Department of Bioengineering, Hanyang University, 17 Haengdang-dong, Seongdong-gu, Seoul 133-791, South Korea.
J Biomater Sci Polym Ed. 2010;21(5):635-45. doi: 10.1163/156856209X434656.
Previously, we developed an apatite-coated non-porous poly(lactic-co-glycolic acid) (PLGA) microsphere (ANPM) as an injectable bone substitute. We hypothesized that an apatite-coated porous PLGA microsphere (APPM) would have enhanced osteogenic potential compared to that of an ANPM. To test the hypothesis, critical-sized bone defects were made in mouse calvaria, and APPMs and ANPMs were implanted in the defects for 8 weeks. New bone formed around both types of bone substitutes implanted in mouse calvarial defects. Importantly, the portion of bone-like tissue area in the implant cross-sectional area was significantly higher in the APPM group than in the ANPM group (36.9% versus 14.6%, P < 0.001). Fluorochrome-labeling analysis showed that bone regeneration occurred in the pores of implanted APPMs. The results show that APPM may be useful as a bone substitute in orthopedic applications.
先前,我们开发了一种涂有磷灰石的非多孔聚(乳酸-共-乙醇酸)(PLGA)微球(ANPM)作为可注射性骨替代物。我们假设涂有磷灰石的多孔 PLGA 微球(APPM)与 ANPM 相比具有增强的成骨潜力。为了验证这一假设,在小鼠颅骨中制造了临界大小的骨缺损,并将 APPM 和 ANPM 植入缺损部位 8 周。在植入小鼠颅骨缺损的两种骨替代物周围都形成了新骨。重要的是,在 APPM 组中,植入物横截面积的类骨组织区域的比例明显高于 ANPM 组(36.9%比 14.6%,P <0.001)。荧光标记分析表明,骨再生发生在植入的 APPM 的孔中。结果表明,APPM 可用作骨科应用中的骨替代物。