Greish Yaser E, Brown Paul W
Materials Research Institute, The Pennsylvania State University, University Park, Pennsylvania 16802, USA.
J Biomed Mater Res B Appl Biomater. 2003 Oct 15;67(1):632-7. doi: 10.1002/jbm.b.10056.
The mechanism of formation of stoichiometric hydroxyapatite in aqueous solution by the acid-base reaction of the precursor calcium phosphates tetracalcium phosphate [Ca4(PO4)2O, TetCP] and anhydrous dicalcium phosphate (CaHPO4, DCPA) was investigated. Phase evolution during the formation of hydroxyapatite was studied, and could be correlated with the kinetics of reaction. Initial dissolution of precursors is followed by hydroxyapatite nucleation and growth. Consumption of DCPA precedes that of TetCP and results in the formation of nonstoichiometric hydroxyapatite. As a result of continued TetCP dissolution, the pH of the solution increases towards a pH at which hydroxyapatite and Ca(OH)2 co-exist in equilibrium. Hydroxyapatite formation takes place in two stages: initially formed, nonstoichiometric hydroxyapatite subsequently reacts with TetCP and is converted to stoichiometric hydroxyapatite.
通过前体磷酸钙磷酸四钙[Ca4(PO4)2O,TetCP]和无水磷酸二钙(CaHPO4,DCPA)的酸碱反应在水溶液中形成化学计量比羟基磷灰石的机制进行了研究。研究了羟基磷灰石形成过程中的相演变,并将其与反应动力学相关联。前体的初始溶解之后是羟基磷灰石的成核和生长。DCPA的消耗先于TetCP的消耗,并导致形成非化学计量比的羟基磷灰石。由于TetCP的持续溶解,溶液的pH值朝着羟基磷灰石和Ca(OH)2平衡共存的pH值增加。羟基磷灰石的形成分两个阶段进行:最初形成的非化学计量比羟基磷灰石随后与TetCP反应并转化为化学计量比的羟基磷灰石。