Amsden Brian G, Misra Gauri, Gu Frank, Younes Husam M
Department of Chemical Engineering, Queens University, Kingston, Ontario, Canada, K7L 3N6.
Biomacromolecules. 2004 Nov-Dec;5(6):2479-86. doi: 10.1021/bm049578h.
The synthesis and characterization of a photocurable biodegradable elastomer as a potential biomaterial for the delivery of thermosensitive drugs are described. The elastomer was prepared from UV initiated cross-linking of an acrylated star-poly(epsilon-caprolactone-co-D,L-lactide) prepolymer. The influence of the molecular weight of the acrylated prepolymer on the final elastomer mechanical and thermal properties was determined. The glass-transition temperature of the elastomers was independent of the prepolymer molecular weight and was from -6 to -8 degrees C. The Young's modulus and stress at break of the elastomers was proportional to the inverse of the prepolymer molecular weight, while the strain at break increased in a linear fashion with the prepolymer molecular weight. Over a degradation period of 12 weeks in phosphate buffered saline, the elastomers exhibited little mass loss, appreciable mechanical strength loss, and little dimensional or strain at break change.
本文描述了一种可光固化的可生物降解弹性体的合成与表征,该弹性体作为一种潜在的生物材料用于热敏药物的递送。该弹性体由丙烯酸化星形聚(ε-己内酯-co-D,L-丙交酯)预聚物通过紫外线引发交联制备而成。测定了丙烯酸化预聚物的分子量对最终弹性体力学和热性能的影响。弹性体的玻璃化转变温度与预聚物分子量无关,为-6至-8摄氏度。弹性体的杨氏模量和断裂应力与预聚物分子量的倒数成正比,而断裂应变随预聚物分子量呈线性增加。在磷酸盐缓冲盐水中12周的降解期内,弹性体质量损失很小,机械强度有明显损失,断裂时尺寸或应变变化很小。