890907 | cKK-E12
3,6-bis(4-(bis(2-hydroxydodecyl)amino)butyl)piperazine-2,5-dione
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cKK-E12
3,6-bis(4-(bis(2-hydroxydodecyl)amino)butyl)piperazine-2,5-dione
cKK-E12 is considered a multi-tail ionizable lipidoid and was originally developed to improve the efficacy and safety of siRNA delivery systems. In the original study, cKK-E12 lipid nanoparticle formulations consisting of 50 mol% cKK-E12, 10 mol% cholesterol, 38.5 mol% DSPC, and 1.5 mol% DMG-PEG2000 showed silencing of hepatocytes and high selectivity toward liver parenchymal cells in mice and non-human primates.1
Although cKK-E12 was originally developed for delivery of siRNA, it has proven to also be useful for the delivery of mRNA. Below is a sample of recent research studies conducted using cKK-E12 to deliver mRNA:
- cKK-E12 mRNA-LNPs were used to engineer dendritic cells ex-vivo for cancer therapies.2
- mRNA-LNP formulations containing cKK-E12 exhibited efficient T cell expansion and cytokine production ex vivo.3
References:
1. Y. Dong, K.T. Love, J.R. Dorkin, S. Sirirungruang, Y. Zhang, D. Chen, R.L. Bogorad, H. Yin, Y. Chen, A.J. Vegas, C.A. Alabi, G. Sahay, K.T. Olejnik, W. Wang, A. Schroeder, A.K.R. Lytton-Jean, D.J. Siegwart, A. Akinc, C. Barnes, S.A. Barros, M. Carioto, K. Fitzgerald, J. Hettinger, V. Kumar, T.I. Novobrantseva, J. Qin, W. Querbes, V. Koteliansky, R. Langer, & D.G. Anderson, Lipopeptide nanoparticles for potent and selective siRNA delivery in rodents and nonhuman primates, Proc. Natl. Acad. Sci. U.S.A. 111 (11) 3955-3960, https://doi.org/10.1073/pnas.1... (2014).
2. R. Das, X. Ge, F. Fei, S. Parvanian, R. Weissleder, C. S. Garris, Lipid Nanoparticle-mRNA Engineered Dendritic Cell Based Adoptive Cell Therapy Enhances Cancer Immune Response. Small Methods 2025, 9, 2400633. https://doi.org/10.1002/smtd.202400633
3. Biomater. Sci., 2023,11, 964-974 https://doi.org/10.1039/D2BM01581A
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