Abstract

Adeno associated virus (AAV) capsids are a leading modality for in vivo gene delivery. Complete and precise characterization of capsid particles, including capsid and vector genome concentration, is necessary to safely and efficaciously dose patients. Size exclusion chromatography (SEC) coupled to multiangle light scattering (MALS) offers a straightforward approach to comprehensively characterize AAV capsids. The current study demonstrates that this method provides detailed AAV characterization information, including but not limited to aggregation profile, size-distribution, capsid content, capsid molar mass, encapsidated DNA molar mass, and total capsid and vector genome titer. Currently, multiple techniques are required to generate this information, with varying accuracy and precision. In the current study, a new series of equations for SEC-MALS are used in tandem with intrinsic properties of the capsids and encapsidated DNA to quantify multiple physical AAV attributes in one 20-min run with minimal sample manipulation, high accuracy, and high precision. These novel applications designate this well-established method as a powerful tool for product development and process analytics in future gene therapy programs.

Details

Title
Comprehensive characterization and quantification of adeno associated vectors by size exclusion chromatography and multi angle light scattering
Author
McIntosh, Nicole L. 1 ; Berguig, Geoffrey Y. 1 ; Karim, Omair A. 1 ; Cortesio, Christa L. 1 ; De Angelis, Rolando 1 ; Khan, Ayesha A. 1 ; Gold, Daniel 1 ; Maga, John A. 1 ; Bhat, Vikas S. 1 

 BioMarin Pharmaceutical, Inc., Novato, USA (GRID:grid.422932.c) (ISNI:0000 0004 0507 5335) 
Publication year
2021
Publication date
2021
Publisher
Nature Publishing Group
e-ISSN
20452322
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
2736949804
Copyright
© The Author(s) 2021. corrected publication 2022. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.