Abstract
Schistosomiasis, a parasitic disease affecting around 250 million people globally, primarily children, necessitates the urgent development of pediatric praziquantel formulations, as outlined in the WHO neglected tropical diseases roadmap 2021-2030. We developed a low-cost PZQ nanoformulation utilizing a self-nanoemulsified delivery system (SNEDDS-PZQ). Physicochemical characterization confirms its hydrodynamic size and suitability for semi-industrial pilot batch production. Toxicity studies across multiple models demonstrate its safety profile. In vivo studies in schistosomiasis animal models reveal significant parasite load reduction (over 95%) with a single oral dose of 200 and 400 mg/kg of SNEDDS-PZQ, surpassing free praziquantel efficacy. Pharmacokinetic analyses demonstrate increased PZQ blood levels postadministration of SNEDDS-PZQ. Our findings highlight the promise of this innovative approach in pediatric schistosomiasis treatment by using this nanotechnology as a delivery system, offering potential for widespread application.
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Mengarda, A. C., Iles, B., Rodrigues, V. C., Lima, A. L., Machado, V. P., Reatgui, W. S., … de Moraes, J. (2025). Praziquantel Nanoparticle Formulation for the Treatment of Schistosomiasis. ACS Applied Nano Materials, 8(8), 3985–3997. https://doi.org/10.1021/acsanm.4c06757
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