TABLE 2.
Advantages and limitations of synthetic biomaterials for skeletal muscle regeneration.
| Synthetic polymers | Advantages | Disadvantages | Citations |
|---|---|---|---|
| PCL | High Young’s modulus, stiffness | Does not support cell proliferation or differentiation alone | Sundelacruz and Kaplan (2009), Kim et al. (2010), Sánchez-Cid et al. (2021) |
| New muscle growth when coated with natural biomaterials | Long degradation times | ||
| PLGA | Mild support of differentiation | Lower elastic modulus when combined with natural biomaterials | Boateng et al. (2005), Aviss et al. (2010), Shin et al. (2015), Wang et al. (2021) |
| Good differentiation when coated with natural materials | Acidic degradation products | ||
| PEG | Hydrophilic | Does not support proliferation or differentiation alone | Fuoco et al. (2015), Kutikov and Song (2015), Wang et al. (2019) |
| New muscle growth when coated with biomaterials | Requires functionalization to degrade | ||
| Addition of PEG has plasticizing effect on hard polymers | |||
| PLLA | Grows functional muscle in combination with other biomaterials | More successful with protein coating | Scime et al. (2009), Lee et al. (2012), Wolf et al. (2015), Fitzgerald et al. (2018) |
| Recruits native SCs | Acidic degradation products | ||
| Supports vascularization | Long degradation times | ||
| PGA | Hydrophilic | Does not induce vascularization | Saxena et al. (2001), Fuchs et al. (2003), Kamelger et al. (2004), Miranda et al. (2021) |
| Rapid degradation | |||
| Acidic degradation products | |||
| PDMS | Grows 2D skeletal muscle films | Ineffective without combining with other natural materials | Fujita et al. (2009), Shen et al. (2013), Mueller et al. (2021) |
| Useful as a mold or patterned surface | Little in vivo research | ||
| Does not degrade in vivo |