Highly Emissive Self-Assembled BODIPY-Platinum Supramolecular Triangles
Light-emitting supramolecular coordination complexes (SCCs) have been widely studied for applications in the chemical and biological sciences. Herein, we report the coordination-driven self-assembly of two highly emissive platinum(II) supramolecular triangles (1 and 2) containing BODIPY-based bridg...
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Veröffentlicht in: | Journal of the American Chemical Society 2018-06, Vol.140 (24), p.7730-7736 |
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creator | Zhou, Jiong Zhang, Yuzhen Yu, Guocan Crawley, Matthew R Fulong, Cressa Ria P Friedman, Alan E Sengupta, Sanghamitra Sun, Jifu Li, Qing Huang, Feihe Cook, Timothy R |
description | Light-emitting supramolecular coordination complexes (SCCs) have been widely studied for applications in the chemical and biological sciences. Herein, we report the coordination-driven self-assembly of two highly emissive platinum(II) supramolecular triangles (1 and 2) containing BODIPY-based bridging ligands. The metallacycles exhibit favorable anticancer activities against HeLa cells (IC50 of 6.41 and 2.11 μM). The characteristic ∼570 nm fluorescence of the boron dipyrromethene (BODIPY) moieties in the metallacycles permits their intracellular visualization using confocal microscopy. Additionally, the BODIPY fluorophore is an excellent photodynamic agent, making the metallacycles as ideal therapeutics for photodynamic therapy (PDT) and chemotherapy. In vitro studies demonstrate that the combination indexes against HeLa cells are 0.56 and 0.48 for 1 and 2, respectively, confirming their synergistic anticancer effect. More importantly, these SCCs also exhibit superior anticancer efficacy toward cisplatin-resistant A2780cis cell line by combining PDT and chemotherapy, showing promise in overcoming drug resistance. This study exploits a multicomponent approach to self-assembled metallacages that enables design of effective theranostic agents wherein the platinum acceptors are toxic chemotherapeutics and the BODIPY donors are imaging probes and photosensitizers. Since each piece may be independently tuned, i.e., Pt(II) polypyridyl fragment swapped for Pt(II) phosphine, the activity may be optimized without a total redesign of the system. |
doi_str_mv | 10.1021/jacs.8b04929 |
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Herein, we report the coordination-driven self-assembly of two highly emissive platinum(II) supramolecular triangles (1 and 2) containing BODIPY-based bridging ligands. The metallacycles exhibit favorable anticancer activities against HeLa cells (IC50 of 6.41 and 2.11 μM). The characteristic ∼570 nm fluorescence of the boron dipyrromethene (BODIPY) moieties in the metallacycles permits their intracellular visualization using confocal microscopy. Additionally, the BODIPY fluorophore is an excellent photodynamic agent, making the metallacycles as ideal therapeutics for photodynamic therapy (PDT) and chemotherapy. In vitro studies demonstrate that the combination indexes against HeLa cells are 0.56 and 0.48 for 1 and 2, respectively, confirming their synergistic anticancer effect. More importantly, these SCCs also exhibit superior anticancer efficacy toward cisplatin-resistant A2780cis cell line by combining PDT and chemotherapy, showing promise in overcoming drug resistance. This study exploits a multicomponent approach to self-assembled metallacages that enables design of effective theranostic agents wherein the platinum acceptors are toxic chemotherapeutics and the BODIPY donors are imaging probes and photosensitizers. Since each piece may be independently tuned, i.e., Pt(II) polypyridyl fragment swapped for Pt(II) phosphine, the activity may be optimized without a total redesign of the system.</description><identifier>ISSN: 0002-7863</identifier><identifier>EISSN: 1520-5126</identifier><identifier>DOI: 10.1021/jacs.8b04929</identifier><identifier>PMID: 29787269</identifier><language>eng</language><publisher>United States: American Chemical Society</publisher><subject>Antineoplastic Agents - chemical synthesis ; Antineoplastic Agents - chemistry ; Antineoplastic Agents - pharmacology ; Antineoplastic Agents - radiation effects ; Apoptosis - drug effects ; Boron Compounds - chemical synthesis ; Boron Compounds - chemistry ; Boron Compounds - pharmacology ; Boron Compounds - radiation effects ; Cell Line, Tumor ; Coordination Complexes - chemical synthesis ; Coordination Complexes - chemistry ; Coordination Complexes - pharmacology ; Coordination Complexes - radiation effects ; Fluorescent Dyes - chemical synthesis ; Fluorescent Dyes - chemistry ; Fluorescent Dyes - pharmacology ; Fluorescent Dyes - radiation effects ; Humans ; Light ; Microscopy, Confocal ; Nanoparticles - chemistry ; Necrosis - chemically induced ; Organoplatinum Compounds - chemical synthesis ; Organoplatinum Compounds - chemistry ; Organoplatinum Compounds - pharmacology ; Organoplatinum Compounds - radiation effects ; Photosensitizing Agents - chemical synthesis ; Photosensitizing Agents - chemistry ; Photosensitizing Agents - pharmacology ; Photosensitizing Agents - radiation effects ; Theranostic Nanomedicine</subject><ispartof>Journal of the American Chemical Society, 2018-06, Vol.140 (24), p.7730-7736</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a324t-f6cb6f7346a8d0b6fb6ed567720d5dbd23691891a58b13aaa6b602e055368b743</citedby><cites>FETCH-LOGICAL-a324t-f6cb6f7346a8d0b6fb6ed567720d5dbd23691891a58b13aaa6b602e055368b743</cites><orcidid>0000-0002-5574-7609 ; 0000-0003-3177-6744 ; 0000-0002-4764-8168 ; 0000-0001-7536-9759 ; 0000-0002-2555-9543 ; 0000-0003-2763-9798 ; 0000-0002-7668-8089</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://pubs.acs.org/doi/pdf/10.1021/jacs.8b04929$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/jacs.8b04929$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>314,780,784,2763,27075,27923,27924,56737,56787</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29787269$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zhou, Jiong</creatorcontrib><creatorcontrib>Zhang, Yuzhen</creatorcontrib><creatorcontrib>Yu, Guocan</creatorcontrib><creatorcontrib>Crawley, Matthew R</creatorcontrib><creatorcontrib>Fulong, Cressa Ria P</creatorcontrib><creatorcontrib>Friedman, Alan E</creatorcontrib><creatorcontrib>Sengupta, Sanghamitra</creatorcontrib><creatorcontrib>Sun, Jifu</creatorcontrib><creatorcontrib>Li, Qing</creatorcontrib><creatorcontrib>Huang, Feihe</creatorcontrib><creatorcontrib>Cook, Timothy R</creatorcontrib><title>Highly Emissive Self-Assembled BODIPY-Platinum Supramolecular Triangles</title><title>Journal of the American Chemical Society</title><addtitle>J. Am. Chem. Soc</addtitle><description>Light-emitting supramolecular coordination complexes (SCCs) have been widely studied for applications in the chemical and biological sciences. Herein, we report the coordination-driven self-assembly of two highly emissive platinum(II) supramolecular triangles (1 and 2) containing BODIPY-based bridging ligands. The metallacycles exhibit favorable anticancer activities against HeLa cells (IC50 of 6.41 and 2.11 μM). The characteristic ∼570 nm fluorescence of the boron dipyrromethene (BODIPY) moieties in the metallacycles permits their intracellular visualization using confocal microscopy. Additionally, the BODIPY fluorophore is an excellent photodynamic agent, making the metallacycles as ideal therapeutics for photodynamic therapy (PDT) and chemotherapy. In vitro studies demonstrate that the combination indexes against HeLa cells are 0.56 and 0.48 for 1 and 2, respectively, confirming their synergistic anticancer effect. More importantly, these SCCs also exhibit superior anticancer efficacy toward cisplatin-resistant A2780cis cell line by combining PDT and chemotherapy, showing promise in overcoming drug resistance. This study exploits a multicomponent approach to self-assembled metallacages that enables design of effective theranostic agents wherein the platinum acceptors are toxic chemotherapeutics and the BODIPY donors are imaging probes and photosensitizers. Since each piece may be independently tuned, i.e., Pt(II) polypyridyl fragment swapped for Pt(II) phosphine, the activity may be optimized without a total redesign of the system.</description><subject>Antineoplastic Agents - chemical synthesis</subject><subject>Antineoplastic Agents - chemistry</subject><subject>Antineoplastic Agents - pharmacology</subject><subject>Antineoplastic Agents - radiation effects</subject><subject>Apoptosis - drug effects</subject><subject>Boron Compounds - chemical synthesis</subject><subject>Boron Compounds - chemistry</subject><subject>Boron Compounds - pharmacology</subject><subject>Boron Compounds - radiation effects</subject><subject>Cell Line, Tumor</subject><subject>Coordination Complexes - chemical synthesis</subject><subject>Coordination Complexes - chemistry</subject><subject>Coordination Complexes - pharmacology</subject><subject>Coordination