Article | June 6, 2025

Part One: Identifying Challenges In LVV Purification And Quantitation

By Poorni Adikaram, Ph.D., Tyler Frazier, and Timothy Fouts, Ph.D., CSO, at ABL Inc- . and Rebecca Montange, Ph.D, and Brandon Harrell at Sartorius

GettyImages-1256322400 lab

Growing demand for lentiviral vectors (LVVs) is creating the need for robust, scalable, GMP manufacturing processes. Accelerating process development can be difficult, however, due to a lack of rapid, reliable methods for LVV quantification. The Virus Counter® Plus platform (Sartorius) using the Virotag® VSVG assay enables quick (near-real-time) and precise determination of total particle counts and therefore supports rapid development of high-performing processes.

In this 3-part blog series, scientists from ABL, Inc. discuss the issues with current titer measurement methods, describe the Virus Counter Plus platform, and present highlights of a recent study conducted in collaboration with Sartorius to assess the correlation of titer data obtained using the new method to that generated using traditional physical and functional titer assays.

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