Adsorption and intercalation of benznidazole and nifurtimox in montmorillonite: An experimental-theoretical study
American trypanosomiasis or Chagas disease, caused by Trypanosoma cruzi , remains a therapeutic challenge worldwide. Benznidazole (BNZ) and Nifurtimox (NFX) are drugs used for its treatment; however, they are not efficacy in the chronic phase of the disease, which leads to high toxicity due to prolo...
| Autores: | , , , , , , , , , , , |
|---|---|
| Tipo de recurso: | artículo |
| Estado: | Versión publicada |
| Fecha de publicación: | 2026 |
| País: | España |
| Institución: | Consejo Superior de Investigaciones Científicas (CSIC) |
| Repositorio: | DIGITAL.CSIC. Repositorio Institucional del CSIC |
| OAI Identifier: | oai:digital.csic.es:10261/417506 |
| Acceso en línea: | http://hdl.handle.net/10261/417506 https://doi.org/10.1016/j.clay.2026.108142 |
| Access Level: | acceso abierto |
| Palabra clave: | Trypanosoma cruzi Benznidazole Nifurtimox Clay-drug nanocomplexes High toxicity Molecular modeling Clay minerals DFT calculations Intercalation |
| Sumario: | American trypanosomiasis or Chagas disease, caused by Trypanosoma cruzi , remains a therapeutic challenge worldwide. Benznidazole (BNZ) and Nifurtimox (NFX) are drugs used for its treatment; however, they are not efficacy in the chronic phase of the disease, which leads to high toxicity due to prolonged use. This research addresses the use of nanomaterials (Nano clay and VHS) as natural systems capable of adsorbing drugs with low water solubility, allowing improved release to reduce adverse effects. The objectives were to study the crystal structures of NFX and BNZ at the atomic scale, using quantum mechanics calculations and experimental techniques (XRD, FTIR, TGA, SEM-EDS), to understand their physicochemical characteristics in the crystalline state, as well as to explore their hydration by molecular dynamics simulations. The intercalation of these drugs in the confined space between the montmorillonite layers was evaluated by DFT calculations to propose novel clay-drug nanocomplexes for enhancing the solubility and bioavailability. The results showed that NFX intercalation in both clays presented a loss of crystallinity, with a displacement of the (001) plane, while BNZ exhibited slight intercalation being adsorbed mainly on the external surfaces of clay mineral solids. Montmorillonite enhanced the stability of these drugs through interactions (hydrogen bonding, electrostatic interactions, and coordination with Na+ cations), adopting parallel orientations with the clay layers. The intercalation of NFX and BNZ into the interlaminar space of montmorillonite was energetically favorable. The design of clay-drug nanocomplexes could be a potential alternative for developing new, more effective and safer therapeutic schemes against Chagas disease. |
|---|