In Vitro Stability of the Biological Activity of Voriconazole against Acanthamoeba castellanii

Barbara Czerniak Rodrigues, M. Büchele, Carolina de Jesus de Camargo, F. Filippin-Monteiro, K. Caumo
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Abstract

Acanthamoeba keratitis (AK) is a rare cornea disease caused by species of the Acanthamoeba genus. The antifungal voriconazole blocks the ergosterol synthesis in the protozoan membrane and is active against the cysts and trophozoites of Acanthamoeba spp. Due to the low stability of voriconazole, its options for eye drops are scarce. This study aimed to investigate the stability of the biological activity of voriconazole against two strains of Acanthamoeba castellanii and one clinical isolate from a patient with AK. To evaluate the stability of the biological activity of voriconazole, strains of A. castellanii (ATCC 50492) were exposed to different periods and voriconazole concentrations stored at 4 °C for 7, 15, and 30 days. The cytotoxicity assays were performed using SIRC (ATCC CCL-60™) cell line. The results indicated the amoebicidal effect of voriconazole against Acanthamoeba spp. within 24 h and 48 h of exposure, and the voriconazole solution was stable and retained antiamoebic activity when stored at 4 °C for up to 30 days. In the cytotoxicity test, the result demonstrated low cytotoxicity of the drug to the corneal rabbit cell line. However, there is a need to carry out further synergistic effects with other antiamoebic drugs and then in vivo experiments in the AK animal model.
伏立康唑抗棘阿米巴生物活性的体外稳定性
棘阿米巴角膜炎(AK)是一种由棘阿米巴属引起的罕见角膜疾病。抗真菌伏立康唑阻断原生动物膜中麦角甾醇的合成,对棘阿米巴的囊肿和滋养体具有活性。由于伏立康唑的稳定性低,其滴眼液的选择很少。本研究旨在研究伏立康唑对两株棘阿米巴和一名AK患者临床分离株的生物活性的稳定性。为了评估伏立康唑生物活性的稳定性,将A.castellanii菌株(ATCC 50492)暴露于不同时期和伏立康唑浓度下,在4°C下储存7、15和30天。使用SIRC(ATCC CCL-60™) 细胞系。结果表明,伏立康唑在暴露24小时和48小时内对棘阿米巴具有杀阿米巴作用。伏立康唑溶液在4°C下储存30天时稳定并保持抗阿米巴活性。在细胞毒性试验中,结果表明该药物对角膜兔细胞系的细胞毒性较低。然而,需要与其他抗阿米巴药物进行进一步的协同作用,然后在AK动物模型中进行体内实验。
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CiteScore
1.70
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