Aydin H M, Salimi K, Rzayev Z M O, Pişkin E
Institute of Science, Bioengineering Division, Hacettepe University, Beytepe, 06800, Ankara, Turkey.
Biomater Sci. 2013 May 2;1(5):503-509. doi: 10.1039/c3bm00157a. Epub 2013 Feb 25.
Poly(glycerol-sebacate) (PGS) was introduced a decade ago as a potential material for soft tissue repair. All of the proposed copolymerization reactions in the literature include a two-stage (prepolymerization and curing) synthesis where the reaction times can take as long as several days. This study, on the other hand, proposes a new route that eliminates these disadvantages and enables a rapid synthesis of PGS elastomers via microwave-assisted prepolymerization in minutes instead of days. No purge gas, catalyst or vacuum is needed in the first prepolymerization step. The curing stage was carried out at 150 °C for 4, 8, 16, and 24 hours. The glass transition temperature (T) and melting temperatures for the glycerol and sebacic acid fragments (T and T ) of these PGS elastomers were found as -35.61 °C, -15.82 °C, and 61.70 °C, respectively. The Young's modulus and tensile strength values were found as 0.50 ± 0.02 MPa and 0.27 ± 0.06 MPa, respectively.
聚(甘油-癸二酸酯)(PGS)在十年前作为一种潜在的软组织修复材料被引入。文献中所有提出的共聚反应都包括两阶段(预聚合和固化)合成,其中反应时间可能长达数天。另一方面,本研究提出了一种新方法,该方法消除了这些缺点,并能够通过微波辅助预聚合在几分钟而非几天内快速合成PGS弹性体。在第一个预聚合步骤中不需要吹扫气体、催化剂或真空。固化阶段在150°C下进行4、8、16和24小时。这些PGS弹性体的甘油和癸二酸片段的玻璃化转变温度(T)和熔点(T 和 T )分别为-35.61°C、-15.82°C和61.70°C。杨氏模量和拉伸强度值分别为0.50±0.02MPa和0.27±0.06MPa。