Increasing the π-Expansive Ligands in Ruthenium(II) Polypyridyl Complexes: Synthesis, Characterization, and Biological Evaluation for Photodynamic Therapy Applications.


Journal

Inorganic chemistry
ISSN: 1520-510X
Titre abrégé: Inorg Chem
Pays: United States
ID NLM: 0366543

Informations de publication

Date de publication:
13 Nov 2023
Historique:
medline: 14 11 2023
pubmed: 2 11 2023
entrez: 1 11 2023
Statut: ppublish

Résumé

Lack of selectivity is one of the main issues with currently used chemotherapies, causing damage not only to altered cells but also to healthy cells. Over the last decades, photodynamic therapy (PDT) has increased as a promising therapeutic tool due to its potential to treat diseases like cancer or bacterial infections with a high spatiotemporal control. Ruthenium(II) polypyridyl compounds are gaining attention for their application as photosensitizers (PSs) since they are generally nontoxic in dark conditions, while they show remarkable toxicity after light irradiation. In this work, four Ru(II) polypyridyl compounds with sterically expansive ligands were studied as PDT agents. The Ru(II) complexes were synthesized using an alternative route to those described in the literature, which resulted in an improvement of the synthesis yields. Solid-state structures of compounds

Identifiants

pubmed: 37913550
doi: 10.1021/acs.inorgchem.3c02606
doi:

Substances chimiques

Coordination Complexes 0
Ruthenium 7UI0TKC3U5
Singlet Oxygen 17778-80-2
DNA 9007-49-2
Ligands 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

18510-18523

Auteurs

Maria Dalla Pozza (MD)

Chimie ParisTech, PSL University, CNRS, Institute of Chemistry for Life and Health, Paris 75005, France.

Pierre Mesdom (P)

Chimie ParisTech, PSL University, CNRS, Institute of Chemistry for Life and Health, Paris 75005, France.

Ahmad Abdullrahman (A)

Department of Pharmacy, Chemistry and Pharmacy Building, University of Reading, Whiteknights Campus, Reading, Berkshire RG6 6AD, U.K.

Tayler D Prieto Otoya (TD)

Department of Chemistry, University of Reading, Whiteknights, Reading RG6 6AD, U.K.

Philippe Arnoux (P)

Université de Lorraine, CNRS, LRGP, Nancy F-54000, France.

Céline Frochot (C)

Université de Lorraine, CNRS, LRGP, Nancy F-54000, France.

Germain Niogret (G)

Institut Pasteur, Université Paris Cité, CNRS UMR3523, Departement of Structural Biology and Chemistry, Laboratory for Bioorganic Chemistry of Nucleic Acids, Paris 75015, France.

Bruno Saubaméa (B)

Université Paris Cité, INSERM, CNRS, P-MIM, Plateforme d'Imagerie Cellulaire et Moléculaire (PICMO), Paris F-75006, France.

Pierre Burckel (P)

Université de Paris, Institut de physique du globe de Paris, CNRS, Paris F-75005, France.

James P Hall (JP)

Department of Pharmacy, Chemistry and Pharmacy Building, University of Reading, Whiteknights Campus, Reading, Berkshire RG6 6AD, U.K.

Marcel Hollenstein (M)

Institut Pasteur, Université Paris Cité, CNRS UMR3523, Departement of Structural Biology and Chemistry, Laboratory for Bioorganic Chemistry of Nucleic Acids, Paris 75015, France.

Christine J Cardin (CJ)

Department of Chemistry, University of Reading, Whiteknights, Reading RG6 6AD, U.K.

Gilles Gasser (G)

Chimie ParisTech, PSL University, CNRS, Institute of Chemistry for Life and Health, Paris 75005, France.

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Classifications MeSH