End-to-End Biomanufacturing of Extracellular Vesicles

Extracellular vesicles (EVs) have emerged as next-generation, multispecific, and multifunctional agents across medicine, biotechnology, veterinary science, cosmetics, and nutrition. Their delivery efficiency of therapeutic cargo surpasses that of conventional carriers, and their capacity to simultaneously transport internal cargo and activate multiple recipient cells gives them a therapeutic versatility that no other platform can match. Translating this potential into real-world products depends on integrating process design with product characterization, a link that has not yet been systematically established for EV manufacturing. The functionality of an EV is inseparable from how it is made. EV composition is shaped at every stage of production, from the biology of the producer cell, to upstream microenvironmental stressors, to the operational parameters of downstream isolation and purification. Each of these variables influences the final product quality and functionality, which means that process design is, in effect, product design. While many guidelines, including minimal information for studies of extracellular vesicles (MISEV) and quality by design (QbD), have been reported, they operate at different levels: MISEV ensures the validity of EV characterization, whereas QbD defines how a manufacturer designs, controls, and releases a product. Currently, however, there is no link between them to provide an integrative framework. This manuscript, therefore reviews and proposes a framework for context-of-use-dependent EV biomanufacturing, in which biomanufacturing and bioprocessing parameters are deliberately matched to the intended application. By linking specific process conditions to resultant EV characteristics, and by fine-tuning upstream and downstream operations accordingly, bespoke EVs can be produced for defined therapeutic, diagnostic, or industrial purposes rather than made as a single generic product. Together, this work offers essential guidance for producing EVs at scale and for designing end-to-end bioprocesses that can be tailored to the diverse needs of future EV-based products.

Authors

Institutions

Publication Details

Journal
ACS Applied Materials & Interfaces
Published
2026-10-30
DOI
https://doi.org/10.1021/acsami.6c15984
Primary Topic
Extracellular vesicles in disease
Type
article
Field-Weighted Citation Impact
0.00

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

End-to-End Biomanufacturing of Extracellular Vesicles

Wojciech Chrzanowski, Emmanuelle Cameau, Qingyu Lei, Peter Guterstam et al.
1 links
ACS Applied Materials & Interfaces
Extracellular vesicles in disease
article

End-to-End Biomanufacturing of Extracellular Vesicles

Wojciech Chrzanowski, Emmanuelle Cameau, Qingyu Lei, Peter Guterstam, Daria Donati, Peiqing Zhang
article en

Abstract

Extracellular vesicles (EVs) have emerged as next-generation, multispecific, and multifunctional agents across medicine, biotechnology, veterinary science, cosmetics, and nutrition. Their delivery efficiency of therapeutic cargo surpasses that of conventional carriers, and their capacity to simultaneously transport internal cargo and activate multiple recipient cells gives them a therapeutic versatility that no other platform can match. Translating this potential into real-world products depends on integrating process design with product characterization, a link that has not yet been systematically established for EV manufacturing. The functionality of an EV is inseparable from how it is made. EV composition is shaped at every stage of production, from the biology of the producer cell, to upstream microenvironmental stressors, to the operational parameters of downstream isolation and purification. Each of these variables influences the final product quality and functionality, which means that process design is, in effect, product design. While many guidelines, including minimal information for studies of extracellular vesicles (MISEV) and quality by design (QbD), have been reported, they operate at different levels: MISEV ensures the validity of EV characterization, whereas QbD defines how a manufacturer designs, controls, and releases a product. Currently, however, there is no link between them to provide an integrative framework. This manuscript, therefore reviews and proposes a framework for context-of-use-dependent EV biomanufacturing, in which biomanufacturing and bioprocessing parameters are deliberately matched to the intended application. By linking specific process conditions to resultant EV characteristics, and by fine-tuning upstream and downstream operations accordingly, bespoke EVs can be produced for defined therapeutic, diagnostic, or industrial purposes rather than made as a single generic product. Together, this work offers essential guidance for producing EVs at scale and for designing end-to-end bioprocesses that can be tailored to the diverse needs of future EV-based products.

ACS Applied Materials & Interfaces
Uppsala University (SE), The University of Sydney (AU)
Wenner-Gren Stiftelserna, LEO Fondet, National Health and Medical Research Council
Good health and well-being
Openalex Percentile: Top 22%
Extracellular vesicles in disease
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.

Laika access coming soon