Real-time monitoring of attenuated cytomegalovirus using Raman spectroscopy allows non-destructive characterization during flow.

IF 4.6
Shreya Milind Athalye, Murali K Maruthamuthu, Ehsan Esmaili, Miad Boodaghidizaji, Neelesh Sarathy, Cindy Mayorga, Jessica Raffaele, Vidhya Selvamani, Joseph P Smith, Tiago Matos, Richard R Rustandi, Arezoo M Ardekani, Mohit S Verma
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Abstract

Real-time monitoring of viral particles can have a crucial impact on vaccine manufacturing and can alleviate public health challenges by supporting continuous supply. Spectroscopic methods such as Raman spectroscopy can provide rapid and non-invasive measurements. Here, we have developed a Raman spectroscopy-based tool to monitor the quality and quantity of viral particles in a continuous flow setup. We characterized the attenuated human cytomegalovirus (CMV) across a wide range of concentrations (1.45 × 1010 to 2.90 × 1011 particles/mL) and flow rates (100 μm/s to 1000 μm/s) within a square quartz capillary. This process analytical technology (PAT) tool enables the detection of viral particles even at high flow rates such as 1000 μm/s. Sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) and dynamic light scattering (DLS) demonstrated that the samples maintain their integrity even after laser exposure, reiterating the non-invasive nature of Raman spectroscopy. To the best of our knowledge, this is the first report on characterizing CMV particles using Raman spectroscopy, especially under flow conditions. We have also demonstrated the limit of detection (LODmin) (2.01 × 1010 particles/mL) for CMV particles in continuous flow (1000 μm/s) (via the Raman spectroscopy method), addressing the effects of flow rate, concentration, and sample integrity. This technology could enable process control in the bio-manufacturing of vaccines.

利用拉曼光谱实时监测减毒巨细胞病毒,可以在流动过程中进行非破坏性表征。
对病毒颗粒的实时监测可对疫苗生产产生至关重要的影响,并可通过支持持续供应来缓解公共卫生挑战。光谱方法,如拉曼光谱可以提供快速和非侵入性的测量。在这里,我们开发了一种基于拉曼光谱的工具来监测病毒颗粒在连续流动设置中的质量和数量。我们在方形石英毛细管内对减毒的人巨细胞病毒(CMV)进行了广泛的浓度(1.45 × 1010至2.90 × 1011颗粒/mL)和流速(100 μm/s至1000 μm/s)的表征。该过程分析技术(PAT)工具即使在1000 μm/s的高流速下也能检测病毒颗粒。十二烷基硫酸钠-聚丙烯酰胺凝胶电泳(SDS-PAGE)和动态光散射(DLS)表明,即使在激光照射后,样品仍保持完整性,重申了拉曼光谱的非侵入性。据我们所知,这是第一个用拉曼光谱来表征CMV粒子的报告,特别是在流动条件下。我们还证明了CMV颗粒在连续流动(1000 μm/s)下(通过拉曼光谱方法)的检出限(LODmin) (2.01 × 1010颗粒/mL),解决了流速、浓度和样品完整性的影响。该技术可实现疫苗生物生产过程控制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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