Complexes - radiation effects</subject><subject>Fluorescent Dyes - chemical synthesis</subject><subject>Fluorescent Dyes - chemistry</subject><subject>Fluorescent Dyes - pharmacology</subject><subject>Fluorescent Dyes - radiation effects</subject><subject>Humans</subject><subject>Light</subject><subject>Microscopy, Confocal</subject><subject>Nanoparticles - chemistry</subject><subject>Necrosis - chemically induced</subject><subject>Organoplatinum Compounds - chemical synthesis</subject><subject>Organoplatinum Compounds - chemistry</subject><subject>Organoplatinum Compounds - pharmacology</subject><subject>Organoplatinum Compounds - radiation effects</subject><subject>Photosensitizing Agents - chemical synthesis</subject><subject>Photosensitizing Agents - chemistry</subject><subject>Photosensitizing Agents - pharmacology</subject><subject>Photosensitizing Agents - radiation effects</subject><subject>Theranostic Nanomedicine</subject><issn>0002-7863</issn><issn>1520-5126</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNptkE1PwkAQhjdGI4jePJsePbi4H92PHhERSEggAQ-emtnuFku2QHatCf_eEtCTp5lJnvfN5EHonpI-JYw-b6CIfW1ImrHsAnWpYAQLyuQl6hJCGFZa8g66iXHTninT9Bp1WKa0YjLrovGkWn_6QzKqqxirb5csnS_xIEZXG-9s8jJ_nS4-8MLDV7Vt6mTZ7APUO--KxkNIVqGC7dq7eIuuSvDR3Z1nD72_jVbDCZ7Nx9PhYIaBs_QLl7IwslQ8laAtaVcjnRVSKUassMYyLjOqMwpCG8oBQBpJmCNCcKmNSnkPPZ16i7CLMbgy34eqhnDIKcmPPvKjj_zso8UfTvi-MbWzf_CvgBZ4PAHH1GbXhG37_f9dP6QKaLc</recordid><startdate>20180620</startdate><enddate>20180620</enddate><creator>Zhou, Jiong</creator><creator>Zhang, Yuzhen</creator><creator>Yu, Guocan</creator><creator>Crawley, Matthew R</creator><creator>Fulong, Cressa Ria P</creator><creator>Friedman, Alan E</creator><creator>Sengupta, Sanghamitra</creator><creator>Sun, Jifu</creator><creator>Li, Qing</creator><creator>Huang, Feihe</creator><creator>Cook, Timothy R</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><orcidid>https://orcid.org/0000-0002-5574-7609</orcidid><orcidid>https://orcid.org/0000-0003-3177-6744</orcidid><orcidid>https://orcid.org/0000-0002-4764-8168</orcidid><orcidid>https://orcid.org/0000-0001-7536-9759</orcidid><orcidid>https://orcid.org/0000-0002-2555-9543</orcidid><orcidid>https://orcid.org/0000-0003-2763-9798</orcidid><orcidid>https://orcid.org/0000-0002-7668-8089</orcidid></search><sort><creationdate>20180620</creationdate><title>Highly Emissive Self-Assembled BODIPY-Platinum Supramolecular Triangles</title><author>Zhou, Jiong ; Zhang, Yuzhen ; Yu, Guocan ; Crawley, Matthew R ; Fulong, Cressa Ria P ; Friedman, Alan E ; Sengupta, Sanghamitra ; Sun, Jifu ; Li, Qing ; Huang, Feihe ; Cook, Timothy R</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a324t-f6cb6f7346a8d0b6fb6ed567720d5dbd23691891a58b13aaa6b602e055368b743</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Antineoplastic Agents - chemical synthesis</topic><topic>Antineoplastic Agents - chemistry</topic><topic>Antineoplastic Agents - pharmacology</topic><topic>Antineoplastic Agents - radiation effects</topic><topic>Apoptosis - drug effects</topic><topic>Boron Compounds - chemical synthesis</topic><topic>Boron Compounds - chemistry</topic><topic>Boron Compounds - pharmacology</topic><topic>Boron Compounds - radiation effects</topic><topic>Cell Line, Tumor</topic><topic>Coordination Complexes - chemical synthesis</topic><topic>Coordination Complexes - chemistry</topic><topic>Coordination Complexes - pharmacology</topic><topic>Coordination Complexes - radiation effects</topic><topic>Fluorescent Dyes - chemical synthesis</topic><topic>Fluorescent Dyes - chemistry</topic><topic>Fluorescent Dyes - pharmacology</topic><topic>Fluorescent Dyes - radiation effects</topic><topic>Humans</topic><topic>Light</topic><topic>Microscopy, Confocal</topic><topic>Nanoparticles - chemistry</topic><topic>Necrosis - chemically induced</topic><topic>Organoplatinum Compounds - chemical synthesis</topic><topic>Organoplatinum Compounds - chemistry</topic><topic>Organoplatinum Compounds - pharmacology</topic><topic>Organoplatinum Compounds - radiation effects</topic><topic>Photosensitizing Agents - chemical synthesis</topic><topic>Photosensitizing Agents - chemistry</topic><topic>Photosensitizing Agents - pharmacology</topic><topic>Photosensitizing Agents - radiation effects</topic><topic>Theranostic Nanomedicine</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zhou, Jiong</creatorcontrib><creatorcontrib>Zhang, Yuzhen</creatorcontrib><creatorcontrib>Yu, Guocan</creatorcontrib><creatorcontrib>Crawley, Matthew