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Preparation method | Advantages | Disadvantages |
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Conventional methods | | |
High homogenization | Large-scale production, high encapsulation efficiency | Deactivation of core material in nanocarrier |
Solvent injection (ethanol or ether) | Ability to control vesicle size | Dilution of nanocarrier, heterogeneous population, use of high temperature |
Reverse phase evaporation | High encapsulation efficiency, economic | Organic solvent traces, not suitable for fragile molecules or food ingredients |
Solvent-emulsification | High encapsulation efficiency | Multivesicular, unstable |
Postformation processing | Reduced processing time, high encapsulation efficiency | Low lamellarity and heterogeneity |
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Emerging methods | | |
Microfluidic channel method | Synthesis of monodisperse nanocarrier, high encapsulation efficiency | Fabrication could be complex and needs optimization |
Supercritical fluid method | Control over particle formation, easily translated to large-scale production, environment-friendly | Elevated pressure and temperatures |
Self-assembly method | Handy and controllable method for changing the shape of nanocarriers | Poorly understood experimental conditions |
Spray drying | Environment-friendly process, high encapsulation efficiencies | Expense and time-required |
Freeze drying of monophase solutions | Monodisperse nanocarrier that can be stored for a long time in a sealed container | Time-required |
Membrane contactor method | Nanocarriers have homogeneous and small size, high encapsulation efficiency, simplicity for scale-up | Hydrophilic drug encapsulation needs optimization |
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