Study of Cytotoxic and Photodynamic Activities of Dyads Composed of a Zinc Phthalocyanine Appended to an Organotin.

chemotherapy photodynamic therapy tin complex zinc (II) phthalocyanine

Journal

Pharmaceuticals (Basel, Switzerland)
ISSN: 1424-8247
Titre abrégé: Pharmaceuticals (Basel)
Pays: Switzerland
ID NLM: 101238453

Informations de publication

Date de publication:
28 Apr 2021
Historique:
received: 06 04 2021
accepted: 19 04 2021
entrez: 30 4 2021
pubmed: 1 5 2021
medline: 1 5 2021
Statut: epublish

Résumé

The combination of photodynamic therapy and chemotherapy is a promising strategy to enhance cancer therapeutic efficacy and reduce drug resistance. In this study two zinc(II) phthalocyanine-tin(IV) conjugates linked by a triethylene glycol chain were synthesized and characterized. In these complexes, the zinc(II) phthalocyanine was used as a potential photosensitizer for PDT and the tin complex was selected as cytostatic moiety. The two dyads composed of zinc(II) phthalocyanine and tin complexes exhibited high cytotoxicity, in absence of light stimulation, against MCF-7 human breast cancer cells with low LC

Identifiants

pubmed: 33924752
pii: ph14050413
doi: 10.3390/ph14050413
pmc: PMC8145453
pii:
doi:

Types de publication

Journal Article

Langues

eng

Subventions

Organisme : Campus France
ID : Eiffel grant
Organisme : Conseil régionnal Pays de la Loire
ID : Lumomat
Organisme : CNRS-L
ID : IT fellowship
Organisme : Lebanese University
ID : IT fellowship

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Auteurs

Isabelle Toubia (I)

CEISAM, Chimie Et Interdisciplinarité, Synthèse, Analyse, Modélisation, CNRS, UMR CNRS 6230, Université de Nantes, 2, rue de la Houssinière-BP 92208, CEDEX 3, 44322 Nantes, France.
LRGP, Laboratoire Réactions et Génie des Procédés, UMR 7274 CNRS-Université de Lorraine, 1 rue Grandville, 54000 Nancy, France.

Christophe Nguyen (C)

IBMM, Université de Montpellier, CNRS, ENSCM, 34093 Montpellier, France.

Stéphane Diring (S)

CEISAM, Chimie Et Interdisciplinarité, Synthèse, Analyse, Modélisation, CNRS, UMR CNRS 6230, Université de Nantes, 2, rue de la Houssinière-BP 92208, CEDEX 3, 44322 Nantes, France.

Marine Pays (M)

IBMM, Université de Montpellier, CNRS, ENSCM, 34093 Montpellier, France.

Elodie Mattana (E)

IBMM, Université de Montpellier, CNRS, ENSCM, 34093 Montpellier, France.

Philippe Arnoux (P)

LRGP, Laboratoire Réactions et Génie des Procédés, UMR 7274 CNRS-Université de Lorraine, 1 rue Grandville, 54000 Nancy, France.

Céline Frochot (C)

LRGP, Laboratoire Réactions et Génie des Procédés, UMR 7274 CNRS-Université de Lorraine, 1 rue Grandville, 54000 Nancy, France.

Magali Gary-Bobo (M)

IBMM, Université de Montpellier, CNRS, ENSCM, 34093 Montpellier, France.

Marwan Kobeissi (M)

Laboratoire Rammal Rammal, Equipe de Synthèse Organique Appliquée SOA, Faculté des Sciences 5, Université Libanaise, Nabatieh, Lebanon.

Fabrice Odobel (F)

CEISAM, Chimie Et Interdisciplinarité, Synthèse, Analyse, Modélisation, CNRS, UMR CNRS 6230, Université de Nantes, 2, rue de la Houssinière-BP 92208, CEDEX 3, 44322 Nantes, France.

Classifications MeSH