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

被引:12
|
作者
Lin, Yan [1 ]
Ong, Yih Ching [1 ]
Keller, Sarah [1 ]
Karges, Johannes [1 ]
Bouchene, Rafika [2 ,3 ]
Manoury, Eric [2 ]
Blacque, Olivier [4 ]
Mueller, Joachim [5 ]
Anghel, Nicoleta [5 ]
Hemphill, Andrew [5 ]
Haberli, Cecile [6 ,7 ]
Taki, Aya C. [8 ]
Gasser, Robin B. [8 ]
Cariou, Kevin [1 ]
Keiser, Jennifer [6 ,7 ]
Gasser, Gilles [1 ]
机构
[1] PSL Univ, Inst Chem Life & Hlth Sci, Lab Inorgan Chem Biol, Chim ParisTech,CNRS, F-75005 Paris, France
[2] Univ Toulouse, LCC Lab Chim Coordinat, CNRS, UPS,INPT, 205 Route Narbonne,BP 44099, F-31077 Toulouse, France
[3] Univ Larbi Ben Mhidi, Fac Sci Exactes, Dept Sci Matiere, BP 358,Route Constantine, Oum El Bouaghi 04000, Algeria
[4] Univ Zurich, Dept Chem, Winterthurerstr 190, CH-8057 Zurich, Switzerland
[5] Univ Bern, Inst Parasitol, Langgass Str 122, CH-3012 Bern, Switzerland
[6] Swiss Trop & Publ Hlth Inst, Dept Med Parasitol & Infect Biol, Socinstr 57, Basel, Switzerland
[7] Univ Basel, Basel, Switzerland
[8] Univ Melbourne, Melbourne Vet Sch, Fac Vet & Agr Sci, Dept Vet Biosci, Parkville, Vic 3010, Australia
基金
澳大利亚研究理事会; 瑞士国家科学基金会;
关键词
IN-VITRO; BENZIMIDAZOLE ANTHELMINTICS; HAEMONCHUS-CONTORTUS; NEOSPORA-CANINUM; COMPLEXES; VIVO; PRAZIQUANTEL; FERROCENYL; TOXICITY;
D O I
10.1039/d0dt01107j
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
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 mu M and no toxicity to mammalian cells (IC50 >100 mu M). 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.
引用
收藏
页码:6616 / 6626
页数:11
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