journal article·2024-08Open access

Gene Delivery From Granular Scaffolds for Tunable Biologics Manufacturing

Evan Kurt, Garth Devlin, Aravind Asokan, Tatiana Segura

Small· Volume 20· Issue 31

Abstract

Abstract The understanding of the molecular basis for disease has generated a myriad of therapeutic biologics, including therapeutic proteins, antibodies, and viruses. However, the promise that biologics can resolve currently incurable diseases hinges in their manufacturability. These therapeutics require that their genetic material be introduced to mammalian cells such that the cell machinery can manufacture the biological components. These are then purified, validated, and packaged. Most manufacturing uses batch processes that collect the biologic a few days following genetic modification, due to toxicity or difficulty in separating product from cells in a continuous operation, limiting the amount of biologic that can be produced and resulting in yearlong backlogs. Here, a scaffold‐based approach for continuous biologic manufacturing is presented, with sustained production of active antibodies and viruses for 30 days. The use of scaffold‐based biologic production enabled perfusion‐based bioreactors to be used, which can be incorporated into a fully continuous process.
Source: crossref · Quality: baseline

Research context

OpenAlex topics: CAR-T cell therapy research · Viral Infectious Diseases and Gene Expression in Insects · Virus-based gene therapy research

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Department of Biomedical Engineering Duke University Durham NC 27708 USA

Departments of Surgery and Molecular Genetics & Microbiology Duke University School of Medicine Durham NC 27710 USA

Departments Neurology and Dermatology Duke University Durham NC 27708 USA

Funding

National Institute of General Medical Sciences · National Institutes of Health

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