Ohno Motofumi, Kimoto Kazunari, Toyoda Toshihisa, Kawata Kazushige, Arakawa Hirohisa
Department of Health Science, Kanagawa Dental College, Yokosuka, Japan.
J Oral Implantol. 2013 Apr;39(2):154-60. doi: 10.1563/AAID-JOI-D-10-00175. Epub 2011 Nov 22.
When resorbable hydroxyapatite (HA) granules, which are used as a bone supplement material, were treated in neutral 4% sodium fluoride (NaF) solution, formation of a reactant resembling calcium fluoride was observed on the surface of the granules. Immediate and slow release of fluoride from fluoridated HA (HA+F) granules was observed after immersion in culture fluid, and the concentration increased over time to 1.25 ± 0.05 ppm F at 0.5 hours, 1.57 ± 0.12 ppm F at 24 hours, and 1.73 ± 0.15 ppm F at 48 hours. On invasion assay, migration of human osteoblast-like MG-63 cells exposed to the released fluoride was confirmed in comparison to the cells incubated with a nonfluoridated control sample (P < .01). In addition, fluoride added to the medium increased MG-63 cell proliferation in a manner dependent on fluoride concentrations up to 2.0 ppm (P < .05). At 5.0 ppm, however, fluoride significantly inhibited cell proliferation (P < .005). Activity of the osteogenic differentiation marker, alkaline phosphatase (ALP), also increased with fluoride after exposure for 1 week, increasing significantly at 1.0 ppm (P < .05). The promotion of MG-63 cell migration and proliferation, as well as increased ALP activity, suggested that fluoride released from the surface of resorbable HA granules, which were fluoridated by prior treatment with neutral 4% NaF solution, can provide a superb method to supply fluoride and promote osteogenic cell differentiation.
当用作骨补充材料的可吸收羟基磷灰石(HA)颗粒在中性4%氟化钠(NaF)溶液中处理时,在颗粒表面观察到类似氟化钙的反应物形成。将氟化HA(HA + F)颗粒浸入培养液后,观察到氟化物立即缓慢释放,氟化物浓度随时间增加,在0.5小时时达到1.25±0.05 ppm F,24小时时达到1.57±0.12 ppm F,48小时时达到1.73±0.15 ppm F。在侵袭试验中,与用未氟化对照样品培养的细胞相比,证实暴露于释放出的氟化物的人成骨样MG - 63细胞发生了迁移(P <.01)。此外,添加到培养基中的氟化物以依赖于氟化物浓度的方式增加了MG - 63细胞的增殖,直至2.0 ppm(P <.05)。然而,在5.0 ppm时,氟化物显著抑制细胞增殖(P <.005)。成骨分化标志物碱性磷酸酶(ALP)的活性在暴露1周后也随氟化物增加,在1.0 ppm时显著增加(P <.05)。MG - 63细胞迁移和增殖的促进以及ALP活性的增加表明,通过用中性4% NaF溶液预先处理而氟化的可吸收HA颗粒表面释放的氟化物可以提供一种极好的方法来供应氟化物并促进成骨细胞分化。