Use of dicalcium phosphate dihydrate as a probe in an approach for accurate calculations of solution equilibria in buffered calcium phosphate systems

被引:13
作者
Chhettry, A [1 ]
Wang, ZR [1 ]
Fox, JL [1 ]
Baig, AA [1 ]
Zhuang, H [1 ]
Higuchi, WI [1 ]
机构
[1] Univ Utah, Dept Pharmaceut & Pharmaceut Chem, Salt Lake City, UT 84112 USA
关键词
calcium phosphates; solubility; stability constants;
D O I
10.1006/jcis.1999.6307
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Both synthetic and biological carbonated apatites have been shown to possess metastable equilibrium solubility (MES) distributions. Investigation of their MES behavior requires accurate knowledge of the activities of the relevant ions over a range of solution compositions. This in turn requires that the activity coefficients for these ions and the stability constants for the various solution complexes be accurately known. Since the solubility of dicalcium phosphate dihydrate (DCPD) can be easily determined, it can be used as a probe to study the appropriateness of proposed sets of stability constants and activity coefficients. In the present study, the solubility of DCPD was determined in acetate buffer solutions at pHs ranging from 4.5 to 6.5 and this allowed for the determination and evaluation of the stability constants of the NaHPO4-, CaHPO40, CaH2PO4+, and CaAc+ complexes. The activity coefficients were calculated by a modification of the extended Debye-Huckel method and also by Bockris and Reddy's method, in which the activity of water and the hydration numbers of ions are also considered. The solution conditions were controlled to simulate the dissolution media used for the determination of MES distributions of apatites in our laboratory. Both methods of activity coefficient determination gave very consistent DCPD solubility product (K-DCPD) values, and values for the stability constants of the relevant complexes determined using the two methods were close to each other. This approach of determining the stability constants under a set of conditions similar to those in apatite dissolution studies offers an effective set of parameters which, though not necessarily always exactly correct in absolute terms, are internally consistent and should allow for the quantitative characterization of the MES behavior of apatites. (C) 1999 Academic Press.
引用
收藏
页码:47 / 56
页数:10
相关论文
共 44 条
[1]   1ST DISSOCIATION CONSTANT OF PHOSPHORIC ACID FROM 0-DEGREES-C TO 60-DEGREES-C - LIMITATIONS OF THE ELECTROMOTIVE FORCE METHOD FOR MODERATELY STRONG ACIDS [J].
BATES, RG .
JOURNAL OF RESEARCH OF THE NATIONAL BUREAU OF STANDARDS, 1951, 47 (03) :127-134
[2]   PH OF AQUEOUS MIXTURES OF POTASSIUM DIHYDROGEN PHOSPHATE AND DISODIUM HYDROGEN PHOSPHATE AT 0-DEGREES TO 60-DEGREES-C [J].
BATES, RG ;
ACREE, SF .
JOURNAL OF RESEARCH OF THE NATIONAL BUREAU OF STANDARDS, 1945, 34 (04) :373-394
[3]  
BILTZ RM, 1970, J CLIN ORTHOP, V71, P219
[4]  
BJERRUM N, 1929, KGL DANSKE VIDENSK S, V9, P5
[5]  
Bockris J. O. M., 1970, MODERN ELECTROCHEMIS
[6]   FORMATION OF CAHPO4 2H2O FROM ENAMEL MINERAL AND ITS RELATIONSHIP TO CARIES MECHANISM [J].
BROWN, WE ;
PATEL, PR ;
CHOW, LC .
JOURNAL OF DENTAL RESEARCH, 1975, 54 (03) :475-481
[7]  
Butler J. N., 1982, CARBON DIOXIDE EQUIL
[8]  
CHHETTRY A, IN PRESS J COLLOID I
[9]   COMPLEXES IN CALCIUM PHOSPHATE SOLUTIONS [J].
CHUGHTAI, A ;
MARSHALL, R ;
NANCOLLAS, GH .
JOURNAL OF PHYSICAL CHEMISTRY, 1968, 72 (01) :208-+
[10]   ON THE POSSIBILITY OF DETERMINING THE THERMODYNAMIC PARAMETERS FOR THE FORMATION OF WEAK COMPLEXES USING A SIMPLE-MODEL FOR THE DEPENDENCE ON IONIC-STRENGTH OF ACTIVITY-COEFFICIENTS - NA+, K+, AND CA-2+ COMPLEXES OF LOW-MOLECULAR WEIGHT LIGANDS IN AQUEOUS-SOLUTION [J].
DANIELE, PG ;
DEROBERTIS, A ;
DESTEFANO, C ;
SAMMARTANO, S ;
RIGANO, C .
JOURNAL OF THE CHEMICAL SOCIETY-DALTON TRANSACTIONS, 1985, (11) :2353-2361