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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:提出了一种新的通过噬菌体指标模型评价抗病毒药物的方法。用双黄连(SHL),利巴韦林和甘草酸单铵(MG)的抗病毒药物进行噬菌体灭活实验。首先,确定三种药物对指示剂(大肠杆菌)的毒性,以摆脱模型系统的干扰。结果表明,SHL和利巴韦林对指示剂具有毒性,这是相对于其剂量而言的。在模型中检测到这三种药物的药物行为。数据表明,SHL和利巴韦林显着抑制了噬菌体的存活。药物与噬菌体相互作用20 h后,SHL和利巴韦林对噬菌体存活的抑制率分别达到最大,分别为89.69%和47.50%,而MG对噬菌体没有任何抑制作用。基于这些实验结果,通过噬菌体指示剂模型体外评价抗病毒药物是可行,可行的,并且适合于抗病毒药物的筛选,特别是对于来自大量天然产物的抗病毒药物的筛选。

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