Department of Orthopaedic Surgery, Tohoku University School of Medicine, Sendai 980-8574, Japan; Division of Craniofacial Function Engineering, Tohoku University Graduate School of Dentistry, Sendai 980-8575, Japan.
Acta Biomater. 2014 Jan;10(1):531-43. doi: 10.1016/j.actbio.2013.09.005. Epub 2013 Sep 12.
The present study was designed to investigate whether three sodium hyaluronic acid (HyA) medical products, Artz(®), Suvenyl(®) and a chemically modified derivative of sodium HyA Synvisc(®), can be used as suitable vehicles for an osteoconductive octacalcium phosphate (OCP). OCP granules (300-500 μm diameter) were mixed with these sodium HyAs with molecular weights of 90 × 10(4) (Artz(®)), 190 × 10(4) (Suvenyl(®)) and 600 × 10(4) (Synvisc(®)) (referred to as HyA90, HyA190 and HyA600, respectively). OCP-HyA composites were injected using a syringe into a polytetrafluoroethylene ring, placed on the subperiosteal region of mouse calvaria for 3 and 6 weeks, and then bone formation was assessed by histomorphometry. The capacity of the HyAs for osteoclast formation from RAW264 cells with RANKL was examined by TRAP staining in vitro. Bone formation was enhanced by the OCP composites with HyA90 and HyA600, compared to OCP alone, through enhanced osteoclastic resorption of OCP. HyA90 and HyA600 facilitated in vitro osteoclast formation. The results suggest that the osteoconductive property of OCP was accelerated by the HyAs-associated osteoclastic resorption of OCP, and therefore that HyA/OCP composites are attractive bone substitutes which are injectable and bioactive materials.
本研究旨在探讨三种透明质酸钠(HyA)医学产品,即 Artz(®)、Suvenyl(®)和一种化学修饰的透明质酸钠衍生物 Synvisc(®),是否可用作具有骨诱导性的磷酸八钙(OCP)的合适载体。将直径为 300-500μm 的 OCP 颗粒与分子量分别为 90×10(4)(Artz(®))、190×10(4)(Suvenyl(®))和 600×10(4)(Synvisc(®))的透明质酸钠(HyA90、HyA190 和 HyA600)混合。OCP-HyA 复合材料通过注射器注入聚四氟乙烯环中,置于小鼠颅骨骨膜下区 3 周和 6 周,然后通过组织形态计量学评估骨形成。通过体外 RANKL 诱导 RAW264 细胞形成破骨细胞的 TRAP 染色,检测 HyAs 促进破骨细胞形成的能力。与单独的 OCP 相比,OCP 复合材料与 HyA90 和 HyA600 结合后,通过增强 OCP 的破骨细胞吸收,增强了骨形成。HyA90 和 HyA600 促进了体外破骨细胞的形成。结果表明,OCP 的骨诱导性通过 HyA 相关的 OCP 破骨细胞吸收而加速,因此 HyA/OCP 复合材料是具有吸引力的可注射和生物活性骨替代物。