Table 6.
Method | Main Characteristic | Resulted Porosity | Cell Viability |
Ref. |
---|---|---|---|---|
Freeze casting | Ceramic slurries are used in this method; then, water is evaporated. It produces pores due to formation of ice crystals. | <85% | <90% | [237] |
Freeze-drying | It is an easy procedure that can be applied with natural materials such as collagen and fibers. The porosity can be improved by freezing temperature alterations and changing of the concentration of materials. |
30%–80% | <90% | [238] |
Solvent casting and Particle leaching | It uses casting molds to produce 3D scaffolds by polymer solution. Then, it requires leaching by using organic solvents to simplify the addition of drugs or growth factors to scaffolds. |
50%–90% | 75%–88% | [239] |
Gas foaming | Using high-pressure carbon dioxide for expanding the polymer matrix without applying high temperature or toxic solvents. Changing pressure can also create scaled porous scaffolds. | <90% | N/A | [240] |
Phase separation | Changing temperature for polymer and solvent separation results in a solid polymer due to phase separation. Finally, a desirable, homogenous, and interconnected porous scaffold is produced depending on cooling rates. |
60%–98% | <98% | [241] |
Electrospinning | Nanoscale or microscale fibers are produced by tuning process parameters and chemicals in this method. | 80%–95% | <80% | [242,243] |
Sol–gel | Colloidal metal oxides are applied traditionally to create tunable porous scaffolds in the sol–gel method with desirable chemistry. Double phasic chitosan scaffolds with a conjunction peptide have demonstrated the capability to recruit stem cells for cartilage repair. |
N/A | N/A | [244] |
Additive manufacturing | Extrusion methods in biomedical applications are often polymer-based and provide benefits in cost, size, and flexibility against old manufacturing methods. Both polymers and metals can be used in solid free-form sintering, while laser melting is limited to metals. |
80%–90% | 60%–95% | [245] |