ORGANOAPATITES - MATERIALS FOR ARTIFICIAL BONE .1. SYNTHESIS AND MICROSTRUCTURE

被引:144
作者
STUPP, SI
CIEGLER, GW
机构
[1] Department of Materials Science and Engineering, University of Illinois at Urbana-Champaign, Urbana, Illinois
来源
JOURNAL OF BIOMEDICAL MATERIALS RESEARCH | 1992年 / 26卷 / 02期
关键词
D O I
10.1002/jbm.820260204
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
We have synthesized a new family of materials we termed organoapatites which may be useful in the formulation of artificial bone. These materials are synthesized by nucleation and growth of apatite crystals in media containing poly(amino acids) or synthetic organic polyelectrolytes using strict atmospheric, temperature, and pH control. The macromolecules used to synthesize the organoapatites include poly(L-lysine), poly(L-glutamic acid), and poly(sodium acrylate). The products were characterized by x-ray diffraction, scanning electron microscopy, surface area measurements, elemental analysis, and spectroscopic techniques. Organoapatites were found to contain large surface area morphologies with small crystallites which mature slowly based on analysis of Ca/P ratios. The organic macromolecules are thought to induce nucleation of crystals but also to quench their growth, thus becoming intimately dispersed in a mineral network. The organomineral particles harvested from the reaction medium contain polymer-netted microcrystals, and for this reason the synthetic approach can be used to modulate crystal maturation and biological response. It is likely that the preparative approach mimics some aspects of natural bone matrix synthesis and could be specially useful in the preparation of mineral implants containing intimate dispersions of small amounts of biomolecules such as growth factors, special drugs, or bioadhesives.
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页码:169 / 183
页数:15
相关论文
共 29 条
[1]   INHIBITION OF APATITE CRYSTAL-GROWTH BY THE AMINO-TERMINAL SEGMENT OF HUMAN SALIVARY ACIDIC PROLINE-RICH PROTEINS [J].
AOBA, T ;
MORENO, EC ;
HAY, DI .
CALCIFIED TISSUE INTERNATIONAL, 1984, 36 (06) :651-658
[2]   CHROMATOGRAPHY OF POLYPEPTIDES AND PROTEINS ON HYDROXYAPATITE COLUMNS [J].
BERNARDI, G ;
KAWASAKI, T .
BIOCHIMICA ET BIOPHYSICA ACTA, 1968, 160 (03) :301-&
[3]  
Betts F., 1974, T AM CRYST ASS, V10, P73
[4]   NUCLEOTIDE STABILIZATION OF AMORPHOUS CALCIUM-PHOSPHATE [J].
BLUMENTHAL, NC ;
BETTS, F ;
POSNER, AS .
MATERIALS RESEARCH BULLETIN, 1975, 10 (10) :1055-1060
[5]   CRYSTALLOGRAPHIC AND CHEMICAL RELATIONS BETWEEN OCTACALCIUM PHOSPHATE AND HYDROXYAPATITE [J].
BROWN, WE ;
SMITH, JP ;
FRAZIER, AW ;
LEHR, JR .
NATURE, 1962, 196 (4859) :1050-+
[6]  
BROWN WE, 1966, CLIN ORTHOP, V44
[7]  
CHRISTOFFERSEN MR, 1984, CALCIFIED TISSUE INT, V36, P659, DOI 10.1007/BF02405386
[8]  
CIEGLER GW, 1985, 11TH T ANN M SOC BIO, V8, P165
[9]   KINETICS AND MECHANISM OF CONVERSION OF NONCRYSTALLINE CALCIUM PHOSPHATE TO CRYSTALLINE HYDROXYAPATITE [J].
EANES, ED ;
POSNER, AS .
TRANSACTIONS OF THE NEW YORK ACADEMY OF SCIENCES, 1965, 28 (02) :233-+
[10]   INTERMEDIATE STATES IN PRECIPITATION OF HYDROXYAPATITE [J].
EANES, ED ;
GILLESSE.IH ;
GOSNER, AS .
NATURE, 1965, 208 (5008) :365-+