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首页> 外文期刊>Analytical chemistry >Selective and Quantitative Detection of Influenza Virus Proteins in Commercial Vaccines Using Two-Dimensional High-Performance Liquid Chromatography and Fluorescence Detection
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Selective and Quantitative Detection of Influenza Virus Proteins in Commercial Vaccines Using Two-Dimensional High-Performance Liquid Chromatography and Fluorescence Detection

机译:二维高效液相色谱和荧光检测法选择性定量检测商业疫苗中的流感病毒蛋白

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In this work, we report on the applicability of two-dimensionalhigh-performance liquid chromatography (2D-HPLC) for the comprehensive characterization of inactivated influenza vaccine proteins. This novel procedure features minimal sample treatment and combines the on-line coupling of size exclusion HPLC to reversed-phase HPLC. A comparative analysis of commercial vaccines from three different manufacturers showed the method to be highly selective by providing characteristic reproducible chromatographic profiles for each vaccine. In addition, the method provided enhanced sensitivity for most constituents as a result of the use of native fluorescence detection in the reversed-phase HPLC step. The limits of detection (at a signal-to-noise ratio of >3) for hemagglutinin (HA) antigens were 105 and 172 ng/mL for influenza A/New Caledonia/20/99 and B/Jiangsu/10/2003 strains, respectively. The potential of this 2D-HPLC procedure in terms of quantitative antigen analysis was assessed by determination of the HA content of commercial vaccines. Results provided very good correlation with nominal HA values. The reproducibility (RSD) of the whole procedure was also evaluated and was found to be better than 2 and 3percent for calculated antigen concentrations expressed as micrograms of HA per milliliter in commercial vaccines for samples of the same lot (n velence 5) or different lots (n velence 3), respectively. In addition, it allowed the selective detection of several influenza constituents including nucleoproteins from type A and B viruses and the highly hydrophobic matrix protein 1 from both virus strains.
机译:在这项工作中,我们报告了二维高效液相色谱(2D-HPLC)对灭活流感疫苗蛋白的全面表征的适用性。这种新颖的程序具有最少的样品处理功能,并结合了体积排阻HPLC与反相HPLC的在线耦合。对来自三个不同制造商的商业疫苗进行的比较分析显示,该方法具有高度选择性,可为每种疫苗提供特征性的可重复色谱图。此外,由于在反相HPLC步骤中使用了天然荧光检测,该方法为大多数成分提供了更高的灵敏度。对于A型/新喀里多尼亚/ 20/99型和B / Jiangsu / 10/2003型流感病毒,血凝素(HA)抗原的检出限(信噪比> 3)为105和172 ng / mL,分别。通过确定商业疫苗的HA含量,可以评估2D-HPLC方法在定量抗原分析方面的潜力。结果提供了与标称HA值非常好的相关性。还评估了整个过程的可重复性(RSD),发现对于相同批次(nvelence 5)或不同批次的商业疫苗,计算出的抗原浓度表示为每毫升HA微克的计算抗原浓度优于2%和3%。 (n velence 3)。此外,它可以选择性检测几种流感成分,包括来自A型和B型病毒的核蛋白和来自两个病毒株的高度疏水性基质蛋白1。

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