Microfluidic Synthesis of Scalable Layer-by-Layer Multiple Antigen Nano-Delivery Platform for SARS-CoV-2 Vaccines.
Yang XuKazuya MasudaChristine GrosoRick HassanZiyou ZhouKelsey BroderickMoriya TsujiChristopher TisonPublished in: Vaccines (2024)
The COVID-19 outbreak was a global pandemic with wide-ranging healthcare implications. Although several mRNA-based vaccines delivered using lipid nanoparticles (LNP) have been approved and demonstrated efficacy at reducing the severity and spread of infection, continued rapid viral evolution and disadvantages currently associated with LNP delivery vehicles (such as toxicity) are driving the design of next-generation SARS-CoV-2 vaccines. Herein, we describe the development of a trimethylated chitosan-based nanoparticle layer-by-layer (LbL) delivery platform for multiple antigens as a scalable and safe COVID-19 vaccine, known as, "LbL-CoV19". These vaccine candidates have been demonstrated to be biocompatible, safe, and effective at stimulating both humoral and cellular responses for protection in preclinical studies. Preliminary results also indicate that LbL-CoV19 can potentially achieve rapid, long-lasting, and broad protection against the SARS-CoV-2 challenge. The "plug-and-play" platform technology is well suited to preparedness for future pandemics and disease outbreaks.
Keyphrases
- sars cov
- respiratory syndrome coronavirus
- high throughput
- healthcare
- immune response
- public health
- drug delivery
- coronavirus disease
- single cell
- stem cells
- dendritic cells
- oxidative stress
- loop mediated isothermal amplification
- mesenchymal stem cells
- infectious diseases
- hyaluronic acid
- cell therapy
- quantum dots
- label free