The invention belongs to the technical field of pharmaceutical preparations and
nanomedicine, and relates to a bionic nano-
drug for preventing and treating
aortic dissection, in particular to a mononuclear / macrophage membrane bionic modified multidrug co-loaded anti-inflammatory
liposome and a preparation method thereof. The
liposome is composed of cationic
phospholipid and neutral
phospholipid, co-loading of multiple anti-inflammatory drugs can be achieved in the
liposome, anti-
inflammatory cell-penetrating
peptide is covalently modified on the surface of the liposome, and then mononuclear / macrophage
membrane protein is used for bionic modification. According to the bionic anti-inflammatory liposome, multiple receptors and adhesion molecular ligands mediated and chemotactic on the surface of a mononuclear / macrophage membrane are utilized to realize a natural targeting effect on an inflammatory site, and non-specific clearance of a reticuloendothelial
system (RES) to the liposome is reduced by virtue of modification of leukocyte self-recognition molecules. The bionic anti-inflammatory lipidosome can effectively cross a vascular endothelial barrier, gather and release anti-inflammatory drugs at the early
lesion part of the
aortic dissection in a targeted manner, play a synergistic anti-inflammatory role, inhibit
inflammation-related cells from
chemotaxis and infiltration into the
lesion part, and further prevent and treat the occurrence and development of the
aortic dissection.