Nacre surface transformation to hydroxyapatite in a phosphate buffer solution

被引:122
作者
Ni, M
Ratner, BD
机构
[1] Univ Washington, Dept Chem Engn, UWEB, Seattle, WA 98195 USA
[2] Univ Washington, Dept Bioengn, UWEB, Seattle, WA 98195 USA
关键词
nacre; aragonite; hydroxyapatite; X-ray photoelectron spectroscopy; secondary ion mass spectroscopy; Fourier transform infrared spectroscopy; scanning electron microscopy;
D O I
10.1016/S0142-9612(03)00236-9
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Nacre. also known as mother-of-pearl, constitutes the inner layer of mollusc shells. Nacre is a natural composite material consisting mostly of calcium carbonate in the aragonite crystal form and some organic matter. Previous studies have shown that geological aragonite, coral and nacre can convert hydrothermally to hydroxyapatite (HAP) in phosphate solution by a solid-state topotactic ion-exchange reaction. This conversion typically occurs within the range of 140-260degreesC, although higher temperatures are possible. In this work, we have found that nacre can transform to HAP in a phosphate buffer solution at room temperature via a surface reaction. The morphology of the nacre-transformed HAP surface was investigated by scanning electron microscopy (SEM). The HAP surfaces were characterized by X-ray photoelectron spectroscopy (XPS) and secondary ion mass spectroscopy (SIMS). A layer covered with packed particles was found in contrast to the tablet structure typical of nacre surfaces. XPS and SIMS indicated that the mineral phase of the nacre surface had converted from an aragonite phase to an HAP phase. Fourier transform infrared spectroscopy (FTIR) showed that phosphate (PO4) bands appeared after nacre was soaked in a phosphate buffer and the intensity of the PO4 bands increased with exposure time. The FTIR was consistent with XPS and SIMS results. We suggest that this surface reaction occurs by a dissolution-precipitation mechanism. Calcium ions are released from the nacre surface, react with phosphate ions in the buffer solution, and then precipitate as HAP on the nacre surface. (C) 2003 Elsevier Ltd. All rights reserved.
引用
收藏
页码:4323 / 4331
页数:9
相关论文
共 48 条
[11]   Calcium phosphate phase identification using XPS and time-of-flight cluster SIMS [J].
Chusuei, CC ;
Goodman, DW ;
Van Stipdonk, MJ ;
Justes, DR ;
Schweikert, EA .
ANALYTICAL CHEMISTRY, 1999, 71 (01) :149-153
[12]   REACTIONS BETWEEN SOLID CALCIUM CARBONATE AND ORTHOPHOSPHATE SOLUTIONS [J].
CLARK, JS ;
TURNER, RC .
CANADIAN JOURNAL OF CHEMISTRY-REVUE CANADIENNE DE CHIMIE, 1955, 33 (04) :665-671
[13]  
Digby P. S., 1968, Symposia of the Zoological Society of London, VNo. 22, P93
[14]  
DOWNES S, 1991, BONE BONDING BIOMATE, P101
[15]   BIOACTIVE MATERIAL TEMPLATE FOR IN-VITRO SYNTHESIS OF BONE [J].
ELGHANNAM, A ;
DUCHEYNE, P ;
SHAPIRO, IM .
JOURNAL OF BIOMEDICAL MATERIALS RESEARCH, 1995, 29 (03) :359-370
[16]  
ELLIOTT JC, 1994, STRUCTURE CHEM APATI, P6
[17]   TOPOTACTIC REACTION OF ARAGONITE TO HYDROXYAPATITE [J].
EYSEL, W ;
ROY, DM .
ZEITSCHRIFT FUR KRISTALLOGRAPHIE, 1975, 141 (1-2) :11-24
[18]   Polymorph and morphology of calcium carbonate crystals induced by proteins extracted from mollusk shell [J].
Feng, QL ;
Pu, G ;
Pei, Y ;
Cui, FZ ;
Li, HD ;
Kim, TN .
JOURNAL OF CRYSTAL GROWTH, 2000, 216 (1-4) :459-465
[19]  
GEER DE, 1972, J WATER POLLUT CON F, V44, P2342
[20]  
Hench L.L., 1971, Journal of Biomedical Materials Research Symposium, V36, P117, DOI DOI 10.1002/JBM.820050611