Table 1.
Advantages | Disadvantages | |
---|---|---|
Electrospinning | • Easy to setup | • Poor cell infiltration into the core of the scaffolds |
• Cost effective | • 2-Dimensional pore or microstructure arrangement |
|
• High level of versatility allows control over fiber diameter, microstructure and arrangement |
• Toxic solvents often used | |
• Vast materials selection | ||
Self Assembly | • Easy incorporation of cells during fiber formation |
• Complex procedure |
• 3-Dimensional pore arrangement | • Lack of control of fiber orientation and arrangement |
|
• Injectable for in vivo assembly | • Limited fiber diameter ~2–30 nm and length ~10 µm |
|
Phase Separation | • 3-Dimensional pore arrangement | • Complex procedures |
• Lack of control of fiber arrangement | ||
Bacterial Cellulose | • Low cost | • Limited material selection |
• High yield | • Lack of versatility for functionalization |
|
Templating | • Vast materials selection | • Sacrificial materials |
• Control over fiber diameter and length |
• Limitation on fiber dimensions and arrangement |
|
Drawing | • Vast materials selection | • Low productivity (One single fiber at a time) |
• Simple procedure | • Difficult to form fibers with consistent diameter | |
Extraction | • Natural materials | • Limited material selection |
• Limited control of fiber diameter and length (a few microns) |
||
Vapor-Phase Polymerization | • Polymer synthesized directly into nanofibers |
• Limited control of fiber diameter and length (hundreds of microns) |
• Limited material selection | ||
• Complicated procedures | ||
Kinetically controlled solution synthesis | • Polymers synthesized directly into nanofibers |
• Limited control of fiber diameter and length (60 µm) |
• Limited material selection | ||
• Complicated procedures | ||
Chemical Polymerization of Aniline | • Polymers synthesized directly into nanofibers |
• Limited control of fiber diameter and length |
• Limited material selection | ||
• Complicated procedures |