R</creatorcontrib><creatorcontrib>Fulong, Cressa Ria P</creatorcontrib><creatorcontrib>Friedman, Alan E</creatorcontrib><creatorcontrib>Sengupta, Sanghamitra</creatorcontrib><creatorcontrib>Sun, Jifu</creatorcontrib><creatorcontrib>Li, Qing</creatorcontrib><creatorcontrib>Huang, Feihe</creatorcontrib><creatorcontrib>Cook, Timothy R</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><jtitle>Journal of the American Chemical Society</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zhou, Jiong</au><au>Zhang, Yuzhen</au><au>Yu, Guocan</au><au>Crawley, Matthew R</au><au>Fulong, Cressa Ria P</au><au>Friedman, Alan E</au><au>Sengupta, Sanghamitra</au><au>Sun, Jifu</au><au>Li, Qing</au><au>Huang, Feihe</au><au>Cook, Timothy R</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Highly Emissive Self-Assembled BODIPY-Platinum Supramolecular Triangles</atitle><jtitle>Journal of the American Chemical Society</jtitle><addtitle>J. Am. Chem. Soc</addtitle><date>2018-06-20</date><risdate>2018</risdate><volume>140</volume><issue>24</issue><spage>7730</spage><epage>7736</epage><pages>7730-7736</pages><issn>0002-7863</issn><eissn>1520-5126</eissn><abstract>Light-emitting supramolecular coordination complexes (SCCs) have been widely studied for applications in the chemical and biological sciences. Herein, we report the coordination-driven self-assembly of two highly emissive platinum(II) supramolecular triangles (1 and 2) containing BODIPY-based bridging ligands. The metallacycles exhibit favorable anticancer activities against HeLa cells (IC50 of 6.41 and 2.11 μM). The characteristic ∼570 nm fluorescence of the boron dipyrromethene (BODIPY) moieties in the metallacycles permits their intracellular visualization using confocal microscopy. Additionally, the BODIPY fluorophore is an excellent photodynamic agent, making the metallacycles as ideal therapeutics for photodynamic therapy (PDT) and chemotherapy. In vitro studies demonstrate that the combination indexes against HeLa cells are 0.56 and 0.48 for 1 and 2, respectively, confirming their synergistic anticancer effect. More importantly, these SCCs also exhibit superior anticancer efficacy toward cisplatin-resistant A2780cis cell line by combining PDT and chemotherapy, showing promise in overcoming drug resistance. This study exploits a multicomponent approach to self-assembled metallacages that enables design of effective theranostic agents wherein the platinum acceptors are toxic chemotherapeutics and the BODIPY donors are imaging probes and photosensitizers. Since each piece may be independently tuned, i.e., Pt(II) polypyridyl fragment swapped for Pt(II) phosphine, the activity may be optimized without a total redesign of the system.</abstract><cop>United States</cop><pub>American Chemical Society</pub><pmid>29787269</pmid><doi>10.1021/jacs.8b04929</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0002-5574-7609</orcidid><orcidid>https://orcid.org/0000-0003-3177-6744</orcidid><orcidid>https://orcid.org/0000-0002-4764-8168</orcidid><orcidid>https://orcid.org/0000-0001-7536-9759</orcidid><orcidid>https://orcid.org/0000-0002-2555-9543</orcidid><orcidid>https://orcid.org/0000-0003-2763-9798</orcidid><orcidid>https://orcid.org/0000-0002-7668-8089</orcidid></addata></record> |
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subjects | Antineoplastic Agents - chemical synthesis Antineoplastic Agents - chemistry Antineoplastic Agents - pharmacology Antineoplastic Agents - radiation effects Apoptosis - drug effects Boron Compounds - chemical synthesis Boron Compounds - chemistry Boron Compounds - pharmacology Boron Compounds - radiation effects Cell Line, Tumor Coordination Complexes - chemical synthesis Coordination Complexes - chemistry Coordination Complexes - pharmacology Coordination Complexes - radiation effects Fluorescent Dyes - chemical synthesis Fluorescent Dyes - chemistry Fluorescent Dyes - pharmacology Fluorescent Dyes - radiation effects Humans Light Microscopy, Confocal Nanoparticles - chemistry Necrosis - chemically induced Organoplatinum Compounds - chemical synthesis Organoplatinum Compounds - chemistry Organoplatinum Compounds - pharmacology Organoplatinum Compounds - radiation effects Photosensitizing Agents - chemical synthesis Photosensitizing Agents - chemistry Photosensitizing Agents - pharmacology Photosensitizing Agents - radiation effects Theranostic Nanomedicine |
title | Highly Emissive Self-Assembled BODIPY-Platinum Supramolecular Triangles |
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