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AAV vectors have become one of the leading platforms for gene therapy delivery. The inherent formation of empty AAV capsids during upstream production poses a challenge for drug developers, as empty AAV capsids lack the DNA payload and have no therapeutic benefit. Anion exchange chromatography (AEX) using membranes or resins has become a popular tool for the separation of empty and full capsids.
It is crucial that tools used to achieve empty/full AAV capsid separation provide effective, repeatable, and scalable separation. In many cases, the AEX operating space is narrow, and the reliability on processing equipment and reagents is critical. Therefore, having reproducible batches of AEX membranes or resins is necessary.
In this webinar, membrane reproducibility will be presented across three different manufacturing batches utilizing three different AAV5 feedstreams. Data will be shown demonstrating repeatability via rapidly cycling the membrane, which provides consistent performance and also opens up the possibility of reducing the size of the device at the manufacturing scale.
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