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.