Novel Arsenic Nanoparticles Are More Effective and Less Toxic than As (III) to Inhibit Extracellular and Intracellular Proliferation of Leishmania donovani

Visceral leishmaniasis, a vector-borne tropical disease that is threatening about 350 million people worldwide, is caused by the protozoan parasite Leishmania donovani. Metalloids like arsenic and antimony have been used to treat diseases like leishmaniasis caused by the kinetoplastid parasites. Ars...

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Main Authors: Sudipta Chakraborty, Kaushik Bhar, Sandip Saha, Rajarshi Chakrabarti, Anjali Pal, Anirban Siddhanta
Format: Article
Language:English
Published: Wiley 2014-01-01
Series:Journal of Parasitology Research
Online Access:http://dx.doi.org/10.1155/2014/187640
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author Sudipta Chakraborty
Kaushik Bhar
Sandip Saha
Rajarshi Chakrabarti
Anjali Pal
Anirban Siddhanta
author_facet Sudipta Chakraborty
Kaushik Bhar
Sandip Saha
Rajarshi Chakrabarti
Anjali Pal
Anirban Siddhanta
author_sort Sudipta Chakraborty
collection DOAJ
description Visceral leishmaniasis, a vector-borne tropical disease that is threatening about 350 million people worldwide, is caused by the protozoan parasite Leishmania donovani. Metalloids like arsenic and antimony have been used to treat diseases like leishmaniasis caused by the kinetoplastid parasites. Arsenic (III) at a relatively higher concentration (30 μg/mL) has been shown to have antileishmanial activity, but this concentration is reported to be toxic in several experimental mammalian systems. Nanosized metal (0) particles have been shown to be more effective than their higher oxidation state forms. There is no information so far regarding arsenic nanoparticles (As-NPs) as an antileishmanial agent. We have tested the antileishmanial properties of the As-NPs, developed for the first time in our laboratory. As-NPs inhibited the in vitro growth, oxygen consumption, infectivity, and intramacrophage proliferation of L. donovani parasites at a concentration which is about several fold lower than that of As (III). Moreover, this antileishmanial activity has comparatively less cytotoxic effect on the mouse macrophage cell line. It is evident from our findings that As-NPs have more potential than As (III) to be used as an antileishmanial agent.
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institution Kabale University
issn 2090-0023
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publishDate 2014-01-01
publisher Wiley
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series Journal of Parasitology Research
spelling doaj-art-2d54fe7aba7c4895affa34e695cc42242025-02-03T01:12:09ZengWileyJournal of Parasitology Research2090-00232090-00312014-01-01201410.1155/2014/187640187640Novel Arsenic Nanoparticles Are More Effective and Less Toxic than As (III) to Inhibit Extracellular and Intracellular Proliferation of Leishmania donovaniSudipta Chakraborty0Kaushik Bhar1Sandip Saha2Rajarshi Chakrabarti3Anjali Pal4Anirban Siddhanta5Department of Biochemistry, University of Calcutta, Kolkata 700019, IndiaDepartment of Biochemistry, University of Calcutta, Kolkata 700019, IndiaDepartment of Civil Engineering, Indian Institute of Technology, Kharagpur 721302, IndiaDepartment of Biochemistry, University of Calcutta, Kolkata 700019, IndiaDepartment of Civil Engineering, Indian Institute of Technology, Kharagpur 721302, IndiaDepartment of Biochemistry, University of Calcutta, Kolkata 700019, IndiaVisceral leishmaniasis, a vector-borne tropical disease that is threatening about 350 million people worldwide, is caused by the protozoan parasite Leishmania donovani. Metalloids like arsenic and antimony have been used to treat diseases like leishmaniasis caused by the kinetoplastid parasites. Arsenic (III) at a relatively higher concentration (30 μg/mL) has been shown to have antileishmanial activity, but this concentration is reported to be toxic in several experimental mammalian systems. Nanosized metal (0) particles have been shown to be more effective than their higher oxidation state forms. There is no information so far regarding arsenic nanoparticles (As-NPs) as an antileishmanial agent. We have tested the antileishmanial properties of the As-NPs, developed for the first time in our laboratory. As-NPs inhibited the in vitro growth, oxygen consumption, infectivity, and intramacrophage proliferation of L. donovani parasites at a concentration which is about several fold lower than that of As (III). Moreover, this antileishmanial activity has comparatively less cytotoxic effect on the mouse macrophage cell line. It is evident from our findings that As-NPs have more potential than As (III) to be used as an antileishmanial agent.http://dx.doi.org/10.1155/2014/187640
spellingShingle Sudipta Chakraborty
Kaushik Bhar
Sandip Saha
Rajarshi Chakrabarti
Anjali Pal
Anirban Siddhanta
Novel Arsenic Nanoparticles Are More Effective and Less Toxic than As (III) to Inhibit Extracellular and Intracellular Proliferation of Leishmania donovani
Journal of Parasitology Research
title Novel Arsenic Nanoparticles Are More Effective and Less Toxic than As (III) to Inhibit Extracellular and Intracellular Proliferation of Leishmania donovani
title_full Novel Arsenic Nanoparticles Are More Effective and Less Toxic than As (III) to Inhibit Extracellular and Intracellular Proliferation of Leishmania donovani
title_fullStr Novel Arsenic Nanoparticles Are More Effective and Less Toxic than As (III) to Inhibit Extracellular and Intracellular Proliferation of Leishmania donovani
title_full_unstemmed Novel Arsenic Nanoparticles Are More Effective and Less Toxic than As (III) to Inhibit Extracellular and Intracellular Proliferation of Leishmania donovani
title_short Novel Arsenic Nanoparticles Are More Effective and Less Toxic than As (III) to Inhibit Extracellular and Intracellular Proliferation of Leishmania donovani
title_sort novel arsenic nanoparticles are more effective and less toxic than as iii to inhibit extracellular and intracellular proliferation of leishmania donovani
url http://dx.doi.org/10.1155/2014/187640
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