Proteins‐Based Nanoparticles for Benznidazole Enteric Delivery

Chagas disease, caused by Trypanosoma cruzi (T. cruzi), affects millions worldwide, particularly in Latin America. Despite its prevalence, treatment options remain limited. Current drugs, such as benznidazole, cause adverse effects possibly due to ineffective administration. In this context, nanoparticles offer a promising solution to target and control drug delivery by leading the effector site and minimizing side effects. This article focuses on zein-casein-based nanoparticles (Bioparticles, BP) coated with Eudragit L100-55 (BP:EU) for enteric delivery of benznidazole. BP:EU structures are synthesized to minimize premature drug release in the stomach, promoting release in the small intestine. Physical characterization confirmed the successful synthesis of BP:EU and their pH-responsive trigger for drug release. These findings suggest that this material can be a promising approach for Chagas disease treatment, addressing challenges in benznidazole delivery that can lead to improved therapeutic responses.

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Publication Details

Journal
Macromolecular Bioscience
Published
2024-10-18
DOI
https://doi.org/10.1002/mabi.202400338
Citations
2
Primary Topic
Trypanosoma species research and implications
Type
article
Field-Weighted Citation Impact
0.77

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article

Proteins‐Based Nanoparticles for Benznidazole Enteric Delivery

Roque J. Minari, Ana S. Sonzogni, Mariana Allasia, Verónica Gonzalez et al.
2 citations
Macromolecular Bioscience
Trypanosoma species research and implications
0.77
article

Proteins‐Based Nanoparticles for Benznidazole Enteric Delivery

Roque J. Minari, Ana S. Sonzogni, Mariana Allasia, Verónica Gonzalez, Victor A. Pilicita, Florencia Borra
article en
2 citations

Abstract

Chagas disease, caused by Trypanosoma cruzi (T. cruzi), affects millions worldwide, particularly in Latin America. Despite its prevalence, treatment options remain limited. Current drugs, such as benznidazole, cause adverse effects possibly due to ineffective administration. In this context, nanoparticles offer a promising solution to target and control drug delivery by leading the effector site and minimizing side effects. This article focuses on zein-casein-based nanoparticles (Bioparticles, BP) coated with Eudragit L100-55 (BP:EU) for enteric delivery of benznidazole. BP:EU structures are synthesized to minimize premature drug release in the stomach, promoting release in the small intestine. Physical characterization confirmed the successful synthesis of BP:EU and their pH-responsive trigger for drug release. These findings suggest that this material can be a promising approach for Chagas disease treatment, addressing challenges in benznidazole delivery that can lead to improved therapeutic responses.

Macromolecular BioscienceVol. 25(1)
Consejo Nacional de Investigaciones Científicas y Técnicas (AR), Universidad Nacional del Litoral (AR), Instituto de Desarrollo Tecnológico para la Industria Química (AR)
Consejo Nacional de Investigaciones Científicas y Técnicas, Universidad Nacional del Litoral, Agencia Nacional de Promoción de la Investigación, el Desarrollo Tecnológico y la Innovación
Good health and well-being
Openalex Percentile: Top 25%
Trypanosoma species research and implications
0.77
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Proteins‐Based Nanoparticles for Benznidazole Enteric Delivery — Roque J. Minari, Ana S. Sonzogni, et al. · Macromolecular Bioscience (2024) | TGRS Research Map | TGRS