accelerating-in-vivo-car-t-development-using-single-nanoparticle-characterization
Accelerating In Vivo CAR-T Development Using Single Nanoparticle Characterization

Accelerating In Vivo CAR-T Development Using Single Nanoparticle Characterization

Panelists:

Image of Joseph Brealey

Joseph Brealey

Researcher
NanoFCM

Panelist

Image of Joseph Brealey

Joseph Brealey

Joseph Brealey has been a key member of NanoFCM’s research team for three years. With a background in biochemistry, Joseph focuses on the practical analysis of nanoparticles including extracellular vesicles (EVs), lipid nanoparticles (LNPs), and viral vectors, alongside development of novel analytical protocols.

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Broad clinical adoption of Chimeric Antigen Receptor (CAR) T cell therapies has been hindered by the complexity, cost, and toxicity of ex vivo manufacturing. Those factors are driving a shift toward in vivo CAR engineering using technologies like lipid nanoparticles (LNPs). However, efficient in vivo targeting remains challenging as LNPs generally accumulate in the liver/spleen, leading to modest transfection rates. Conjugating targeting proteins or antibodies to the surface of LNPs is one way to address this problem. And the single-molecule NanoAnalyzer technology from NanoFCM makes detecting and characterizing the particles in the payload—a necessary quality control step—a routine job.

In this GEN webinar, Joseph Brealey, an expert in nanoparticle delivery, will discuss current strategies for improving quality control of in vivo CAR T therapies. During the webinar, he will describe how NanoFCM’s single-molecule NanoAnalyzer sizes and counts LNPs label-free while detecting mRNA loading ratio, encapsulated mRNA, and surface-bound ligands/antibodies. You will learn how measurements such as mRNA copy number per particle, encapsulation efficiency, and antibody/ligand decoration levels can improve in vivo CAR T conversion efficiency.

A live Q&A session will follow the presentations, offering you a chance to pose questions to our expert panelist.

Produced with support from:

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