Table 1.
Method | Advantages | Disadvantages | Liposomes Diameter | Reference |
---|---|---|---|---|
Electroformation | Simple and rapid | Large size polydisperisity, inapplicable to ionic solutions, low encapsulation efficiency | 5–150 μm | [24,25] |
Hydration | Electric fields are unnecessary | Large size polydisperisity, products are multilamellar; sensitive to phospholipid type and physical conditions, low encapsulation efficiency |
1–10 μm | [24] |
Extrusion | Reduced size polydispersity | Relatively complex in operation | 130–370 nm | [28] |
Microfluidic jetting | Products are unilamellar and of controlled size, encapsulation efficiencies are high | Specialized equipment needed, sensitivity to operational parameters and types of materials used | Above 100 μm | [29] |
Microfluidic hydrodynamic-focusing | Products are monodisperse, the size and lamellarity of liposomes are easily controlled, high-throughput production | Low liposome concentration in the end-product | 50–300 nm | [30] |
Droplet emulsion templates | Polymerosomes can be generated, the size and structure of products can be controlled, high encapsulation efficiencies | Solvent may reside between monolayers | 20–200 μm | [31] |