Burguera Elena F, Xu Hockin H K, Weir Michael D
Instituto de Cerámica de Galicia, Universidad de Santiago de Compostela, 15782 Santiago de Compostela, Spain.
J Biomed Mater Res B Appl Biomater. 2006 Apr;77(1):126-34. doi: 10.1002/jbm.b.30403.
Calcium phosphate cement (CPC) sets in situ with intimate adaptation to the contours of defect surfaces, and forms an implant having a structure and composition similar to hydroxyapatite, the putative mineral in teeth and bones. The objective of the present study was to develop an injectable CPC using dicalcium phosphate dihydrate (DCPD) with a high solubility for rapid setting. Two agents were incorporated to impart injectability and fast-hardening to the cement: a hardening accelerator (sodium phosphate) and a gelling agent (hydroxypropyl methylcellulose, HPMC). The cement with DCPD was designated as CPC(D), and the conventional cement was referred to as CPC(A). Using water without sodium phosphate, CPC(A) had a setting time of 82 +/- 6 min. In contrast, CPC(D) exhibited rapid setting with a time of 17 +/- 1 min. At 0.2 mol/L sodium phosphate, setting time for CPC(D) was 15 +/- 1 min, significantly faster than 40 +/- 2 min for CPC(A) (Tukey's at 0.95). Sodium phosphate decreased the paste injectability (measured as the paste mass extruded from the syringe divided by the original paste mass inside the syringe). However, the addition of HPMC dramatically increased the paste injectability. For CPC(D), the injectability was increased from 65% +/- 12% without HPMC to 98% +/- 1% with 1% HPMC. Injectability of CPC(A) was also doubled to 99% +/- 1%. The injectable and rapid-setting CPC(D) possessed flexural strength and elastic modulus values overlapping the reported values for sintered porous hydroxyapatite implants and cancellous bone. In summary, the rapid setting and relatively high strength and elastic modulus of CPC(D) should help the graft to quickly attain strength and geometrical integrity within a short period of time postoperatively. Furthermore, the injectability of CPC(D) may have potential for procedures involving defects with limited accessibility or narrow cavities, when there is a need for precise placement of the paste, and when using minimally invasive surgical techniques.
磷酸钙骨水泥(CPC)在原位凝固,能紧密贴合缺损表面的轮廓,并形成一种结构和成分与羟基磷灰石相似的植入物,羟基磷灰石是牙齿和骨骼中公认的矿物质。本研究的目的是开发一种使用二水磷酸二钙(DCPD)的可注射CPC,其具有高溶解度以实现快速凝固。加入了两种试剂以使骨水泥具有可注射性并快速硬化:一种硬化促进剂(磷酸钠)和一种胶凝剂(羟丙基甲基纤维素,HPMC)。含DCPD的骨水泥被指定为CPC(D),传统骨水泥被称为CPC(A)。使用不含磷酸钠的水时,CPC(A)的凝固时间为82±6分钟。相比之下,CPC(D)表现出快速凝固,时间为17±1分钟。在0.2mol/L磷酸钠时,CPC(D)的凝固时间为15±1分钟,明显快于CPC(A)的40±2分钟(Tukey检验,置信度为0.95)。磷酸钠降低了糊剂的可注射性(以从注射器挤出的糊剂质量除以注射器内原始糊剂质量来衡量)。然而,加入HPMC显著提高了糊剂的可注射性。对于CPC(D),可注射性从不含HPMC时的65%±12%提高到含1%HPMC时的98%±1%。CPC(A)的可注射性也增加了一倍,达到99%±1%。可注射且快速凝固的CPC(D)的抗弯强度和弹性模量值与报道的烧结多孔羟基磷灰石植入物和松质骨的值重叠。总之,CPC(D)的快速凝固以及相对较高的强度和弹性模量应有助于移植物在术后短时间内迅速获得强度和几何完整性。此外,当需要精确放置糊剂以及使用微创手术技术时,对于涉及可及性有限的缺损或狭窄腔隙的手术,CPC(D)的可注射性可能具有潜力。