Liposomes are promising delivery vehicles and offer the added drawcard of being able to be made functional to target tissues such as cardiac muscle and cancerous cells. Current methods to manufacture liposomes need to be improved and supercritical fluid (SCF) technologies may offer a solution. Herein, the dispersibility of six different phospholipids (PLs): determined using supercritical carbon dioxide (scCO 2), and 1,2-distearoyl-sn-glycero-3phosphocholine (DSPC) showed highest post-processing dispersibility, while 1,2-dioleoyl-snglycero-3-phosphocholine (DOPC), 1,2-dioleoyl-sn-glycero-3-phosphoethanolamine, (DOPE) and 1,2-dioleoyl-3-trimethylammonium-propane (DOTAP) showed no dispersibility at all in scCO 2 at the assessed experimental conditions. The zetasizer results showed that the SCF conditions at 37 °C, 250 bar and 200 RPM for 60 min provided nanoparticles with narrowest polydispersity index (PDI) and spherical shaped as shown by cryo-transmission electron microscopy (Cryo-TEM) supported these results. The mean diameter of liposomes using the SCF method for DSPC-PEGylated and DOPC-PEGylated liposomes was 98.3±3.3 nm and 124.5±4.1 nm, while using thin film method it was 153.6 ± 4.5 nm and 131.3±3.4 nm, respectively. The stability of liposomes stored at different temperatures (25 °C, 4 °C and-20 °C) using SCF technology was better over a period of 3 months. The current study would provide green alternative method, less laborious, save time and energy.