Habraken W J E M, Wolke J G C, Mikos A G, Jansen J A
Department of Periodontology and Biomaterials, College of Dental Science, Radboud University Nijmegen Medical Centre, P.O. Box 9101, 6500 HB Nijmegen, The Netherlands.
J Biomater Sci Polym Ed. 2006;17(9):1057-74. doi: 10.1163/156856206778366004.
Calcium phosphate (CaP) cements show an excellent biocompatibility and often have a high mechanical strength, but in general degrade relatively slow. To increase degradation rates, macropores can be introduced into the cement, e.g., by the inclusion of biodegradable microspheres into the cement. The aim of this research is to develop an injectable PLGA microsphere/CaP cement with sufficient setting/cohesive properties and good mechanical and physical properties. PLGA microspheres were prepared using a water-in-oil-in-water double-emulsion technique. The CaP-cement used was Calcibon, a commercially available hydroxyapatite-based cement. 10:90 and 20:80 dry wt% PLGA microsphere/CaP cylindrical scaffolds were prepared as well as microporous cement (reference material). Injectability, setting time, cohesive properties and porosity were determined. Also, a 12-week degradation study in PBS (37 degree C) was performed. Results showed that injectability decreased with an increase in PLGA microsphere content. Initial and final setting time of the PLGA/CaP samples was higher than the microporous sample. Porosity of the different formulations was 40.8% (microporous), 60.2% (10:90) and 69.3% (20:80). The degradation study showed distinct mass loss and a pH decrease of the surrounding medium starting from week 6 with the 10:90 and 20:80 formulations, indicating PLGA erosion. Compression strength of the PLGA microsphere/CaP samples decreased siginificantly in time, the microporous sample remained constant. After 12 weeks both PLGA/CaP samples showed a structure of spherical micropores and had a compressive strength of 12.2 MPa (10:90) and 4.3 MPa (20:80). Signs of cement degradation were also found with the 20:80 formulation. In conclusion, all physical parameters were well within workable ranges with both 10:90 and 20:80 PLGA microsphere/CaP cements. After 12 weeks the PLGA was totally degraded and a highly porous, but strong scaffold remained.
磷酸钙(CaP)骨水泥具有优异的生物相容性,通常还具有较高的机械强度,但总体降解相对缓慢。为了提高降解速率,可以在骨水泥中引入大孔,例如通过在骨水泥中加入可生物降解的微球。本研究的目的是开发一种具有足够凝固/粘结性能以及良好机械和物理性能的可注射PLGA微球/CaP骨水泥。采用水包油包水双重乳液技术制备PLGA微球。所用的CaP骨水泥是Calcibon,一种市售的羟基磷灰石基骨水泥。制备了10:90和20:80干重百分比的PLGA微球/CaP圆柱形支架以及微孔骨水泥(参考材料)。测定了可注射性、凝固时间、粘结性能和孔隙率。此外,还在PBS(37℃)中进行了为期12周的降解研究。结果表明,随着PLGA微球含量的增加,可注射性降低。PLGA/CaP样品的初始和最终凝固时间高于微孔样品。不同配方的孔隙率分别为40.8%(微孔)、60.2%(10:90)和69.3%(20:80)。降解研究表明,从第6周开始,10:90和20:80配方的样品出现明显的质量损失以及周围介质pH值下降,表明PLGA发生了侵蚀。PLGA微球/CaP样品的抗压强度随时间显著降低,微孔样品保持不变。12周后,两种PLGA/CaP样品均呈现球形微孔结构,抗压强度分别为12.2MPa(10:90)和4.3MPa(20:80)。在20:80配方中也发现了骨水泥降解的迹象。总之,10:90和20:80的PLGA微球/CaP骨水泥的所有物理参数均在可行范围内。12周后,PLGA完全降解,留下了一个高度多孔但坚固的支架。