Table 1.
Methods | Advantages | Disadvantages | |
---|---|---|---|
High energy methods | High pressure homogenization (hot homogenization and cold homogenization) | Widely used method for the preparation of SLNs and NLCs Hot method is used to heat stable materials whereas cold method is used for thermo-labile drugs |
Polydisperse distributions and unproven scalability |
Microwave-assisted | This method is not frequently used | – | |
Ultrasonication | Reduced shear stress and less time consuming | Contamination of metals may occur | |
Supercritical fluid technique | No solvent is used as CO2 acts as a solvent Particles are obtained as dry powder |
Very expensive method | |
Low energy methods | Microemulsion-based technique | No sophisticated machines are required for the preparation of microemulsion Less energy is required |
Highly diluted dispersions of particles are obtained |
Double emulsion | Production of SLN-containing peptides and hydrophilic active ingredients | Particle growth will occur on storage | |
Membrane contactor technique | Applicable for large-scale production | – | |
Phase Inversion technique | Suitable for thermo-labile drugs | Tedious process | |
Organic solvent-based methods | Solvent emulsification-diffusion technique | Most used method for the preparation of the NLCs | Solvent may interact with the drug molecule |
Solvent emulsification-evaporation technique | Most used method for the preparation of SLNs | Solvent may interact with the drug molecule | |
Solvent injection technique | Easy handling and fast production process | Solvent may interact with the drug molecule |