Synthesis, characterization and antiparasitic activity of organometallic derivatives of the anthelmintic drug albendazole.


Journal

Dalton transactions (Cambridge, England : 2003)
ISSN: 1477-9234
Titre abrégé: Dalton Trans
Pays: England
ID NLM: 101176026

Informations de publication

Date de publication:
26 May 2020
Historique:
pubmed: 30 4 2020
medline: 15 1 2021
entrez: 30 4 2020
Statut: ppublish

Résumé

Helminthiases, a group of neglected tropical diseases, affect more than one billion people mainly in tropical and subtropical regions. Moreover, major intestinal protozoa have a significant impact on global public health. Albendazole (ABZ) is a broad-spectrum anthelmintic recommended by the World Health Organisation (WHO). However, drug resistance is emerging due to its widespread use. In order to tackle this problem, taking into account the spectacular results obtained with ferroquine, an organometallic derivatization of the antimalarial drug chloroquine, we have prepared, in this study, a series of new ferrocenyl and ruthenocenyl derivatives of the organic drug ABZ and assessed their activity against different helminths and protozoans, namely Trichuris muris, Heligmosomoides polygygrus, Schistosoma mansoni, Giardia lamblia, Haemonchus contortus and Toxoplasma gondii. The ferrocene-containing ABZ analogue 2d exhibited over 70% activity against T. muris adults in vitro at 200 μM and no toxicity to mammalian cells (IC50 >100 μM). H. polygyrus adults were not affected by any of the derivatives tested. Against T. gondii, the ferrocene-containing ABZ analogues 1a and 2d showed better in vitro activity than ABZ and low toxicity to the host cells. The activity of the analogous ruthenocenyl compound 2b against S. mansoni and T. gondii in vitro might be attributed to its toxicity towards the host cells rather than a specific antiparasitic activity. These results demonstrate that the derivatives show a species specific in vitro activity and the choice of the organometallic moieties attached to the organic drug is playing a very important role. Two of our organometallic compounds, namely 1b and 2d, were tested in T. muris infected mice. At a 400 mg kg-1 dose, the compounds showed moderate worm burden reductions but low worm expulsion rates. Overall, this work, which is one of the first studies reporting the potential of organometallic compounds on a very broad range of parasitic helminths and protozoan, is a clear confirmation of the potential of organometallic complexes against parasites of medical and veterinary importance.

Identifiants

pubmed: 32347259
doi: 10.1039/d0dt01107j
doi:

Substances chimiques

Anthelmintics 0
Albendazole F4216019LN

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

6616-6626

Auteurs

Yan Lin (Y)

Chimie ParisTech, PSL University, CNRS, Institute of Chemistry for Life and Health Sciences, Laboratory for Inorganic Chemical Biology, 75005 Paris, France. kevin.cariou@cnrs.fr gilles.gasser@chimieparistech.psl.eu.

Yih Ching Ong (YC)

Chimie ParisTech, PSL University, CNRS, Institute of Chemistry for Life and Health Sciences, Laboratory for Inorganic Chemical Biology, 75005 Paris, France. kevin.cariou@cnrs.fr gilles.gasser@chimieparistech.psl.eu.

Sarah Keller (S)

Chimie ParisTech, PSL University, CNRS, Institute of Chemistry for Life and Health Sciences, Laboratory for Inorganic Chemical Biology, 75005 Paris, France. kevin.cariou@cnrs.fr gilles.gasser@chimieparistech.psl.eu.

Johannes Karges (J)

Chimie ParisTech, PSL University, CNRS, Institute of Chemistry for Life and Health Sciences, Laboratory for Inorganic Chemical Biology, 75005 Paris, France. kevin.cariou@cnrs.fr gilles.gasser@chimieparistech.psl.eu.

Rafika Bouchene (R)

CNRS, LCC (Laboratoire de Chimie de Coordination), Université de Toulouse, UPS, INPT, 205 Route de Narbonne, BP 44099, 31077 Toulouse, France and Département Sciences de la Matière, Faculté des Sciences Exactes, Université Larbi Ben M'hidi, BP 358, Route de Constantine, 04000 Oum El Bouaghi, Algeria.

Eric Manoury (E)

CNRS, LCC (Laboratoire de Chimie de Coordination), Université de Toulouse, UPS, INPT, 205 Route de Narbonne, BP 44099, 31077 Toulouse, France.

Olivier Blacque (O)

Department of Chemistry, University of Zurich, Winterthurerstrasse 190, 8057 Zurich, Switzerland.

Joachim Müller (J)

Institute of Parasitology, University of Bern, Länggass-Strasse 122, 3012 Bern, Switzerland.

Nicoleta Anghel (N)

Institute of Parasitology, University of Bern, Länggass-Strasse 122, 3012 Bern, Switzerland.

Andrew Hemphill (A)

Institute of Parasitology, University of Bern, Länggass-Strasse 122, 3012 Bern, Switzerland.

Cécile Häberli (C)

Department of Medical Parasitology and Infection Biology, Swiss Tropical and Public Health Institute, Socinstr. 57, Basel, Switzerland. jennifer.keiser@swisstph.ch and University of Basel, Basel, Switzerland.

Aya C Taki (AC)

Department of Veterinary Biosciences, Melbourne Veterinary School, Faculty of Veterinary and Agricultural Sciences, The University of Melbourne, Parkville, Victoria 3010, Australia.

Robin B Gasser (RB)

Department of Veterinary Biosciences, Melbourne Veterinary School, Faculty of Veterinary and Agricultural Sciences, The University of Melbourne, Parkville, Victoria 3010, Australia.

Kevin Cariou (K)

Chimie ParisTech, PSL University, CNRS, Institute of Chemistry for Life and Health Sciences, Laboratory for Inorganic Chemical Biology, 75005 Paris, France. kevin.cariou@cnrs.fr gilles.gasser@chimieparistech.psl.eu.

Jennifer Keiser (J)

Department of Medical Parasitology and Infection Biology, Swiss Tropical and Public Health Institute, Socinstr. 57, Basel, Switzerland. jennifer.keiser@swisstph.ch and University of Basel, Basel, Switzerland.

Gilles Gasser (G)

Chimie ParisTech, PSL University, CNRS, Institute of Chemistry for Life and Health Sciences, Laboratory for Inorganic Chemical Biology, 75005 Paris, France. kevin.cariou@cnrs.fr gilles.gasser@chimieparistech.psl.eu.

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