The inhibition of calcium oxalate monohydrate crystal growth by maleic acid copolymers

被引:21
作者
Bouropoulos, K
Bouropoulos, N
Melekos, M
Koutsoukos, PG
Chitanu, GC
Anghelescu-Dogaru, AG
Carpov, AA
机构
[1] Univ Patras, Dept Chem Engn, GR-26500 Patras, Greece
[2] Univ Patras, Sch Med, Dept Urol, GR-26500 Patras, Greece
[3] Inst Chem Engn & High Temp Chem Proc, GR-26110 Patras, Greece
[4] Petru Poni Inst Macromol Chem, R-6600 Iasi, Romania
关键词
calcium oxalate monohydrate; maleic acid copolymers;
D O I
10.1097/00005392-199805000-00107
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
The crystallization of calcium oxalate monohydrate (COM) was investigated at conditions of constant supersaturation both in the absence and in the presence of synthetic maleic acid copolymers at 37C, 0.15 M NaCl. The dependence of the rates of COM crystallization in the absence of inhibitors was found to be second order at low and first order at higher supersaturations suggesting a surface diffusion controlled mechanism. The presence of all copolymers tested at concentration levels up to 5 ppm retarded the rates of COM crystal growth up to 90%. The decrease of the COM crystal growth rates by the polymers depended on the nature of the comonomer polymerized with maleic acid and the order of inhibition was found to be vinyl acetate > N-vinylpyrrolidone > styrene. Taking into consideration kinetics data published in the literature concerning the inhibition of COM crystal growth, it is suggested that molecular weight also plays a role, with more inhibition at higher molecular weights, The morphology of the COM crystals grown was unaffected yet the crystals growing at lower rates in the presence of the copolymers were larger and their size more uniform. It is concluded that maleic acid copolymers are strong inhibitors of the crystallization of COM, the inhibitory activity being more pronounced in the case of the linear copolymers.
引用
收藏
页码:1755 / 1761
页数:7
相关论文
共 41 条
[1]  
AMJAD Z, 1993, LANGMUIR, V9, P5597
[2]   Adsorption-desorption behavior of acrylic-maleic acid copolymer at clay minerals [J].
Blockhaus, F ;
Sequaris, JM ;
Narres, HD ;
Schwuger, MJ .
JOURNAL OF COLLOID AND INTERFACE SCIENCE, 1997, 186 (02) :234-247
[3]   ZETA-POTENTIAL DISTRIBUTION ON CALCIUM-OXALATE CRYSTAL AND TAMM-HORSFALL PROTEIN SURFACE ANALYZED WITH DOPPLER ELECTROPHORETIC LIGHT-SCATTERING [J].
BOEVE, ER ;
CAO, LC ;
DEBRUIJN, WC ;
ROBERTSON, WG ;
ROMIJN, JC ;
SCHRODER, FH .
JOURNAL OF UROLOGY, 1994, 152 (02) :531-536
[4]   A model system for the investigation of urinary stone formation [J].
Bouropoulos, N ;
Bouropoulos, C ;
Klepetsanis, PG ;
Melekos, M ;
Barbalias, G ;
Koutsoukos, PG .
BRITISH JOURNAL OF UROLOGY, 1996, 78 (02) :169-175
[5]   THE DUAL ROLE OF POLY-ELECTROLYTES AND PROTEINS AS MINERALIZATION PROMOTERS AND INHIBITORS OF CALCIUM-OXALATE MONOHYDRATE [J].
CAMPBELL, AA ;
EBRAHIMPOUR, A ;
PEREZ, L ;
SMESKO, SA ;
NANCOLLAS, GH .
CALCIFIED TISSUE INTERNATIONAL, 1989, 45 (02) :122-128
[6]  
CARPOV A, 1979, Patent No. 70120
[7]   CALCIUM OXALATE - CRYSTALLOGRAPHIC ANALYSIS IN SOLID AGGREGATES IN URINARY SEDIMENTS [J].
CATALINA, F ;
CIFUENTES, L .
SCIENCE, 1970, 169 (3941) :183-+
[8]  
CAZE C, 1973, B SOC CHIM FR I-PHYS, P2977
[9]  
CHITANU GC, 1996, Patent No. 0104
[10]  
CHITANU GC, 1997, IN PRESS INT J POLYM