Microfluidics enabled multi-omics triple-shot mass spectrometry for cell-based therapies

Author:

Slusher Gianna A.12ORCID,Kottke Peter A.2ORCID,Culberson Austin L.3ORCID,Chilmonczyk Mason A.3ORCID,Fedorov Andrei G.12ORCID

Affiliation:

1. Parker H. Petit Institute for Bioengineering and Bioscience, Georgia Institute of Technology 1 , Atlanta, Georgia 30332, USA

2. The George W. Woodruff School of Mechanical Engineering, Georgia Institute of Technology 2 , Atlanta, Georgia 30318, USA

3. Andson Biotech 3 , Atlanta, Georgia 30303, USA

Abstract

In recent years, cell-based therapies have transformed medical treatment. These therapies present a multitude of challenges associated with identifying the mechanism of action, developing accurate safety and potency assays, and achieving low-cost product manufacturing at scale. The complexity of the problem can be attributed to the intricate composition of the therapeutic products: living cells with complex biochemical compositions. Identifying and measuring critical quality attributes (CQAs) that impact therapy success is crucial for both the therapy development and its manufacturing. Unfortunately, current analytical methods and tools for identifying and measuring CQAs are limited in both scope and speed. This Perspective explores the potential for microfluidic-enabled mass spectrometry (MS) systems to comprehensively characterize CQAs for cell-based therapies, focusing on secretome, intracellular metabolome, and surfaceome biomarkers. Powerful microfluidic sampling and processing platforms have been recently presented for the secretome and intracellular metabolome, which could be implemented with MS for fast, locally sampled screening of the cell culture. However, surfaceome analysis remains limited by the lack of rapid isolation and enrichment methods. Developing innovative microfluidic approaches for surface marker analysis and integrating them with secretome and metabolome measurements using a common analytical platform hold the promise of enhancing our understanding of CQAs across all “omes,” potentially revolutionizing cell-based therapy development and manufacturing for improved efficacy and patient accessibility.

Funder

National Science FoundationCenter for Cell Manufacturing Technologies

Marcus Center for Therapeutic Cell Characterization and Manufacturing Collaboration Grant in Cell Manufacturing

Georgia Tech Foundation

Georgia Research Alliance

National Institute of General Medical Sciences

National Science Foundation

Publisher

AIP Publishing

Subject

Condensed Matter Physics,General Materials Science,Fluid Flow and Transfer Processes,Colloid and Surface Chemistry,Biomedical Engineering

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