Synthesis, characterization and antiparasitic activity of organometallic derivatives of the anthelmintic drug albendazole.
Albendazole
/ chemical synthesis
Animals
Anthelmintics
/ chemical synthesis
Dose-Response Relationship, Drug
Female
Giardia lamblia
/ drug effects
Haemonchus
/ drug effects
Mice
Mice, Inbred C57BL
Molecular Structure
Nematospiroides dubius
/ drug effects
Parasitic Sensitivity Tests
Schistosoma mansoni
/ drug effects
Structure-Activity Relationship
Toxoplasma
/ drug effects
Trichuris
/ drug effects
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
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.
Substances chimiques
Anthelmintics
0
Albendazole
F4216019LN
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM