0VgIF12tmRg6GCCfHwYPsxTA44_qB0xv04bz3kNPf1ZdFxalYH4KefVqL4pJzKhlU8NMZtDmVkv2oDrm-nDcFWB1lKwyqylbPstVJtiJjDb-7XFlN9O45ejFdAXYGHlOofsufsD76rPZeh2V_WskJhZZg3APUqT0eIfQfwpmQFQ</recordid><startdate>200511</startdate><enddate>200511</enddate><creator>Mathur, Anupam</creator><creator>Mallia, Madhava B</creator><creator>Subramanian, Suresh</creator><creator>Banerjee, Sharmila</creator><creator>Kothari, K</creator><creator>Dhotare, Bhaskar</creator><creator>Sarma, H.D</creator><creator>Venkatesh, Meera</creator><general>Lippincott Williams &amp; Wilkins, Inc</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>7X8</scope></search><sort><creationdate>200511</creationdate><title>99mTcN complexes of tert-butyl dithiocarbamate and methoxyisobutyl dithiocarbamate as myocardial and brain imaging agents</title><author>Mathur, Anupam ; Mallia, Madhava B ; Subramanian, Suresh ; Banerjee, Sharmila ; Kothari, K ; Dhotare, Bhaskar ; Sarma, H.D ; Venkatesh, Meera</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2072-1510a4460cbc6fe2c4062abd72387b5c8131d5a4bf61b27d8f9e185799dbd5963</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Animals</topic><topic>Brain - diagnostic imaging</topic><topic>Brain - metabolism</topic><topic>Heart - diagnostic imaging</topic><topic>Metabolic Clearance Rate</topic><topic>Mice</topic><topic>Myocardium - metabolism</topic><topic>Organ Specificity</topic><topic>Organotechnetium Compounds - pharmacokinetics</topic><topic>Radionuclide Imaging</topic><topic>Radiopharmaceuticals - pharmacokinetics</topic><topic>Tissue Distribution</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mathur, Anupam</creatorcontrib><creatorcontrib>Mallia, Madhava B</creatorcontrib><creatorcontrib>Subramanian, Suresh</creatorcontrib><creatorcontrib>Banerjee, Sharmila</creatorcontrib><creatorcontrib>Kothari, K</creatorcontrib><creatorcontrib>Dhotare, Bhaskar</creatorcontrib><creatorcontrib>Sarma, H.D</creatorcontrib><creatorcontrib>Venkatesh, Meera</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Nuclear medicine communications</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mathur, Anupam</au><au>Mallia, Madhava B</au><au>Subramanian, Suresh</au><au>Banerjee, Sharmila</au><au>Kothari, K</au><au>Dhotare, Bhaskar</au><au>Sarma, H.D</au><au>Venkatesh, Meera</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>99mTcN complexes of tert-butyl dithiocarbamate and methoxyisobutyl dithiocarbamate as myocardial and brain imaging agents</atitle><jtitle>Nuclear medicine communications</jtitle><addtitle>Nucl Med Commun</addtitle><date>2005-11</date><risdate>2005</risdate><volume>26</volume><issue>11</issue><spage>1013</spage><epage>1019</epage><pages>1013-1019</pages><issn>0143-3636</issn><abstract>OBJECTIVETwo ligands viz. tert-butyl dithiocarbamate (TBDTC) and methoxyisobutyl dithiocarbamate (MIBDTC), which are analogous to the tert-butyl isonitrile (TBI) and sestamibi (MIBI) ligands, were synthesized and labelled with the [TcN] core to evaluate their potential as myocardial agents. As these complexes have low molecular weights, and are neutral and lipophilic in nature, they have a tendency to cross the blood–brain barrier and thus deserve evaluation as potential brain perfusion imaging agents. METHODSThe dithiocarbamate ligands were synthesized from their respective amines, i.e., tert-butylamine and methoxyisobutylamine, by reacting with carbon disulfide in dry ether in the presence of crushed sodium hydroxide. The ligands were characterized by elemental analyses. The Tc-nitrido intermediate was prepared from TcO4 using commercially available nitrido kits. The complexation was carried out by mixing the freshly prepared Tc-nitrido intermediate and the ligand followed by incubation at room temperature for 10 min. These complexes were characterized by high-performance liquid chromatography (HPLC) using a C-18 reversed phase column with acetonitrile:water as the mobile phase, and by paper electrophoresis. Biodistribution studies were carried out in normal Swiss mice. RESULTSThe ligands were synthesized in near quantitative yields. They were radiolabelled in &gt; 95% yields using the Tc-nitrido core, at low ligand concentrations of 0.01 mg · ml (5.8×10 M) for TBDTC and 1 mg · ml (4.8×10 M) for MIBDTC, respectively. Both the complexes were found to be neutral and eluted out as single species in HPLC. Both the complexes showed myocardial as well as brain uptake. The TcN(TBDTC)2 complex showed a better heart/blood and heart/lung ratio when compared to TcN(NOEt)2, an agent in phase III clinical trials proposed for myocardial imaging. This complex also showed brain uptake (3.74%ID/g) at 10 min post-injection (p.i.) with brain/blood ratios better than that of the standard agent Tc-D,L-HMPAO at all time points studied. TcN(MIBDTC)2 showed myocardial uptake of 6.41%ID/g at 5 min p.i., which decreased to 1.76%ID/g, 60 min p.i. TcN(MIBDTC)2 also showed good brain uptake (3.21%ID/g at 5 min p.i.) but relatively fast washout (1.33%ID/g at 60 min p.i.) from the target organ. CONCLUSIONBoth the complexes under study showed myocardial as well as brain uptake. The results obtained with TcN(TBDTC)2 shows promise towards its development as a potential brain imaging agent.</abstract><cop>England</cop><pub>Lippincott Williams &amp; Wilkins, Inc</pub><pmid>16208180</pmid><doi>10.1097/01.mnm.0000183793.51474.2f</doi><tpages>7</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0143-3636
ispartof Nuclear medicine communications, 2005-11, Vol.26 (11), p.1013-1019
issn 0143-3636
language eng
recordid cdi_proquest_miscellaneous_68663841
source MEDLINE; Journals@Ovid Ovid Autoload
subjects Animals
Brain - diagnostic imaging
Brain - metabolism
Heart - diagnostic imaging
Metabolic Clearance Rate
Mice
Myocardium - metabolism
Organ Specificity
Organotechnetium Compounds - pharmacokinetics
Radionuclide Imaging
Radiopharmaceuticals - pharmacokinetics
Tissue Distribution
title 99mTcN complexes of tert-butyl dithiocarbamate and methoxyisobutyl dithiocarbamate as myocardial and brain imaging agents
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-25T07%3A42%3A20IST&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=99mTcN%20complexes%20of%20tert-butyl%20dithiocarbamate%20and%20methoxyisobutyl%20dithiocarbamate%20as%20myocardial%20and%20brain%20imaging%20agents&rft.jtitle=Nuclear%20medicine%20communications&rft.au=Mathur,%20Anupam&rft.date=2005-11&rft.volume=26&rft.issue=11&rft.spage=1013&rft.epage=1019&rft.pages=1013-1019&rft.issn=0143-3636&rft_id=info:doi/10.1097/01.mnm.0000183793.51474.2f&rft_dat=%3Cproquest_cross%3E68663841%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=68663841&rft_id=info:pmid/16208180&rfr_iscdi=true