Journal
BIOMATERIALS
Volume 26, Issue 14, Pages 2137-2145Publisher
ELSEVIER SCI LTD
DOI: 10.1016/j.biomaterials.2004.06.033
Keywords
controlled drug release; degradation; hydrolysis; poly(lactic acid); poly(glycolic acid)
Funding
- NIAID NIH HHS [R24-AI47739-02] Funding Source: Medline
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The component materials of controlled-release drug delivery systems are often selected based on their degradation rates. The release time of a drug from a system will strongly depend on the degradation rates of the component polymers. We have observed that some poly(lactic-co-glycolic acid) polymers (PLGA) exhibit degradation rates that depend on the size of the polymer object and the temperature of the surrounding environment. In vitro degradation studies of four different PLGA polymers showed that 150 mum thick membranes degraded more rapidly than 50 pm thick membranes, as characterized by gel permeation chromatography and mass loss measurements. Faster degradation was observed at 37degreesC than 25degreesC, and when the saline media was not refreshed. A biodegradable polymeric microreservoir device that we have developed relies on the degradation of polymeric membrane, to deliver pulses of molecules from reservoirs on the device. Earlier molecular release was seen from devices having thicker PLGA membranes. Comparison of an in vitro release study from these devices with the degradation study suggests that reservoir membranes rupture and drug release occurs when a membrane threshold molecular weight of 5000-15000 is reached. (C) 2004 Elsevier Ltd. All rights reserved.
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