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Polyanhydride Nanoparticle Delivery Platform Dramatically Enhances Killing of Filarial Worms

Filarial diseases represent a significant social and economic burden to over 120 million people worldwide and are caused by endoparasites that require the presence of symbiotic bacteria of the genus Wolbachia for fertility and viability of the host parasite. Targeting Wolbachia for elimination is a...

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Autores principales: Binnebose, Andrea M., Haughney, Shannon L., Martin, Richard, Imerman, Paula M., Narasimhan, Balaji, Bellaire, Bryan H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4619673/
https://www.ncbi.nlm.nih.gov/pubmed/26496201
http://dx.doi.org/10.1371/journal.pntd.0004173
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author Binnebose, Andrea M.
Haughney, Shannon L.
Martin, Richard
Imerman, Paula M.
Narasimhan, Balaji
Bellaire, Bryan H.
author_facet Binnebose, Andrea M.
Haughney, Shannon L.
Martin, Richard
Imerman, Paula M.
Narasimhan, Balaji
Bellaire, Bryan H.
author_sort Binnebose, Andrea M.
collection PubMed
description Filarial diseases represent a significant social and economic burden to over 120 million people worldwide and are caused by endoparasites that require the presence of symbiotic bacteria of the genus Wolbachia for fertility and viability of the host parasite. Targeting Wolbachia for elimination is a therapeutic approach that shows promise in the treatment of onchocerciasis and lymphatic filariasis. Here we demonstrate the use of a biodegradable polyanhydride nanoparticle-based platform for the co-delivery of the antibiotic doxycycline with the antiparasitic drug, ivermectin, to reduce microfilarial burden and rapidly kill adult worms. When doxycycline and ivermectin were co-delivered within polyanhydride nanoparticles, effective killing of adult female Brugia malayi filarial worms was achieved with approximately 4,000-fold reduction in the amount of drug used. Additionally the time to death of the macrofilaria was also significantly reduced (five-fold) when the anti-filarial drug cocktail was delivered within polyanhydride nanoparticles. We hypothesize that the mechanism behind this dramatically enhanced killing of the macrofilaria is the ability of the polyanhydride nanoparticles to behave as a Trojan horse and penetrate the cuticle, bypassing excretory pumps of B. malayi, and effectively deliver drug directly to both the worm and Wolbachia at high enough microenvironmental concentrations to cause death. These provocative findings may have significant consequences for the reduction in the amount of drug and the length of treatment required for filarial infections in terms of patient compliance and reduced cost of treatment.
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spelling pubmed-46196732015-10-29 Polyanhydride Nanoparticle Delivery Platform Dramatically Enhances Killing of Filarial Worms Binnebose, Andrea M. Haughney, Shannon L. Martin, Richard Imerman, Paula M. Narasimhan, Balaji Bellaire, Bryan H. PLoS Negl Trop Dis Research Article Filarial diseases represent a significant social and economic burden to over 120 million people worldwide and are caused by endoparasites that require the presence of symbiotic bacteria of the genus Wolbachia for fertility and viability of the host parasite. Targeting Wolbachia for elimination is a therapeutic approach that shows promise in the treatment of onchocerciasis and lymphatic filariasis. Here we demonstrate the use of a biodegradable polyanhydride nanoparticle-based platform for the co-delivery of the antibiotic doxycycline with the antiparasitic drug, ivermectin, to reduce microfilarial burden and rapidly kill adult worms. When doxycycline and ivermectin were co-delivered within polyanhydride nanoparticles, effective killing of adult female Brugia malayi filarial worms was achieved with approximately 4,000-fold reduction in the amount of drug used. Additionally the time to death of the macrofilaria was also significantly reduced (five-fold) when the anti-filarial drug cocktail was delivered within polyanhydride nanoparticles. We hypothesize that the mechanism behind this dramatically enhanced killing of the macrofilaria is the ability of the polyanhydride nanoparticles to behave as a Trojan horse and penetrate the cuticle, bypassing excretory pumps of B. malayi, and effectively deliver drug directly to both the worm and Wolbachia at high enough microenvironmental concentrations to cause death. These provocative findings may have significant consequences for the reduction in the amount of drug and the length of treatment required for filarial infections in terms of patient compliance and reduced cost of treatment. Public Library of Science 2015-10-23 /pmc/articles/PMC4619673/ /pubmed/26496201 http://dx.doi.org/10.1371/journal.pntd.0004173 Text en © 2015 Binnebose et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Binnebose, Andrea M.
Haughney, Shannon L.
Martin, Richard
Imerman, Paula M.
Narasimhan, Balaji
Bellaire, Bryan H.
Polyanhydride Nanoparticle Delivery Platform Dramatically Enhances Killing of Filarial Worms
title Polyanhydride Nanoparticle Delivery Platform Dramatically Enhances Killing of Filarial Worms
title_full Polyanhydride Nanoparticle Delivery Platform Dramatically Enhances Killing of Filarial Worms
title_fullStr Polyanhydride Nanoparticle Delivery Platform Dramatically Enhances Killing of Filarial Worms
title_full_unstemmed Polyanhydride Nanoparticle Delivery Platform Dramatically Enhances Killing of Filarial Worms
title_short Polyanhydride Nanoparticle Delivery Platform Dramatically Enhances Killing of Filarial Worms
title_sort polyanhydride nanoparticle delivery platform dramatically enhances killing of filarial worms
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4619673/
https://www.ncbi.nlm.nih.gov/pubmed/26496201
http://dx.doi.org/10.1371/journal.pntd.0004173
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