Table 1.
Conventional preparation methods of liposomes and their characteristics.
| Methods | Advantages | Disadvantages | References |
|---|---|---|---|
| Thin-film hydration method | Simple and maneuverable, this method of production allows for quick and easy production |
|
[26,35] |
| Reverse evaporation | Because liposomes contain more aqueous phase, they are ideal for encapsulating proteins or large molecules like DNA, RNA, and other drugs. |
|
[27,36] |
| Double emulsion method | Multicapsule structures with a non-concentric structure are better suited to encapsulating water-soluble drugs to increase their encapsulation rate, and they have slow release characteristics. | The particle size of non-concentric multivesicular liposomes is larger than that of other types and their stability is lower than that of other liposome types. | [28] |
| Freeze drying method | Long-term storage is possible with the preparation as it is very stable. | Higher production costs due to long freeze-drying processes. | [30,37,38] |
| Ethanol injection method | Some unstable drugs can be loaded with this process because it is simple, fast, and reduces the exposure of lipid and encapsulants. |
|
[31,39] |
| Active loading methods | In situations where pH and ionic strength are strongly influencing the oil-water partition coefficient, this methods is ideal. | Liposomes can only contain weakly basic or weakly acidic drugs, and drugs must not have an electrical charge in order to be loaded into them. | [33,40] |