Lipid nanoparticles (LNPs) have enormous potential for the delivery of genomic medicine. One obstacle, however, is the lack of effective ways to target specific cell types. In order to target lung cells, the identification of chemically distinct lipid libraries would first be necessary.
Now, a team of engineers at the University of Pennsylvania led by Michael Mitchell, PhD, associate professor in the department of bioengineering, has developed a new means of targeting the lungs with LNPs. More specifically, they report the implementation “of a barcoded high-throughput screening system as a means to identify the lung-targeting efficacy of cationic, degradable lipid-like materials.”
The findings demonstrate a new method for efficiently determining which LNPs are likely to bind to the lungs, rather than the liver. “The way the liver is designed,” said Mitchell, “LNPs tend to filter into hepatic cells, and struggle to arrive anywhere else. Being able to target the lungs is potentially life-changing for someone with lung cancer or cystic fibrosis.”
This is published in Nature Communications in the paper, “High-throughput barcoding of nanoparticles identifies cationic, degradable lipid-like materials for mRNA delivery to the lungs in female preclinical models.”
Previous studies have shown that cationic lipids are more likely to successfully deliver their contents to lung tissue. “However, the commercial cationic lipids are usually highly positively charged and toxic,” said Lulu Xue, PhD, a postdoctoral fellow in the Mitchell Lab.
Typically, it would require hundreds of mice to individually test the members of a library of LNPs to find one with a low charge that has a higher likelihood of delivering a medicinal payload to the lungs.
Instead, the team used barcoded DNA to tag each LNP with a unique strand of genetic material. More specifically, they combinatorially synthesized 180 cationic, degradable lipids. Then, they used barcoding technology to quantify how the selected 96 distinct lipid nanoparticles deliver DNA barcodes in vivo.
After identifying an LNP that successfully penetrated lung cells—the top-performing nanoparticle formulation delivering Cas9-based genetic editors—they were administered to a lung tumor model in female mice.
The treatment had a positive effect, drastically reducing tumor size by delivering a strand of mRNA and gRNA that suppresses the growth of lung tumors. “This technology will help to accelerate the development of mRNA therapeutics beyond the liver,” said Xue, pointing to the speed, low cost, and efficacy of the technique.
The authors wrote that the data demonstrate that “employing high-throughput barcoding technology as a screening tool for identifying nanoparticles with lung tropism holds potential for the development of next-generation extrahepatic delivery platforms.”
https://www.genengnews.com/topics/drug-discovery/lipid-nanoparticles-engineered-to-target-lung-cells-reduce-tumor-size-in-mice/
Check out our mRNA service to expedite your vaccine research
PackGene Biotech is a world-leading CRO and CDMO, excelling in AAV vectors, mRNA, plasmid DNA, and lentiviral vector solutions. Our comprehensive offerings span from vector design and construction to AAV, lentivirus, and mRNA services. With a sharp focus on early-stage drug discovery, preclinical development, and cell and gene therapy trials, we deliver cost-effective, dependable, and scalable production solutions. Leveraging our groundbreaking π-alpha 293 AAV high-yield platform, we amplify AAV production by up to 10-fold, yielding up to 1e+17vg per batch to meet diverse commercial and clinical project needs. Moreover, our tailored mRNA and LNP products and services cater to every stage of drug and vaccine development, from research to GMP production, providing a seamless, end-to-end solution.
Related News
Sangamo Therapeutics Secures Accelerated Approval Pathway for Gene Therapy in Fabry Disease
Sangamo Therapeutics has announced a major advancement in its gene therapy program for Fabry disease, as the U.S. FDA has provided a clear pathway for Accelerated Approval. This decision could potentially speed up approval timelines by three years, with a Biologics...
[2024/10/18] Gene and Cell Therapy- weekly digest from PackGene
FeaturedNewsArticlesPackGene's NewsletterReceive the latest news and insights to your inbox.About PackGenePackGene Biotech is a world-leading CRO and CDMO, excelling in AAV vectors, mRNA, plasmid DNA, and lentiviral vector solutions. Our comprehensive offerings span...
GSK sues Moderna over mRNA vaccine patents, seeks ‘reasonable royalty’
GSK on Tuesday unveiled a lawsuit filed against Moderna in Delaware federal court, alleging that its patented inventions provide the “foundation” for Moderna’s mRNA vaccine portfolio. GSK said it’s looking to recover “a reasonable royalty” for Moderna’s tens of...
Gene Therapy Automatically Converts Omega-6 to Omega-3 Fatty Acids in the Body
Shriners Children's Develops New Technology to Prevent Childhood Obesity ST. LOUIS, Oct. 16, 2024 /PRNewswire/ -- According to the Centers for Disease Control, nearly 20% of children and teens are considered obese. Research shows it can have a dramatic impact on a...
Related Services