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Pyclen Tri- n -butylphosphonate Ester as Potential Chelator for Targeted Radiotherapy: From Yttrium(III) Complexation to 90 Y Radiolabeling
The Y3+ complex of PCTMB, the tri-n-butyl phosphonate ester of pyclen (3,6,9,15-tetraazabicyclo[9.3.1]pentadeca-1(15),11,13-triene), was synthesized as well as its Ho3+ and Lu3+ analogues. X-ray diffraction analyses revealed isomorphous dimeric M2(PCTMB)2·9H2O (M = Y, Ho, Lu) structures that crystal...
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Published in: | Inorganic chemistry 2016-08, Vol.55 (16), p.8003-8012 |
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description | The Y3+ complex of PCTMB, the tri-n-butyl phosphonate ester of pyclen (3,6,9,15-tetraazabicyclo[9.3.1]pentadeca-1(15),11,13-triene), was synthesized as well as its Ho3+ and Lu3+ analogues. X-ray diffraction analyses revealed isomorphous dimeric M2(PCTMB)2·9H2O (M = Y, Ho, Lu) structures that crystallize in the centrosymmetric P1 triclinic space group. 1H NMR and UV studies in aqueous solutions indicated that Y3+ complexation is fast, being quantitative in 167 min at pH 3.8 and in 13 min at pH 5.5 (25 °C, acetate buffer, I = 0.150 M, [Y3+] = [PCTMB] = 0.2 mM). 1H NMR DOSY and photon correlation spectroscopy experiments evidenced the formation of aggregates in chloroform with a bimodal distribution that changes slightly with concentration (11-24 and 240-258 nm). The behavior of the acid-assisted dissociation of the complex of Y3+ with PCTMB was studied under pseudo-first-order conditions, and the half-life of the [Y(PCTMB)] complex in 0.5 M HCl at 25 °C was found to be 37 min, a value that decreases to 2.6 min in 5 M HCl. The Y3+ complex of PCTMB is thermodynamically very stable, with a stability constant of log KY-PCTMB = 19.49 and pY = 16.7 measured by potentiometry. 90Y complexation studies revealed fast radiolabeling kinetics; optimal radiolabeling conditions were obtained for 90Y in acetate medium, PCTMB at 10-4 to 10-2 M in acetate buffer pH = 4.75, 15 min at 45-60 °C. In vitro stability studies in human serum showed that [90Y(PCTMB)] is quite stable, with about 90% of the activity still in the form of the radiotracer at 24 h and 80% from 48 h to 72 h. A comparison with other ligands such as PCTA, DOTA, and DTPA already used for in vivo application shows that [90Y(PCTMB)] is an interesting lipophilic and neutral analogue of these reference chelates for therapeutic applications in aqueous and nonaqueous media. © 2016 American Chemical Society. |
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X-ray diffraction analyses revealed isomorphous dimeric M2(PCTMB)2·9H2O (M = Y, Ho, Lu) structures that crystallize in the centrosymmetric P1 triclinic space group. 1H NMR and UV studies in aqueous solutions indicated that Y3+ complexation is fast, being quantitative in 167 min at pH 3.8 and in 13 min at pH 5.5 (25 °C, acetate buffer, I = 0.150 M, [Y3+] = [PCTMB] = 0.2 mM). 1H NMR DOSY and photon correlation spectroscopy experiments evidenced the formation of aggregates in chloroform with a bimodal distribution that changes slightly with concentration (11-24 and 240-258 nm). The behavior of the acid-assisted dissociation of the complex of Y3+ with PCTMB was studied under pseudo-first-order conditions, and the half-life of the [Y(PCTMB)] complex in 0.5 M HCl at 25 °C was found to be 37 min, a value that decreases to 2.6 min in 5 M HCl. The Y3+ complex of PCTMB is thermodynamically very stable, with a stability constant of log KY-PCTMB = 19.49 and pY = 16.7 measured by potentiometry. 90Y complexation studies revealed fast radiolabeling kinetics; optimal radiolabeling conditions were obtained for 90Y in acetate medium, PCTMB at 10-4 to 10-2 M in acetate buffer pH = 4.75, 15 min at 45-60 °C. In vitro stability studies in human serum showed that [90Y(PCTMB)] is quite stable, with about 90% of the activity still in the form of the radiotracer at 24 h and 80% from 48 h to 72 h. A comparison with other ligands such as PCTA, DOTA, and DTPA already used for in vivo application shows that [90Y(PCTMB)] is an interesting lipophilic and neutral analogue of these reference chelates for therapeutic applications in aqueous and nonaqueous media. © 2016 American Chemical Society.