Galue-Parra Adan Jesus, Jimenez-Falcao Sandra, Arribas-Yuste Esther, Marin Clotilde, Mendez-Arriaga Jose Manuel
Departamento de Parasitología, Universidad de Granada, Calle Severo Ochoa s/n, 18071 Granada, Spain.
Laboratory of Structural Biology, Institute of Biological Sciences, Federal University of Para, Belém 66075-110, PA, Brazil.
Biomedicines. 2025 Jul 6;13(7):1648. doi: 10.3390/biomedicines13071648.
Leishmaniasis remains a neglected tropical disease, with nearly one million new cases annually and limited investment in research. Current treatments, primarily based on pentavalent antimonials, are associated with severe side effects and increasing resistance. This study aims to develop a novel therapeutic strategy using a nanomaterial functionalized with sialic acid (SA) and colchicine (COL) to selectively target parasites. A nanostructured system was engineered by functionalizing its surface with SA and COL. SA was chosen to mimic host cell surfaces, enhancing parasite attraction, while COL was selected for its known leishmanicidal properties. The nanomaterial was designed to concentrate extracellular parasites on its surface via SA-mediated interactions, thereby increasing local COL efficacy. The functionalized nanomaterial demonstrated a dual mechanism: SA facilitated the selective accumulation of parasites on the nanostructure surface, while COL exerted a cytotoxic effect. This synergistic interaction resulted in enhanced parasite mortality in vitro, suggesting improved selectivity and potency compared to conventional treatments. The proposed nanomaterial offers a promising alternative for leishmaniasis treatment by combining targeted parasite attraction with localized drug delivery. This strategy may reduce systemic toxicity and improve therapeutic outcomes.
利什曼病仍然是一种被忽视的热带疾病,每年有近100万新病例,且研究投入有限。目前的治疗方法主要基于五价锑化合物,存在严重的副作用且耐药性不断增加。本研究旨在开发一种新的治疗策略,使用一种用唾液酸(SA)和秋水仙碱(COL)功能化的纳米材料来选择性靶向寄生虫。通过用SA和COL对其表面进行功能化设计构建了一种纳米结构系统。选择SA来模拟宿主细胞表面,增强对寄生虫的吸引力,而选择COL是因其已知的杀利什曼原虫特性。该纳米材料旨在通过SA介导的相互作用将细胞外寄生虫聚集在其表面,从而提高局部COL的疗效。功能化纳米材料表现出双重机制:SA促进寄生虫在纳米结构表面的选择性积累,而COL发挥细胞毒性作用。这种协同相互作用导致体外寄生虫死亡率提高,表明与传统治疗方法相比具有更高的选择性和效力。所提出的纳米材料通过将靶向寄生虫吸引与局部药物递送相结合,为利什曼病治疗提供了一种有前景的替代方法。这种策略可能会降低全身毒性并改善治疗效果。