Table 2.
Polymers used in biodegradable microspheres | polymers | FDA approved for eye use | advantages | disadvantages |
---|---|---|---|---|
Natural biodegradable polymers | Gelatin | Yes | Easily derived, biocompatible, less immunogenic, low cost | Strength depends on source and processing conditions, challenging to safely crosslink |
Alginic acid | Yes | gel forming ability | Poor mechanical strength | |
chitosan | No | mucosal adhesion, in-situ gelation, transfection, and permeation-enhancing capabilities | Insoluble in neutral or alkaline, solutions, strong electrostatic behavior | |
Pectin | No | gel-forming properties, mucosal adhesion | Lack of clinical data | |
Synthetic biodegradable polymers | PLA | Yes | Synthesized from natural sources, easily processed, slow degradation rate | Acidic degradation by products |
PLGA | Yes | water soluble, tunable degradation rate | Acidic degradation by products | |
PEG | Yes | water soluble, biocompatible | Fast degradation compared to other synthetic polymers | |
PCL | No | easily modified, inexpensive | Poor mechanical properties | |
PEA | No | Enhanced biocompatibility and excellent mechanical properties | Lack of clinical data | |
PCADK | No | excellent biocompatibility and biodegradability properties | Degrades slowly in vivo |
Abbreviations:PLA, polylactic-lactic acid; PLGA, polylactic-glycolic acid; PEG, poly (ethylene glycol); PCL, poly (ε-caprolactone); PEA, polyester amide; PCADK, poly (cyclohexane-1,4-diyl acetone dimethylene ketal).