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作 者:王名强[1] 余黎[1] 安红[1] 崔焰[1] 韩平[1] 包红[1] 寇桂英[1] 周旭[2]
机构地区:[1]兰州生物制品研究所有限责任公司,兰州730046 [2]上海生物制品研究所有限责任公司,上海200052
出 处:《中国新药杂志》2012年第10期1166-1169,共4页Chinese Journal of New Drugs
基 金:国家科技支撑计划(2008BAI66B08)
摘 要:目的:对比荧光灶试验和TCID50-ELISA方法测定III价轮状病毒基因重配疫苗感染滴度的精确性,重复性和可行性。方法:同时采用TCID50-ELISA方法和荧光灶试验方法测定Ⅲ价轮状病毒基因重配疫苗的感染滴度,对测定结果进行比较分析。结果与结论:在Ⅲ价轮状病毒基因重配疫苗的感染滴度测定中,荧光灶试验方法和TCID50-ELISA方法各有其特点,荧光灶试验方法更加精确和快速,相对于TCID50-ELISA方法,具有更低的变异性,即其重复性较高;而TCID50-ELISA方法受主观因素的影响较低。Objective: To compare the accuracy, reproducibility, and applicability of fluorescent focus assay and TCID50-ELISA method for detecting infection titer of trivalent rotavirus reassortant vaccine. Methods: TCID50-ELISA method and fluorescent focus assay method were used to detect the infection titer of trivalent rotavirus reassortant vaccine. Test results were compared. Results and Conclusion: Each method for infectious titer of rota- virus has its own characteristics. Fluorescent focus assay is more accurate and faster than TCID50-ELISA method. Compared with TCID50-ELISA method, fluorescent focus assay has distinctly lower variance than TCID50-ELISA method, in other words, it has the finer reproducibility. Whereas the decision of mantissa by the fluorescent focus assay is more subjective than by TCID50-ELISA.
关 键 词:TCID50-ELISA 荧光灶试验 III价轮状病毒基因重配疫苗 感染滴度
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