Cemal Shaul D, Ladetto María F, Alava Katherine Hermida, Kazimirsky Gila, Cucher Marcela, Glisoni Romina J, Cuestas María L, Byk Gerardo
Department of Chemistry, Bar-Ilan University, Ramat Gan 5290002, Israel.
Instituto de Investigaciones en Microbiología y Parasitología Médica (IMPaM), CONICET, Universidad de Buenos Aires, Buenos Aires 1121, Argentina.
Pharmaceutics. 2025 May 30;17(6):725. doi: 10.3390/pharmaceutics17060725.
: Filamentous fungi, in particular the species , , and , frequently colonize the lungs of cystic fibrosis (CF) patients. Chronic colonization is linked to hypersensitivity reactions and persistent infections leading to a significant long-term decline in lung function. Azole antifungal therapy such as voriconazole (VRC) slows disease progression, particularly in patients with advanced CF; however, excessive mucus production in CF lungs poses a diffusional barrier to effective treatment. : Here, biodegradable nanohydrogels (NHGs) recently developed as nanocarriers were evaluated for formulating VRC as a platform for treating fungal infections in CF lungs. The NHGs entrapped up to about 30 μg/mg of VRC, and physicochemical properties were investigated via dynamic laser light scattering and nanoparticle tracking analysis. Diameters were 100-400 nm, and excellent colloidal stability was demonstrated in interstitial fluids, indicating potential for pulmonary delivery. Nano-formulations exhibited high in vitro cytocompatibility in A549 and HEK293T cells and were tested for the release of VRC under two different sink conditions. : Notably, the antifungal activity of VRC-loaded nanohydrogels was up to eight-fold greater than an aqueous suspension drug against different fungal species isolated from CF sputum, regardless of the presence of a CF artificial mucus layer. : These findings support the development of potent VRC nano-formulations for treating fungal disorders in CF lungs.
丝状真菌,尤其是 、 和 等物种,经常在囊性纤维化(CF)患者的肺部定植。慢性定植与超敏反应和持续性感染有关,导致肺功能长期显著下降。伏立康唑(VRC)等唑类抗真菌疗法可减缓疾病进展,尤其是在晚期CF患者中;然而,CF肺部过多的黏液分泌对有效治疗构成了扩散障碍。在此,对最近开发的作为纳米载体的可生物降解纳米水凝胶(NHGs)进行了评估,以将VRC配制成治疗CF肺部真菌感染的平台。NHGs可包封高达约30μg/mg的VRC,并通过动态激光散射和纳米颗粒跟踪分析研究其物理化学性质。直径为100 - 400nm,在间质液中表现出优异的胶体稳定性,表明具有肺部给药的潜力。纳米制剂在A549和HEK293T细胞中表现出高体外细胞相容性,并在两种不同的漏槽条件下测试了VRC的释放。值得注意的是,负载VRC的纳米水凝胶对从CF痰液中分离出的不同真菌物种的抗真菌活性比水悬浮药物高八倍,无论是否存在CF人工黏液层。这些发现支持开发有效的VRC纳米制剂用于治疗CF肺部的真菌疾病。