Paul Scherrer Institut (PSI), ENE, CH-5232 Villigen PSI, Switzerland; École Polytechnique Fédérale de Lausanne (EPFL), ENAC IIS GR-LUD, CH-1015 Lausanne, Switzerland.
Paul Scherrer Institut (PSI), SYN, CH-5232 Villigen PSI, Switzerland.
Acta Biomater. 2018 Jul 1;74:478-488. doi: 10.1016/j.actbio.2018.05.027. Epub 2018 May 18.
The experimental data on calcium phosphates formation were collected in dilute solution at constant pH (7.40) and temperature (37.0 °C) at different levels of ionic strength (IS). The evolution of the solid phase formation is described in detail using a thermodynamic-kinetic model. The thermodynamic model takes into account all relevant chemical species as well as Posner's clusters; the kinetic model, based on the discretized population balance approach, accounts for the solid formation from solution. The experimental data are consistent with an initial formation of dicalcium phosphate dihydrate (DCPD, brushite), which dominates the nucleation rate, and its rapid transformation into octacalcium phosphate (OCP) or hydroxyapatite (HA), which dominates the growth rate. Depending on the experimental conditions and, including the influence of the IS level, OCP may be further transformed into apatite. The classical nucleation theory is able to describe the experimental results very well and the solid phase growth is limited by the diffusion of Ca ions. The precipitation pathway described by a complete thermodynamic-kinetic model is expected to contribute to the understating of the in vivo osteogenesis.
The formation mechanism of calcium phosphates under biomimetic conditions is unraveled. The formation pathway is mathematically described based on a thermodynamic-kinetic model in which (i) the nucleation stages (primary and secondary) are dominated by the formation of dicalcium phosphate dihydrate (DCPD) and (ii) the fast growth stage is limited by the diffusion of Ca ions under the driving force of octacalcium phosphate (OCP), or hydroxyapatite (HA), solubility. The obtained solid phase seems correlated to the activity coefficient of phosphate ions, thus to the ionic strength and local phosphate speciation. The model, being able to highlight the details of the precipitation pathway, is expected to contribute to the understanding of the apatitic phase formation in the biomineralization-biodemineralization processes under in-vivo conditions.
在不同离子强度 (IS) 水平下,于恒定 pH(7.40)和温度 (37.0°C) 的稀溶液中收集钙磷化合物形成的实验数据。使用热力学-动力学模型详细描述了固相形成的演化。热力学模型考虑了所有相关的化学物质以及 Posner 团簇;动力学模型基于离散化的种群平衡方法,从溶液中考虑固相的形成。实验数据与二水合磷酸氢钙(DCPD,磷石膏)的初始形成一致,该相主导着成核速率,并且其迅速转化为八钙磷酸盐(OCP)或羟磷灰石(HA),该相主导着生长速率。取决于实验条件,包括 IS 水平的影响,OCP 可能进一步转化为磷灰石。经典成核理论能够很好地描述实验结果,固相生长受 Ca 离子扩散的限制。完整的热力学-动力学模型描述的沉淀途径有望有助于理解体内成骨作用。
揭示了仿生条件下钙磷化合物的形成机制。基于热力学-动力学模型,以数学方式描述了形成途径,其中(i)成核阶段(一级和二级)主要由二水合磷酸氢钙(DCPD)的形成主导,(ii)快速生长阶段受 Ca 离子扩散的限制,驱动力为八钙磷酸盐(OCP)或羟磷灰石(HA)的溶解度。获得的固相似乎与磷酸根离子的活度系数相关,因此与离子强度和局部磷酸盐形态有关。该模型能够突出沉淀途径的细节,有望有助于理解体内生物矿化-生物脱矿化过程中磷灰石相的形成。