Results for Lipids ( 1780 )
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YHS-12 is an ionizable lipid used to generate lipid nanoparticles to deliver RNA. LNPs optimized with the formula 15:10:25:2.5 (YHS-12/DOPE/cholesterol/DMG-PEG) delivered mRNA and siRNA together to Raw264.7-Luc cells. YHS-12 LNPs incorporating CRV peptide were able to target monocytes in situ to deliver MRSA-targeted chimeric antigen receptor (CAR) mRNA (SasA-CAR mRNA) and CASP11 siRNA. The engineered monocytes showed increased bactericidal activity in a MRSA-induced mouse model.
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Harashima group from Hokkaido University developed a hepatocyte-specific drug delivery system called multifunctional envelope-type nanodevice (MEND) which gives improved siRNA endosomal escape efficiency. The three generations of the pH-responsive ionizable lipid of the MEND system are YSK05 (2012 pKa 6.4) YSK13 (2016 pKa 6.45) and CL4H6 (2019 pKa 6.25). The ED50Â of Factor VII knockdown after the intravenous injection of YSK05 YSK13 and CL4H6 LNPs into mice were shown to be 60 ug/kg 15 ug/kg 2.5Â ug/kg respectively.
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ssPalmE-P4C2 is an ionizable lipid with a Vitamin E scaffold that is used to formulate lipid nanoparticles (LNPs) for delivering RNA into cells. The Vitamin E scaffold acts as an adjuvant to activate innate immune signaling. Vaccination with ssPalmE-P4C2 containing LNPs protected against lethal infection by Toxoplasma gondii in a mouse model.
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6 6’-trehalose dioleate is a glycolipid which can reduce toxicity when incorporated into lipid nanoparticles (LNPs). It can form hydrogen bonds with polar biomolecules allowing the formation of a stable LNP structure by partially replacing the ionizable lipid. It can facilitate the development of safe mRNA vaccines with improved clinical safety.
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Lipid M is an ionizable lipid used to form lipid nanoparticles for delivering RNA. LNPs formulated with Lipid M delivered luciferase mRNA in mice resulting in higher protein expression compared to the benchmark lipid DLin-MC3-DMA. Lipid M LNPs delivering IgG mRNA showed prolonged expression compared to MC3 in non-human primates after intramuscular injection.
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4-O10b1 is an ionizable lipid used to generate lipid nanoparticles (LNPs) for delivering RNA to cells. LNPs comprised of 4-O10b1 and conjugated with the macrophage antibody F4/80 were able to delivery siRNA targeting TAK1 to RAW264.7 cells resulting in suppressed activation of NF-kB. Intranasal administration reduced lung injury in an influenza mouse model.