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
Hauptverfasser: 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
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container_end_page 7736
container_issue 24
container_start_page 7730
container_title Journal of the American Chemical Society
container_volume 140
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.
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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. 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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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