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Evaluation of electrospray differential mobility analysis for virus particle analysis: Potential applications for biomanufacturing

机译:用于病毒颗粒分析的电喷雾差分迁移率分析评估:生物制造的潜在应用

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摘要

The technique of electrospray differential mobility analysis (ES-DMA) was examined as a potential potency assay for routine virus particle analysis in biomanufacturing environments (e.g., evaluation of vaccines and gene delivery products for lot release) in the context of the International Committee of Harmonisation (ICH) Q2 guidelines. ES-DMA is a rapid particle sizing method capable of characterizing certain aspects of the structure (such as capsid proteins) and obtaining complete size distributions of viruses and virus-like particles. It was shown that ES-DMA can distinguish intact virus particles from degraded particles and measure the concentration of virus particles when calibrated with nanoparticles of known concentration. The technique has a measurement uncertainty of ≈20%, is linear over nearly 3 orders of magnitude, and has a lower limit of detection of ≈10  particles/mL. This quantitative assay was demonstrated for non-enveloped viruses. It is expected that ES-DMA will be a useful method for applications involving production and quality control of vaccines and gene therapy vectors for human use.
机译:在国际协调委员会的背景下,对电喷雾差分迁移分析技术(ES-DMA)进行了检查,以作为生物生产环境中常规病毒颗粒分析的潜在效价分析方法(例如,评估疫苗和用于批量释放的基因递送产品) (ICH)第二季度指南。 ES-DMA是一种快速的粒度分析方法,能够表征结构的某些方面(例如衣壳蛋白)并获得病毒和病毒样颗粒的完整尺寸分布。结果表明,当用已知浓度的纳米粒子进行校准时,ES-DMA可以区分完整的病毒粒子和降解的粒子,并测量病毒粒子的浓度。该技术的测量不确定度为≈20%,在近3个数量级上呈线性,检测下限为≈10个颗粒/ mL。对于非包膜病毒证明了该定量测定。预期ES-DMA将成为涉及人用疫苗和基因治疗载体的生产和质量控制的应用的有用方法。

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