Synthesis and primary biological evaluation of ReN-NEMPTDD

A new nitrido-Re complex, ReN-NEMPTDD, was synthesized through a modified method in high yield. This complex was stable in vitro. The biodistribution in normal mice showed that this ReN complex accumulated in the liver and was eliminated quickly from almost all organs. VX2 carcinoma was grown in the...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Journal of radioanalytical and nuclear chemistry 2008-08, Vol.277 (2), p.365-369
Hauptverfasser: Wang, Guan-Quan, Zhang, Ji, Luo, Shun-Zhong, Wang, Na, Wei, Hong-Yuan, Wang, Wen-Jin, Yang, Yu-Qing, Liu, Guo-Ping, Yu, Xiao-Qi
Format: Artikel
Sprache:eng
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 369
container_issue 2
container_start_page 365
container_title Journal of radioanalytical and nuclear chemistry
container_volume 277
creator Wang, Guan-Quan
Zhang, Ji
Luo, Shun-Zhong
Wang, Na
Wei, Hong-Yuan
Wang, Wen-Jin
Yang, Yu-Qing
Liu, Guo-Ping
Yu, Xiao-Qi
description A new nitrido-Re complex, ReN-NEMPTDD, was synthesized through a modified method in high yield. This complex was stable in vitro. The biodistribution in normal mice showed that this ReN complex accumulated in the liver and was eliminated quickly from almost all organs. VX2 carcinoma was grown in the livers of rabbits. Transcatheter arterial embolization (TAE) was performed using ReN-NEMPTDD/lipiodol solution. The SPECT images showed that the lipiodol solution could be concentrated in the tumor for about 12 hours. These results indicated that ReN-NEMPTDD/lipiodol could be a potential radiopharmaceutical for liver cancer.
doi_str_mv 10.1007/s10967-007-7033-2
format Article
fullrecord <record><control><sourceid>proquest</sourceid><recordid>TN_cdi_proquest_miscellaneous_34049639</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>34049639</sourcerecordid><originalsourceid>FETCH-LOGICAL-p101t-1a9a91280f39238bd9f3a5e2f8ed874c8285c0031d60d4c6bff3915d38aa43573</originalsourceid><addsrcrecordid>eNotjjtPwzAURj2ARCn8ADZPbIZr3zxsNtSWh1QKgjJXN7ENRmkc4gSp_55IMH1nODr6GLuQcCUByuskwRSlmFCUgCjUEZuBwkLkJcoTdprSFwAYrXHGbt4O7fDpUkicWsu7PuypP_AqxCZ-hJoa7n6oGWkIseXR81e3EZvV08t2uTxjx56a5M7_d87e71bbxYNYP98_Lm7XopMgByHJkJFKg0ejUFfWeKTcKa-d1WVWa6XzGgClLcBmdVH5SZS5RU2U4XR5zi7_ul0fv0eXht0-pNo1DbUujmmHGWSmQIO_phhH8A</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>34049639</pqid></control><display><type>article</type><title>Synthesis and primary biological evaluation of ReN-NEMPTDD</title><source>SpringerLink Journals - AutoHoldings</source><creator>Wang, Guan-Quan ; Zhang, Ji ; Luo, Shun-Zhong ; Wang, Na ; Wei, Hong-Yuan ; Wang, Wen-Jin ; Yang, Yu-Qing ; Liu, Guo-Ping ; Yu, Xiao-Qi</creator><creatorcontrib>Wang, Guan-Quan ; Zhang, Ji ; Luo, Shun-Zhong ; Wang, Na ; Wei, Hong-Yuan ; Wang, Wen-Jin ; Yang, Yu-Qing ; Liu, Guo-Ping ; Yu, Xiao-Qi</creatorcontrib><description>A new nitrido-Re complex, ReN-NEMPTDD, was synthesized through a modified method in high yield. This complex was stable in vitro. The biodistribution in normal mice showed that this ReN complex accumulated in the liver and was eliminated quickly from almost all organs. VX2 carcinoma was grown in the livers of rabbits. Transcatheter arterial embolization (TAE) was performed using ReN-NEMPTDD/lipiodol solution. The SPECT images showed that the lipiodol solution could be concentrated in the tumor for about 12 hours. These results indicated that ReN-NEMPTDD/lipiodol could be a potential radiopharmaceutical for liver cancer.</description><identifier>ISSN: 0236-5731</identifier><identifier>DOI: 10.1007/s10967-007-7033-2</identifier><language>eng</language><ispartof>Journal of radioanalytical and nuclear chemistry, 2008-08, Vol.277 (2), p.365-369</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids></links><search><creatorcontrib>Wang, Guan-Quan</creatorcontrib><creatorcontrib>Zhang, Ji</creatorcontrib><creatorcontrib>Luo, Shun-Zhong</creatorcontrib><creatorcontrib>Wang, Na</creatorcontrib><creatorcontrib>Wei, Hong-Yuan</creatorcontrib><creatorcontrib>Wang, Wen-Jin</creatorcontrib><creatorcontrib>Yang, Yu-Qing</creatorcontrib><creatorcontrib>Liu, Guo-Ping</creatorcontrib><creatorcontrib>Yu, Xiao-Qi</creatorcontrib><title>Synthesis and primary biological evaluation of ReN-NEMPTDD</title><title>Journal of radioanalytical and nuclear chemistry</title><description>A new nitrido-Re complex, ReN-NEMPTDD, was synthesized through a modified method in high yield. This complex was stable in vitro. The biodistribution in normal mice showed that this ReN complex accumulated in the liver and was eliminated quickly from almost all organs. VX2 carcinoma was grown in the livers of rabbits. Transcatheter arterial embolization (TAE) was performed using ReN-NEMPTDD/lipiodol solution. The SPECT images showed that the lipiodol solution could be concentrated in the tumor for about 12 hours. These results indicated that ReN-NEMPTDD/lipiodol could be a potential radiopharmaceutical for liver cancer.