Lu Jianxi, Blary Marie-Claude, Vavasseur Sébastien, Descamps Michel, Anselme Karine, Hardouin Pierre
Laboratoire de Recherche sur les Biomatériaux et les Biotechnologies (LR2B), Université du Littoral Côte d'Opale, 52 Rue Du Docteur Calot, 62608 Berck sur Mer Cedex, France.
J Mater Sci Mater Med. 2004 Apr;15(4):361-5. doi: 10.1023/b:jmsm.0000021102.68509.65.
We performed experimental studies to confirm the hypothesis that cellular damages occurring around implanted biphasic bioceramics could be related to a micro-particles release because of an insufficient sintering. First, an in vitro cytotoxicity study was performed on four biphasic ceramic (BCP) samples. Without treatment of the extraction medium, a cytotoxicity was observed, although after centrifugation this cytotoxicity disappeared in all samples. Second, micro-particles of hydroxyapatite (HA), beta-tricalcium phosphate (beta-TCP) and 40% beta-TCP/60%HA mixture were used for a cell inhibition study. A decrease of cell viability was observed with the increase in particles concentration. At 10000 particles per cell, the viability and proliferation were completely inhibited. Third, HA, beta-TCP and BCP ceramic granules were implanted in rabbit femoral cavities for 12 weeks. No degradation of HA granules was observed. The degradation was higher for beta-TCP (40%) than for BCP (5%). On the other hand, new bone formation was significantly higher for beta-TCP (21%) and HA (18%) than for BCP (12%). More micro-particles were formed around BCP granules than around beta-TCP, and phagocytised by macrophages. The release of ceramic micro-particles could be related to the sintering process. BCP ceramic have to be sintered at only 1160 degrees C. Consequently, HA micro-particles of BCP ceramic are incompletely sintered and easily released after immersion or implantation. The microparticles could be at the origin of local inflammation and cell damage and could perhaps modify osteogenesis. Attention must be paid to this problem especially with BCP ceramics because of the sintering difficulties of this bioceramic.
我们进行了实验研究,以证实以下假设:植入的双相生物陶瓷周围发生的细胞损伤可能与烧结不足导致的微粒释放有关。首先,对四个双相陶瓷(BCP)样品进行了体外细胞毒性研究。在未处理提取介质的情况下,观察到了细胞毒性,不过在离心后,所有样品中的这种细胞毒性均消失。其次,使用羟基磷灰石(HA)、β-磷酸三钙(β-TCP)和40%β-TCP/60%HA混合物的微粒进行细胞抑制研究。随着颗粒浓度的增加,观察到细胞活力下降。在每细胞10000个颗粒时,活力和增殖完全受到抑制。第三,将HA、β-TCP和BCP陶瓷颗粒植入兔股骨腔12周。未观察到HA颗粒的降解。β-TCP(40%)的降解高于BCP(5%)。另一方面,β-TCP(21%)和HA(18%)的新骨形成明显高于BCP(12%)。BCP颗粒周围形成的微粒比β-TCP周围更多,并被巨噬细胞吞噬。陶瓷微粒的释放可能与烧结过程有关。BCP陶瓷仅需在1160摄氏度下烧结。因此,BCP陶瓷的HA微粒烧结不完全,在浸泡或植入后容易释放。这些微粒可能是局部炎症和细胞损伤的根源,并且可能会改变骨生成。由于这种生物陶瓷烧结困难,对于BCP陶瓷尤其要注意这个问题。