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Gd(iii)–Pt(iv) theranostic contrast agents for tandem MR imaging and chemotherapy

Pt(iv) prodrugs have emerged as versatile therapeutics for addressing issues regarding off-target toxicity and the chemoresistance of classic Pt(ii) drugs such as cisplatin and carboplatin. There is significant potential for Pt(iv) complexes to be used as theranostic agents, yet there are currently...

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Autores principales: Adams, Casey J., Meade, Thomas J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8157322/
https://www.ncbi.nlm.nih.gov/pubmed/34084418
http://dx.doi.org/10.1039/c9sc05937g
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author Adams, Casey J.
Meade, Thomas J.
author_facet Adams, Casey J.
Meade, Thomas J.
author_sort Adams, Casey J.
collection PubMed
description Pt(iv) prodrugs have emerged as versatile therapeutics for addressing issues regarding off-target toxicity and the chemoresistance of classic Pt(ii) drugs such as cisplatin and carboplatin. There is significant potential for Pt(iv) complexes to be used as theranostic agents, yet there are currently no reported examples of Gd(iii)–Pt(iv) agents for simultaneous MR imaging and chemotherapy. Here we report the synthesis, characterization, and in vitro efficacy of two Gd(iii)–Pt(iv) agents, GP1 and GP2. Both agents are water soluble and stable under extracellularly relevant conditions but are reduced under intracellular conditions. Both are cytotoxic in multiple cancer cell lines, cell permeable, and significantly enhance the T(1)-weighted MR contrast of multiple cell lines. Thus, GP1 and GP2 are promising agents for tandem MR imaging and chemotherapy and provide a versatile platform through which future Gd(iii)–Pt(iv) agents can be developed.
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spelling pubmed-81573222021-06-02 Gd(iii)–Pt(iv) theranostic contrast agents for tandem MR imaging and chemotherapy Adams, Casey J. Meade, Thomas J. Chem Sci Chemistry Pt(iv) prodrugs have emerged as versatile therapeutics for addressing issues regarding off-target toxicity and the chemoresistance of classic Pt(ii) drugs such as cisplatin and carboplatin. There is significant potential for Pt(iv) complexes to be used as theranostic agents, yet there are currently no reported examples of Gd(iii)–Pt(iv) agents for simultaneous MR imaging and chemotherapy. Here we report the synthesis, characterization, and in vitro efficacy of two Gd(iii)–Pt(iv) agents, GP1 and GP2. Both agents are water soluble and stable under extracellularly relevant conditions but are reduced under intracellular conditions. Both are cytotoxic in multiple cancer cell lines, cell permeable, and significantly enhance the T(1)-weighted MR contrast of multiple cell lines. Thus, GP1 and GP2 are promising agents for tandem MR imaging and chemotherapy and provide a versatile platform through which future Gd(iii)–Pt(iv) agents can be developed. The Royal Society of Chemistry 2020-01-28 /pmc/articles/PMC8157322/ /pubmed/34084418 http://dx.doi.org/10.1039/c9sc05937g Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/
spellingShingle Chemistry
Adams, Casey J.
Meade, Thomas J.
Gd(iii)–Pt(iv) theranostic contrast agents for tandem MR imaging and chemotherapy
title Gd(iii)–Pt(iv) theranostic contrast agents for tandem MR imaging and chemotherapy
title_full Gd(iii)–Pt(iv) theranostic contrast agents for tandem MR imaging and chemotherapy
title_fullStr Gd(iii)–Pt(iv) theranostic contrast agents for tandem MR imaging and chemotherapy
title_full_unstemmed Gd(iii)–Pt(iv) theranostic contrast agents for tandem MR imaging and chemotherapy
title_short Gd(iii)–Pt(iv) theranostic contrast agents for tandem MR imaging and chemotherapy
title_sort gd(iii)–pt(iv) theranostic contrast agents for tandem mr imaging and chemotherapy
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8157322/
https://www.ncbi.nlm.nih.gov/pubmed/34084418
http://dx.doi.org/10.1039/c9sc05937g
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