Plasticizing effect of water on poly(lactide-co-glycolide)

The purpose of this research was to evaluate the effect and nature of hydration on the glass transition temperature ( T g) of poly( d, l-lactide-co-glycolide) and investigate the physical state of water within the polymer during hygrothermal aging. The polymer was incubated in water at 23, 30, 37 an...

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Veröffentlicht in:Journal of controlled release 2005-11, Vol.108 (1), p.1-9
Hauptverfasser: Blasi, Paolo, D'Souza, Susan S., Selmin, Francesca, DeLuca, Patrick P.
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Sprache:eng
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Zusammenfassung:The purpose of this research was to evaluate the effect and nature of hydration on the glass transition temperature ( T g) of poly( d, l-lactide-co-glycolide) and investigate the physical state of water within the polymer during hygrothermal aging. The polymer was incubated in water at 23, 30, 37 and 55 °C, while the vapor sorption studies were carried out at 37 °C using saturated salt solutions. The water content and the thermal behavior of PLGA-water system were assessed by Karl Fischer titration and modulated differential scanning calorimetry, respectively, the hygrothermal aging was monitored by gel permeation chromatography. Water depressed reversibly the T g by about 15 °C regardless of the incubation conditions. The T g then remained constant at ∼30 °C for five days, except when degradation occurred. A broad ice melting peak was detected around 0 °C. In the sorption studies, a linear correlation ( r 2 0.9837) between the T g and the moisture content was observed in the range of 0.3–2.6% w/w, but there was no discernible endothermic event associated with the melting of ice. Data were found to fit reasonably well to the Gordon–Taylor/Kelley–Bueche equation. There were no differences between bulk and vapor water aging. It is proposed that the water responsible for plasticizing the polymer was non-freezable (bound) water and the small fraction of such water which was absorbed at high relative humidity caused polymer degradation in the same manner as bulk water.
ISSN:0168-3659
1873-4995
DOI:10.1016/j.jconrel.2005.07.009