Ural E, Kesenci K, Fambri L, Migliaresi C, Piskin E
Department of Chemical Engineering, Hacettepe University, TUBITAK-Center of Excellence: POLBITEK, Beytepe, Ankara, Turkey.
Biomaterials. 2000 Nov;21(21):2147-54. doi: 10.1016/s0142-9612(00)00098-3.
In this study, elastomeric D,L-lactide and epsilon-caprolactone copolymers with two different molecular weights (Mn: 108.000 and 40.000) were synthesized by ring-opening polymerization of the respective dimers by using stannous octoate as the catalyst, as a potential bone-filling material. The final ratio of D,L-lactide to epsilon-caprolactone obtained by 1NMR was 60/40 (comparing to the initial ratio of 50/50). Both copolymers were amorphous having Tg at around -21 degrees C. Different amounts of hydroxyapatite (HA) powder were loaded within the copolymers. These composites were easily shaped by hand. Mechanical properties of the composites changed with the HA loading and the molecular weight of the copolymer. The percent elongation decreased, while both the Young's modulus and yield point (stress) increased with the HA content. The copolymers were degraded within the Ringer solutions in about 6 weeks. The molecular weight distribution became broader during degradation. Incorporation of HA reduced the degradation rate.
在本研究中,以辛酸亚锡为催化剂,通过相应二聚体的开环聚合反应,合成了两种不同分子量(Mn:108,000和40,000)的弹性体D,L-丙交酯和ε-己内酯共聚物,作为一种潜在的骨填充材料。通过1NMR得到的D,L-丙交酯与ε-己内酯的最终比例为60/40(初始比例为50/50)。两种共聚物均为无定形,玻璃化转变温度约为-21℃。在共聚物中加入了不同量的羟基磷灰石(HA)粉末。这些复合材料易于手工成型。复合材料的力学性能随HA负载量和共聚物分子量的变化而变化。随着HA含量的增加,伸长率百分比降低,而杨氏模量和屈服点(应力)均增加。共聚物在林格氏溶液中约6周内降解。降解过程中分子量分布变宽。HA的加入降低了降解速率。