Size-exclusion chromatography as a multi-attribute method for process and product characterization of adeno-associated virus.

Mol Ther Methods Clin Dev

Process and Analytical Sciences, BioPharmaceuticals Development (BPD), R&D, AstraZeneca, Gaithersburg, MD, USA.

Published: December 2024

AI Article Synopsis

  • AAVs are becoming a key player in gene therapy, but their complex production requires thorough studies to ensure quality and consistency.
  • The study introduces a multiple-attribute monitoring (MAM) method that uses size-exclusion chromatography combined with various detectors to analyze important product quality attributes (PQAs) of AAVs simultaneously.
  • This new method is efficient, cost-effective, and showcases results comparable to traditional testing methods, making it a valuable tool for AAV product development and testing.

Article Abstract

Adeno-associated viruses (AAVs) have recently emerged as a leading platform for gene therapy. Due to the complex manufacturing process and structural features of AAVs, extensive process and product characterization studies are required to better understand product quality and batch-to-batch variability. It is, therefore, critical to develop a fast and reliable analytical method to monitor different product quality attributes (PQAs) of AAVs. In this study, we developed a multiple-attribute monitoring (MAM) method for the characterization of AAV PQAs. The MAM method was developed using the separation capability of size-exclusion chromatography (SEC) in connection with multiple in-line detectors: ultraviolet (UV), fluorescence (FLD), multi-angle light scattering (MALS), and refractive index (RI). We demonstrate that our SEC-based MAM method can be used to measure different PQAs, including genome and capsid titer, purity, aggregation, and full/empty capsid ratios in a single assay. Our SEC-based MAM method achieves similar results when compared side by side with orthogonal, individual assays such as quantitative polymerase chain reaction (qPCR), enzyme-linked immunosorbent assay (ELISA), and anion-exchange chromatography (AEX). Moreover, here we demonstrate that a simple, label-free, cost-effective, minimum sample requirement, and a high-throughput method can be applied to support process development, product characterization, release, and stability testing.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11647602PMC
http://dx.doi.org/10.1016/j.omtm.2024.101382DOI Listing

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