Accéder au contenu
Merck

Polyanhydride Nanoparticle Delivery Platform Dramatically Enhances Killing of Filarial Worms.

PLoS neglected tropical diseases (2015-10-27)
Andrea M Binnebose, Shannon L Haughney, Richard Martin, Paula M Imerman, Balaji Narasimhan, Bryan H Bellaire
RÉSUMÉ

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.

MATÉRIAUX
Référence du produit
Marque
Description du produit

Sigma-Aldrich
Diméthylsulfoxyde, Hybri-Max, sterile-filtered, BioReagent, suitable for hybridoma, ≥99.7%
Sigma-Aldrich
Acétone, ACS reagent, ≥99.5%
Sigma-Aldrich
Diméthylsulfoxyde, ACS reagent, ≥99.9%
Sigma-Aldrich
Diméthylsulfoxyde, for molecular biology
Sigma-Aldrich
Acide sulfurique, ACS reagent, 95.0-98.0%
Sigma-Aldrich
Acide acétique, glacial, ACS reagent, ≥99.7%
Sigma-Aldrich
N,N-Diméthylformamide, ACS reagent, ≥99.8%
Sigma-Aldrich
Diméthylsulfoxyde, sterile-filtered, BioPerformance Certified, meets EP, USP testing specifications, suitable for hybridoma
Sigma-Aldrich
Hydroxyde de sodium, ACS reagent, ≥97.0%, pellets
Sigma-Aldrich
Acide acétique, glacial, ReagentPlus®, ≥99%
Sigma-Aldrich
Chloroforme, contains 100-200 ppm amylenes as stabilizer, ≥99.5%
Sigma-Aldrich
Hydroxyde de sodium, reagent grade, ≥98%, pellets (anhydrous)
Sigma-Aldrich
Toluène, ACS reagent, ≥99.5%
Sigma-Aldrich
Diméthylsulfoxyde, ReagentPlus®, ≥99.5%
Sigma-Aldrich
Éther diéthylique, anhydrous, ACS reagent, ≥99.0%, contains BHT as inhibitor
Sigma-Aldrich
1-Méthyl-2-pyrrolidinone, ACS reagent, ≥99.0%
Sigma-Aldrich
Hydroxyde de sodium solution, 50% in H2O
Sigma-Aldrich
Potassium carbonate, ACS reagent, ≥99.0%
Sigma-Aldrich
Éther diéthylique, ACS reagent, anhydrous, ≥99.0%, contains BHT as inhibitor
Sigma-Aldrich
1-Méthyl-2-pyrrolidinone, ReagentPlus®, 99%
Sigma-Aldrich
Diméthylsulfoxyde, ≥99.5% (GC), suitable for plant cell culture
Sigma-Aldrich
Chloroforme, contains ethanol as stabilizer, ACS reagent, ≥99.8%
Sigma-Aldrich
Acétonitrile, ACS reagent, ≥99.5%
Sigma-Aldrich
DAPI, for nucleic acid staining
Sigma-Aldrich
Hydroxyde de sodium solution, BioUltra, for molecular biology, 10 M in H2O
Sigma-Aldrich
Acide acétique, glacial, ≥99.99% trace metals basis
Sigma-Aldrich
Acide sulfurique, 99.999%
Sigma-Aldrich
Pentane, ≥99% (GC)
Sigma-Aldrich
Hydroxyde de sodium, BioXtra, ≥98% (acidimetric), pellets (anhydrous)
Sigma-Aldrich
N,N-Diméthylacétamide, ReagentPlus®, 99%