“…A qualified vehicle for siRNA delivery should significantly enhance its biostability, facilitate the endocytosis, and enrich the siRNA in the target location. To date, numerous vehicles have been developed for siRNA delivery, including lipid/polymer nanoparticles, , amphiphilic dendrimers, DNA carriers, , peptide/protein assemblies, â graphene oxide, mesoporous silica, , gold nanoparticles/nanorods, ,, black phosphorus, etc. However, limitations, including cytotoxicity, serious non-specific absorption, and poor colloidal stability in bio-medium, still accompany these delivery methods.…”