Department of Orthopedics and Traumatology, Lithuanian University of Health Sciences, Kaunas, Lithuania; The Faculty of Medicine, Department of Clinical Sciences Lund, Orthopedics, Lund University, Lund, Sweden.
The Faculty of Medicine, Division of Dermatology and Venerology, Lund University, 221 84 Lund, Sweden.
Acta Biomater. 2024 Apr 15;179:354-370. doi: 10.1016/j.actbio.2024.03.005. Epub 2024 Mar 13.
Fracture fixation in an ageing population is challenging and fixation failure increases mortality and societal costs. We report a novel fracture fixation treatment by applying a hydroxyapatite (HA) based biomaterial at the bone-implant interface and biologically activating the biomaterial by systemic administration of a bisphosphonate (zoledronic acid, ZA). We first used an animal model of implant integration and applied a calcium sulphate (CaS)/HA biomaterial around a metallic screw in the tibia of osteoporotic rats. Using systemic ZA administration at 2-weeks post-surgery, we demonstrated that the implant surrounded by HA particles showed significantly higher peri‑implant bone formation compared to the unaugmented implants at 6-weeks. We then evaluated the optimal timing (day 1, 3, 7 and 14) of ZA administration to achieve a robust effect on peri‑implant bone formation. Using fluorescent ZA, we demonstrated that the uptake of ZA in the CaS/HA material was the highest at 3- and 7-days post-implantation and the uptake kinetics had a profound effect on the eventual peri‑implant bone formation. We furthered our concept in a feasibility study on trochanteric fracture patients randomized to either CaS/HA augmentation or no augmentation followed by systemic ZA treatment. Radiographically, the CaS/HA group showed signs of increased peri‑implant bone formation compared with the controls. Finally, apart from HA, we demonstrated that the concept of biologically activating a ceramic material by ZA could also be applied to β-tricalcium phosphate. This novel approach for fracture treatment that enhances immediate and long-term fracture fixation in osteoporotic bone could potentially reduce reoperations, morbidity and mortality. STATEMENT OF SIGNIFICANCE: • Fracture fixation in an ageing population is challenging. Biomaterial-based augmentation of fracture fixation devices has been attempted but lack of satisfactory biological response limits their widespread use. • We report the biological activation of locally implanted microparticulate hydroxyapatite (HA) particles placed around an implant by systemic administration of the bisphosphonate zoledronic acid (ZA). The biological activation of HA by ZA enhances peri‑implant bone formation. •Timing of ZA administration after HA implantation is critical for optimal ZA uptake and consequently determines the extent of peri‑implant bone formation. • We translate the developed concept from small animal models of implant integration to a proof-of-concept clinical study on osteoporotic trochanteric fracture patients. • ZA based biological activation can also be applied to other calcium phosphate biomaterials.
在老龄化人口中,骨折固定具有挑战性,且固定失败会增加死亡率和社会成本。我们报告了一种新的骨折固定治疗方法,即在骨-植入物界面应用羟基磷灰石(HA)基生物材料,并通过全身给予双膦酸盐(唑来膦酸,ZA)来生物激活该生物材料。我们首先使用植入物整合的动物模型,并在骨质疏松大鼠的胫骨中用硫酸钙(CaS)/HA 生物材料围绕金属螺钉应用。在手术后 2 周进行全身 ZA 给药,我们证明与未增强的植入物相比,被 HA 颗粒包围的植入物在 6 周时表现出明显更高的植入物周围骨形成。然后,我们评估了 ZA 给药的最佳时机(第 1、3、7 和 14 天),以实现对植入物周围骨形成的强大作用。使用荧光 ZA,我们证明在植入后 3-7 天,ZA 在 CaS/HA 材料中的摄取量最高,摄取动力学对最终植入物周围骨形成有深远影响。我们在一项关于随机分为 CaS/HA 增强或不增强后接受全身 ZA 治疗的转子间骨折患者的可行性研究中进一步推进了我们的概念。放射学上,与对照组相比,CaS/HA 组显示出增加的植入物周围骨形成迹象。最后,除了 HA,我们还证明了通过 ZA 生物激活陶瓷材料的概念也可以应用于β-磷酸三钙。这种增强骨质疏松性骨折即时和长期固定的新型骨折治疗方法可能会减少再次手术、发病率和死亡率。 意义声明: • 在老龄化人口中,骨折固定具有挑战性。已经尝试了基于生物材料的骨折固定装置增强,但缺乏令人满意的生物学反应限制了它们的广泛使用。 • 我们报告了通过全身给予双膦酸盐唑来膦酸(ZA)来生物激活局部植入的微颗粒羟基磷灰石(HA)颗粒周围的植入物。ZA 对 HA 的生物激活增强了植入物周围的骨形成。 • ZA 给药后 HA 植入的时间对于最佳 ZA 摄取至关重要,进而决定了植入物周围骨形成的程度。 • 我们将从小鼠植入物整合模型中开发的概念转化为骨质疏松性转子间骨折患者的概念验证临床研究。 • ZA 基生物激活也可应用于其他磷酸钙生物材料。