Modulating the drug release from polyester matrices independently from the material properties would be beneficial to those designing biodegradable medical implants, such as drug delivery devices, stents and screws. We propose that modulated drug release can be obtained via an additive-free mechanism in polyesters by simply controlling polymer erosion through acidic terminal functional groups. The formulations can be tuned to produce large ranges in drug release with relatively small changes in terminal acidic functional groups. For example, poly(lactic-co-glycolic acid) (PLGA) 53/47 thin films could be tuned to have 10–90% drug release at 20 days, depending on the concentration of acidic terminal groups.
- Terry W J Steele
- Charlotte L Huang
- Subbu S Venkatraman
