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Biophysical Characterization of Adeno-Associated Virus Vectors Using Ion-Exchange Chromatography Coupled to Light Scattering Detectors
Authors:Christina Wagner  Bernd Innthaler  Martin Lemmerer  Robert Pletzenauer  Ruth Birner-Gruenberger
Affiliation:1.Analytical Development Europe, Takeda Vienna, 1220 Vienna, Austria;2.Gene Therapy Process Development, Takeda Orth an der Donau, 2304 Orth an der Donau, Austria;3.Institute of Chemical Technologies and Analytics, Technische Universität Wien, 1060 Vienna, Austria
Abstract:Ion-exchange chromatography coupled to light scattering detectors represents a fast and simple analytical method for the assessment of multiple critical quality attributes (CQA) in one single measurement. The determination of CQAs play a crucial role in Adeno-Associated Virus (AAV)-based gene therapies and their applications in humans. Today, several different analytical techniques, including size-exclusion chromatography (SEC), analytical ultracentrifugation (AUC), qPCR or ELISA, are commonly used to characterize the gene therapy product regarding capsid titer, packaging efficiency, vector genome integrity, aggregation content and other process-related impurities. However, no universal method for the simultaneous determination of multiple CQAs is currently available. Here, we present a novel robust ion-exchange chromatography method coupled to multi-angle light scattering detectors (IEC-MALS) for the comprehensive characterization of empty and filled AAVs concerning capsid titer, full-to-total ratio, absolute molar mass of the protein and nucleic acid, and the size and polydispersity without baseline-separation of both species prior to data analysis. We demonstrate that the developed IEC-MALS assay is applicable to different serotypes and can be used as an orthogonal method to other established analytical techniques.
Keywords:adeno-associated virus vectors   ion-exchange chromatography   multi-angle light scattering   dynamic light scattering   protein characterization   critical quality attributes
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