锌(II)-2,4,5-三苯基-1H-咪唑配合物对Vero细胞复制DENV-2的影响

T. H. Sucipto, A. Wibrianto, F. Martak, Siti Churrotin, I. H. Amarullah, H. Setyawati, Puspa Wardhani, A. Aryati, S. Soegijanto
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摘要

登革热病毒(DENV)是世界范围内出现的一种重要病原体,是传染病的病因。登革热病毒通过埃及伊蚊和白纹伊蚊的雌性蚊子传播给人类。印度尼西亚是世界上登革热流行地区最大的国家之一。登革热于1968年首次在泗水和雅加达暴发。为预防和治疗DENV感染已作出许多努力,目前正在对若干疫苗进行临床试验。DENV的抗病毒测试是药物表征和开发的重要替代方法。金属和有机的络合反应形成了络合化合物。复合化合物可作为抗炎、抗菌、抗真菌、抗菌、抗病毒。Zn2+离子可作为抗病毒候选物。本课题的目的是研究锌(II)-2,4,5-三苯基- 1h -咪唑抗病毒化合物在细胞培养中对DENV-2复制的抑制作用。采用抗病毒活性试验和细胞毒性试验检测DENV复制。采用病毒ToxGloTM法测定锌(II)-2,4,5-三苯基- 1h -咪唑配合物的抑制活性。采用CellTiter96®AQuoeus法测定锌(II)-2,4,5-三苯基- 1h -咪唑配合物的细胞毒性。锌(II)-2,4,5-三苯基- 1h -咪唑对2型登革热病毒的抑制浓度(IC50)为34.42 μg/ml。化合物对Vero细胞的细胞毒浓度(CC50) <100 μg/ml。本研究结果证实了锌(II)-2,4,5-三苯基- 1h -咪唑配合物对血清2型登革热的抑制作用及其对Vero细胞的高毒性。锌(II)-2,4,5-三苯基咪唑是否可用于治疗DENV-2感染尚不需要进一步的研究
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Effect of Zinc(II)-2,4,5-triphenyl-1H-imidazole Complex Against Replication DENV-2 in Vero Cell
Dengue virus (DENV) is a significant pathogen emerging worldwide as a cause of infectious disease. DENVs are transmitted to humans through female mosquitoes from Aedes aegypti and Aedes albopictus species. Indonesia is one of the largest countries in the world in dengue endemic regions worldwide. Dengue fever was occurred for the first time as an outbreak in Surabaya and Jakarta in 1968. Many efforts have been made to prevent and treat DENV infections, and clinical trials of a number of vaccines are currently underway. Antiviral testing of DENV is an important alternative for drug characterization and development. Complex compounds are formed as a result of metal and organic complex reactions. Complex compounds can be used as an anti-inflammatory, antimicrobial antifungal, antibacterial, antivirus. The Zn2+ ion can be used as an antiviral candidate. The purpose of this project was investigated Zinc(II)-2,4,5-triphenyl-1H-imidazole antiviral compound to be further tested for inhibitory effect on the replication of DENV-2 in cell culture. DENV replication was measured by antiviral activity assay and cytotoxicity assay. The inhibitory activity of Zinc(II)-2,4,5-triphenyl-1H-imidazole complex compound was determined by Viral ToxGloTM Assay. The cytotoxicity of Zinc(II)-2,4,5-triphenyl-1H-imidazole complex compound was determined by CellTiter96® AQuoeus assay. The inhibitory concentration (IC50) of Zinc(II)-2,4,5-triphenyl- 1H-imidazole against dengue virus type-2 was 34.42 μg/ml. The cytotoxic concentration (CC50) of compound against Vero cell was <100 μg/ml. The results of this study demonstrate the antidengue serotype 2 inhibitory activity of investigated Zinc(II)-2,4,5-triphenyl-1H-imidazole complex and its high toxicity in Vero cells. Further studies are not required before investigated Zinc(II)-2,4,5-triphenylimidazole can be applied in the treatment of DENV-2 infections
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