Table 1.
Fabrication Methods | Materials | Advantages/Disadvantages | Size Range |
---|---|---|---|
Emulsification and solvent evaporation | PLGA [10], Chitosan [11], Gelatin [12], PCL/HA [13], Collagen [14], Collagen/chitosan [15] | Simple to operate Limited control over microsphere sizes |
A few hundred nanometers to several millimeters |
Spray drying | PLA [16], Chitosan [17], Alginate/HA [18] | Simple to operate Convenient to encapsulate bioactive molecules in microspheres Uncontrollable particle size and morphology |
A few micrometers to several hundred micrometers |
Phase separation | PLGA [19], Poly(l-glutamic acid)/chitosan [20], Chitosan [21] | Porous microspheres Effective for only a few polymers |
A few micrometers to several millimeters |
Microfluidics | PLGA [22], Bacterial cellulose [23], PCL [24] | Well controlled microsphere sizes Convenient drug loading Low productivity Time consuming |
A few micrometers to several millimeters |
Electrospray | PLGA [25], PLA [26], PCL/gelatin [27], | Simple to operate Uncontrollable particle size and morphology |
A few micrometers to several hundred micrometers |