</description><issn>0236-5731</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><recordid>eNotjjtPwzAURj2ARCn8ADZPbIZr3zxsNtSWh1QKgjJXN7ENRmkc4gSp_55IMH1nODr6GLuQcCUByuskwRSlmFCUgCjUEZuBwkLkJcoTdprSFwAYrXHGbt4O7fDpUkicWsu7PuypP_AqxCZ-hJoa7n6oGWkIseXR81e3EZvV08t2uTxjx56a5M7_d87e71bbxYNYP98_Lm7XopMgByHJkJFKg0ejUFfWeKTcKa-d1WVWa6XzGgClLcBmdVH5SZS5RU2U4XR5zi7_ul0fv0eXht0-pNo1DbUujmmHGWSmQIO_phhH8A</recordid><startdate>20080801</startdate><enddate>20080801</enddate><creator>Wang, Guan-Quan</creator><creator>Zhang, Ji</creator><creator>Luo, Shun-Zhong</creator><creator>Wang, Na</creator><creator>Wei, Hong-Yuan</creator><creator>Wang, Wen-Jin</creator><creator>Yang, Yu-Qing</creator><creator>Liu, Guo-Ping</creator><creator>Yu, Xiao-Qi</creator><scope>7SR</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope><scope>L7M</scope></search><sort><creationdate>20080801</creationdate><title>Synthesis and primary biological evaluation of ReN-NEMPTDD</title><author>Wang, Guan-Quan ; Zhang, Ji ; Luo, Shun-Zhong ; Wang, Na ; Wei, Hong-Yuan ; Wang, Wen-Jin ; Yang, Yu-Qing ; Liu, Guo-Ping ; Yu, Xiao-Qi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p101t-1a9a91280f39238bd9f3a5e2f8ed874c8285c0031d60d4c6bff3915d38aa43573</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wang, Guan-Quan</creatorcontrib><creatorcontrib>Zhang, Ji</creatorcontrib><creatorcontrib>Luo, Shun-Zhong</creatorcontrib><creatorcontrib>Wang, Na</creatorcontrib><creatorcontrib>Wei, Hong-Yuan</creatorcontrib><creatorcontrib>Wang, Wen-Jin</creatorcontrib><creatorcontrib>Yang, Yu-Qing</creatorcontrib><creatorcontrib>Liu, Guo-Ping</creatorcontrib><creatorcontrib>Yu, Xiao-Qi</creatorcontrib><collection>Engineered Materials Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><jtitle>Journal of radioanalytical and nuclear chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wang, Guan-Quan</au><au>Zhang, Ji</au><au>Luo, Shun-Zhong</au><au>Wang, Na</au><au>Wei, Hong-Yuan</au><au>Wang, Wen-Jin</au><au>Yang, Yu-Qing</au><au>Liu, Guo-Ping</au><au>Yu, Xiao-Qi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synthesis and primary biological evaluation of ReN-NEMPTDD</atitle><jtitle>Journal of radioanalytical and nuclear chemistry</jtitle><date>2008-08-01</date><risdate>2008</risdate><volume>277</volume><issue>2</issue><spage>365</spage><epage>369</epage><pages>365-369</pages><issn>0236-5731</issn><abstract>A new nitrido-Re complex, ReN-NEMPTDD, was synthesized through a modified method in high yield. This complex was stable in vitro. The biodistribution in normal mice showed that this ReN complex accumulated in the liver and was eliminated quickly from almost all organs. VX2 carcinoma was grown in the livers of rabbits. Transcatheter arterial embolization (TAE) was performed using ReN-NEMPTDD/lipiodol solution. The SPECT images showed that the lipiodol solution could be concentrated in the tumor for about 12 hours. These results indicated that ReN-NEMPTDD/lipiodol could be a potential radiopharmaceutical for liver cancer.</abstract><doi>10.1007/s10967-007-7033-2</doi><tpages>5</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0236-5731
ispartof Journal of radioanalytical and nuclear chemistry, 2008-08, Vol.277 (2), p.365-369
issn 0236-5731
language eng
recordid cdi_proquest_miscellaneous_34049639
source SpringerLink Journals - AutoHoldings
title Synthesis and primary biological evaluation of ReN-NEMPTDD
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-03T16%3A21%3A12IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Synthesis%20and%20primary%20biological%20evaluation%20of%20ReN-NEMPTDD&rft.jtitle=Journal%20of%20radioanalytical%20and%20nuclear%20chemistry&rft.au=Wang,%20Guan-Quan&rft.date=2008-08-01&rft.volume=277&rft.issue=2&rft.spage=365&rft.epage=369&rft.pages=365-369&rft.issn=0236-5731&rft_id=info:doi/10.1007/s10967-007-7033-2&rft_dat=%3Cproquest%3E34049639%3C/proquest%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=34049639&rft_id=info:pmid/&rfr_iscdi=true