“…Besides the positive charge, the presence of a lipophilic tail, as well as the hydrophobic amino acids in the polymyxin peptide structure, allows the use of both amphiphilic and hydrophobic low-molecular compounds and polymers for drug delivery. Therefore, the delivery systems considered for polymyxins include anionic liposomes [ 22 , 23 , 24 , 25 ], lipid NPs [ 26 , 27 ], and different polymer systems [ 28 , 29 , 30 ]. The polymers include hydrophobic poly(butyl cyanoacrylate)-based NPs [ 29 ], poly( l -lactide)/halloysite nanotube nanofiber mats for wound treatment [ 30 ], and hybrid systems based on alginate-cross-linked polymyxin B loaded into lipid NPs [ 28 ].…”