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Application of phage-indicator model in evaluation of antiviral drugs in vitro

机译:噬菌体指标模型在体外评估抗病毒药物评价中的应用

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A novel method which evaluates antiviral drugs in vitro by phage-indicator model was developed. The phage inactivation experiments were carried out with antiviral drugs of Shuanghuanglian (SHL), Ribavirin and Monoammonium Glycyrrizinate (MG). Firstly, the toxicity of three drugs to the indicator (E. coli) was determined to get rid of interference of the model system. The results indicated that SHL and Ribavirin had toxicity to the indicator, which was relative to their doses. The drug act of the three drugs was detected in the model. The data demonstrated that the phage survival was significantly inhibited by SHL and Ribavirin. After the interaction of the drugs and phage for 20 h, the inhibition rate of SHL and Ribavirin to phage survival reached the maximum of 89.69% and 47.50%, respectively, while MG had not any inhibition to phage. Based on these experimental results, evaluation of antiviral drug in vitro by means of the phageindicator model is feasible, practicable, and suitable for screening of antiviral drugs, especially for those from a large number of natural products isolated.
机译:开发了一种通过噬菌体指标模型在体外评估抗病毒药物的新方法。噬菌体灭活实验是用双黄连(SHL),利巴韦林和单烷烃(Mg)的抗病毒药物进行的。首先,确定三种药物对指标(大肠杆菌)的毒性被确定摆脱模型系统的干扰。结果表明,SHL和利巴韦林对指标具有相对于它们的剂量的毒性。在模型中检测到三种药物的药物作用。数据表明,SHL和利巴韦林显着抑制了噬菌体存活。药物和噬菌体相互作用20小时后,SHL和利巴韦林对噬菌体存活的抑制率分别达到89.69%和47.50%,而MG对噬菌体没有任何抑制。基于这些实验结果,通过噬菌体inder模型在体外评估抗病毒药物是可行的,切实可行的,并且适合筛选抗病毒药物,特别是对于来自分离的大量天然产物的抗病毒药物。

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