Makra István, Terejánszky Péter, Gyurcsányi Róbert E
MTA-BME "Lendület" Chemical Nanosensors Research Group, Department of Inorganic and Analytical Chemistry, Budapest University of Technology and Economics, Szt. Gellért tér 4, Budapest 1111, Hungary.
MethodsX. 2015 Feb 16;2:91-9. doi: 10.1016/j.mex.2015.02.003. eCollection 2015.
Most often the determination of the concentration of virus particles is rendered difficult by the availability of proper standards. We have adapted a static light scattering based method for the quantification of virus particles (shown for poliovirus) without the need of virus particle standards. Instead, as standards, well-characterized polymeric nanoparticle solutions are used. The method is applicable for virus particles acting as Rayleigh scatterers, i.e., virus particles with equivalent diameters up to ca. 1/10th of the wavelength of the scattered monochromatic light (∼70 nm diameter). Further limitations may arise if the refractive index of the virus is unavailable or cannot be calculated based on its composition, such as in case of enveloped viruses. The method is especially relevant for preparation of virus particle concentration standards and to vaccine formulations based on attenuated or inactivated virus particles where the classical plaque forming assays cannot be applied. The method consists of: •Measuring the intensity of the light scattered by viruses suspended in an aqueous solution.•Measuring the intensity of the light scattered by polymeric nanoparticles of known concentration and comparable size with the investigated virus particle.•The concentration of virus nanoparticles can be calculated based on the two measured scattered light intensities by knowing the refractive index of the dispersing solution, of the polymer and virus nanoparticles as well as their relative sphere equivalent diameters.
大多数情况下,由于缺乏合适的标准品,病毒颗粒浓度的测定变得困难。我们采用了一种基于静态光散射的方法来定量病毒颗粒(以脊髓灰质炎病毒为例),无需病毒颗粒标准品。相反,使用特征明确的聚合物纳米颗粒溶液作为标准品。该方法适用于作为瑞利散射体的病毒颗粒,即等效直径高达散射单色光波长约1/10(直径约70 nm)的病毒颗粒。如果无法获得病毒的折射率或无法根据其组成计算折射率,如包膜病毒的情况,可能会出现进一步的限制。该方法对于制备病毒颗粒浓度标准品以及基于减毒或灭活病毒颗粒的疫苗制剂尤为重要,因为在这些情况下无法应用经典的蚀斑形成试验。该方法包括:•测量悬浮在水溶液中的病毒散射光的强度。•测量已知浓度且与所研究病毒颗粒尺寸相当的聚合物纳米颗粒散射光的强度。•通过了解分散溶液、聚合物和病毒纳米颗粒的折射率以及它们的相对球等效直径,基于两次测量的散射光强度计算病毒纳米颗粒的浓度。