</description><identifier>ISSN: 0020-1669</identifier><identifier>EISSN: 1520-510X</identifier><identifier>DOI: 10.1021/acs.inorgchem.6b01135</identifier><identifier>PMID: 27486673</identifier><language>eng</language><publisher>American Chemical Society</publisher><subject>Chemical Sciences ; Coordination chemistry ; Organic chemistry</subject><ispartof>Inorganic chemistry, 2016-08, Vol.55 (16), p.8003-8012</ispartof><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c1321-90ed1f08bc4ebbf4775e11e5348d488e6a669c3e5ec09dde49ae323e20b6911b3</citedby><cites>FETCH-LOGICAL-c1321-90ed1f08bc4ebbf4775e11e5348d488e6a669c3e5ec09dde49ae323e20b6911b3</cites><orcidid>0000-0002-6540-970X ; 0000-0001-9364-788X ; 0000-0001-9860-5451 ; 0000-0002-6989-9654</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttps://hal.univ-brest.fr/hal-01517774$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Le Fur, Mariane</creatorcontrib><creatorcontrib>Beyler, Maryline</creatorcontrib><creatorcontrib>Lepareur, Nicolas</creatorcontrib><creatorcontrib>Fougère, Olivier</creatorcontrib><creatorcontrib>Platas-Iglesias, Carlos</creatorcontrib><creatorcontrib>Rousseaux, Olivier</creatorcontrib><creatorcontrib>Tripier, Raphaël</creatorcontrib><title>Pyclen Tri- n -butylphosphonate Ester as Potential Chelator for Targeted Radiotherapy: From Yttrium(III) Complexation to 90 Y Radiolabeling</title><title>Inorganic chemistry</title><description>The Y3+ complex of PCTMB, the tri-n-butyl phosphonate ester of pyclen (3,6,9,15-tetraazabicyclo[9.3.1]pentadeca-1(15),11,13-triene), was synthesized as well as its Ho3+ and Lu3+ analogues. X-ray diffraction analyses revealed isomorphous dimeric M2(PCTMB)2·9H2O (M = Y, Ho, Lu) structures that crystallize in the centrosymmetric P1 triclinic space group. 1H NMR and UV studies in aqueous solutions indicated that Y3+ complexation is fast, being quantitative in 167 min at pH 3.8 and in 13 min at pH 5.5 (25 °C, acetate buffer, I = 0.150 M, [Y3+] = [PCTMB] = 0.2 mM). 1H NMR DOSY and photon correlation spectroscopy experiments evidenced the formation of aggregates in chloroform with a bimodal distribution that changes slightly with concentration (11-24 and 240-258 nm). The behavior of the acid-assisted dissociation of the complex of Y3+ with PCTMB was studied under pseudo-first-order conditions, and the half-life of the [Y(PCTMB)] complex in 0.5 M HCl at 25 °C was found to be 37 min, a value that decreases to 2.6 min in 5 M HCl. The Y3+ complex of PCTMB is thermodynamically very stable, with a stability constant of log KY-PCTMB = 19.49 and pY = 16.7 measured by potentiometry. 90Y complexation studies revealed fast radiolabeling kinetics; optimal radiolabeling conditions were obtained for 90Y in acetate medium, PCTMB at 10-4 to 10-2 M in acetate buffer pH = 4.75, 15 min at 45-60 °C. In vitro stability studies in human serum showed that [90Y(PCTMB)] is quite stable, with about 90% of the activity still in the form of the radiotracer at 24 h and 80% from 48 h to 72 h. A comparison with other ligands such as PCTA, DOTA, and DTPA already used for in vivo application shows that [90Y(PCTMB)] is an interesting lipophilic and neutral analogue of these reference chelates for therapeutic applications in aqueous and nonaqueous media. © 2016 American Chemical Society.</description><subject>Chemical Sciences</subject><subject>Coordination chemistry</subject><subject>Organic chemistry</subject><issn>0020-1669</issn><issn>1520-510X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><recordid>eNo9kd1Kw0AQhRdRtFYfQdhLe5E6k82vd6WoLRQUqaBXYZNMmpVNtuyuYp_BlzalxYvDDMM5A4ePsRuEKUKId7JyU9Ubu6la6qZJCYgiPmEjjEMIYoT3UzYCGHZMkvyCXTr3CQC5iJJzdhGmUZYkqRix35ddpanna6sC3vOg_PI7vW2NG9RLT_zBebJcOv5iPPVeSc3nLWnpjeXNoLW0G_JU81dZK-NbsnK7u-eP1nT8w3urvrrb5XI54XPTbTX9SK9Mz73hOfCPQ0jLkrTqN1fsrJHa0fVxjtnb48N6vghWz0_L-WwVVChCDHKgGhvIyiqismyiNI0JkWIRZXWUZZTIoXElKKYK8rqmKJckQkEhlEmOWIoxmxz-tlIXW6s6aXeFkapYzFbF_gYYY5qm0TcO3vjgraxxzlLzH0Ao9iCKAUTxD6I4ghB_xkJ_UA</recordid><startdate>20160815</startdate><enddate>20160815</enddate><creator>Le Fur, Mariane</creator><creator>Beyler, Maryline</creator><creator>Lepareur, Nicolas</creator><creator>Fougère, Olivier</creator><creator>Platas-Iglesias, Carlos</creator><creator>Rousseaux, Olivier</creator><creator>Tripier, Raphaël</creator><general>American Chemical Society</general><scope>AAYXX</scope><scope>CITATION</scope><scope>1XC</scope><orcidid>https://orcid.org/0000-0002-6540-970X</orcidid><orcidid>https://orcid.org/0000-0001-9364-788X</orcidid><orcidid>https://orcid.org/0000-0001-9860-5451</orcidid><orcidid>https://orcid.org/0000-0002-6989-9654</orcidid></search><sort><creationdate>20160815</creationdate><title>Pyclen Tri- n -butylphosphonate Ester as Potential Chelator for Targeted Radiotherapy: From Yttrium(III) Complexation to 90 Y Radiolabeling</title><author>Le Fur, Mariane ; Beyler, Maryline ; Lepareur, Nicolas ; Fougère, Olivier ; Platas-Iglesias, Carlos ; Rousseaux, Olivier ; Tripier, Raphaël</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c1321-90ed1f08bc4ebbf4775e11e5348d488e6a669c3e5ec09dde49ae323e20b6911b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Chemical Sciences</topic><topic>Coordination chemistry</topic><topic>Organic chemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Le Fur, Mariane</creatorcontrib><creatorcontrib>Beyler, Maryline</creatorcontrib><creatorcontrib>Lepareur, Nicolas</creatorcontrib><creatorcontrib>Fougère, Olivier</creatorcontrib><creatorcontrib>Platas-Iglesias, Carlos</creatorcontrib><creatorcontrib>Rousseaux, Olivier</creatorcontrib><creatorcontrib>Tripier, Raphaël</creatorcontrib><collection>CrossRef</collection><collection>Hyper Article en Ligne (HAL)</collection><jtitle>Inorganic chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Le Fur, Mariane</au><au>Beyler, Maryline</au><au>Lepareur, Nicolas</au><au>Fougère, Olivier</au><au>Platas-Iglesias, Carlos</au><au>Rousseaux, Olivier</au><au>Tripier, Raphaël</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Pyclen Tri- n -butylphosphonate Ester as Potential Chelator for Targeted Radiotherapy: From Yttrium(III) Complexation to 90 Y Radiolabeling</atitle><jtitle>Inorganic chemistry</jtitle><date>2016-08-15</date><risdate>2016</risdate><volume>55</volume><issue>16</issue><spage>8003</spage><epage>8012</epage><pages>8003-8012</pages><issn>0020-1669</issn><eissn>1520-510X</eissn><abstract>The Y3+ complex of PCTMB, the tri-n-butyl phosphonate ester of pyclen (3,6,9,15-tetraazabicyclo[9.3.1]pentadeca-1(15),11,13-triene), was synthesized as well as its Ho3+ and Lu3+ analogues. X-ray diffraction analyses revealed isomorphous dimeric M2(PCTMB)2·9H2O (M = Y, Ho, Lu) structures that crystallize in the centrosymmetric P1 triclinic space group. 1H NMR and UV studies in aqueous solutions indicated that Y3+ complexation is fast, being quantitative in 167 min at pH 3.8 and in 13 min at pH 5.5 (25 °C, acetate buffer, I = 0.150 M, [Y3+] = [PCTMB] = 0.2 mM). 1H NMR DOSY and photon correlation spectroscopy experiments evidenced the formation of aggregates in chloroform with a bimodal distribution that changes slightly with concentration (11-24 and 240-258 nm). The behavior of the acid-assisted dissociation of the complex of Y3+ with PCTMB was studied under pseudo-first-order conditions, and the half-life of the [Y(PCTMB)] complex in 0.5 M HCl at 25 °C was found to be 37 min, a value that decreases to 2.6 min in 5 M HCl. The Y3+ complex of PCTMB is thermodynamically very stable, with a stability constant of log KY-PCTMB = 19.49 and pY = 16.7 measured by potentiometry. 90Y complexation studies revealed fast radiolabeling kinetics; optimal radiolabeling conditions were obtained for 90Y in acetate medium, PCTMB at 10-4 to 10-2 M in acetate buffer pH = 4.75, 15 min at 45-60 °C. In vitro stability studies in human serum showed that [90Y(PCTMB)] is quite stable, with about 90% of the activity still in the form of the radiotracer at 24 h and 80% from 48 h to 72 h. A comparison with other ligands such as PCTA, DOTA, and DTPA already used for in vivo application shows that [90Y(PCTMB)] is an interesting lipophilic and neutral analogue of these reference chelates for therapeutic applications in aqueous and nonaqueous media. © 2016 American Chemical Society.</abstract><pub>American Chemical Society</pub><pmid>27486673</pmid><doi>10.1021/acs.inorgchem.6b01135</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0002-6540-970X</orcidid><orcidid>https://orcid.org/0000-0001-9364-788X</orcidid><orcidid>https://orcid.org/0000-0001-9860-5451</orcidid><orcidid>https://orcid.org/0000-0002-6989-9654</orcidid></addata></record> |
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subjects | Chemical Sciences Coordination chemistry Organic chemistry |
title | Pyclen Tri- n -butylphosphonate Ester as Potential Chelator for Targeted Radiotherapy: From Yttrium(III) Complexation to 90 Y Radiolabeling |
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