Setting properties and in vitro bioactivity of strontium-enriched gelatin-calcium phosphate bone cements

被引:76
作者
Panzavolta, S. [1 ]
Torricelli, P.
Sturba, L. [1 ]
Bracci, B. [1 ]
Giardino, R. [2 ]
Bigi, A. [1 ]
机构
[1] Univ Bologna, Dept Chem G Ciamician, I-40126 Bologna, Italy
[2] Univ Bologna, Bologna, Italy
关键词
calcium phosphate bone cement; bioactivity; in vitro; biocompatibility; strontium;
D O I
10.1002/jbm.a.31412
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Strontium is known to reduce bone resorption and stimulate bone formation. We have investigated the effect of strontium on the setting properties and in vitro bioactivity of a biomimetic gelatin-calcium phosphate bone cement. Gelatin-alpha-TCP powders, with a gelatin content of 15 wt %, were prepared by grinding and sieving the solid compounds obtained by casting gelatin aqueous solutions containing alpha-TCP. 5 wt % of CaHPO4 center dot 2H(2)O were added to the cement powders before mixing with the liquid phase, with a L/P ratio of 0.3 mL/g. Strontium was added as SrCl2 center dot 6H(2)O in different amounts up to 5 atom %. X-ray diffraction analysis, mechanical tests, and SEM investigations were carried out on the cements after different times of soaking in physiological solution. The presence of strontium affects both the initial and the final setting times of the cements, which increase with the ion content. The microstructural modifications observed in the SEM micrographs of the fractured surfaces are in agreement with the increase of the total porosity, and with the slight reduction of the compressive strength of the aged cements, on increasing strontium content. The rate of transformation of alpha-TCP into calcium deficient hydroxyapatite increases on increasing strontium content. SEM reveals that MG63 osteoblasts grown on the cements show a normal morphology and biological tests demonstrate very good rate of proliferation and viability in every experimental time. In particular, strontium stimulates Alkaline Phosphatase activity, Collagen type 1, osteocalcin, and osteoprotegerin expression. (C) 2007 Wiley Periodicals, Inc.
引用
收藏
页码:965 / 972
页数:8
相关论文
共 34 条
[1]  
Atsushi E, 2003, BIOMATERIALS, V24, P831
[2]   OSTEOBLAST AND CHONDROBLAST DIFFERENTIATION [J].
AUBIN, JE ;
LIU, F ;
MALAVAL, L ;
GUPTA, AK .
BONE, 1995, 17 (02) :S77-S83
[3]   Effect of porosity reduction by compaction on compressive strength and microstructure of calcium phosphate cement [J].
Barralet, JE ;
Gaunt, T ;
Wright, AJ ;
Gibson, IR ;
Knowles, JC .
JOURNAL OF BIOMEDICAL MATERIALS RESEARCH, 2002, 63 (01) :1-9
[4]   Normal and osteopenic bone-derived osteoblast response to a biomimetic gelatin-calcium phosphate bone cement [J].
Bigi, A. ;
Panzavolta, S. ;
Sturba, L. ;
Torricelli, P. ;
Fini, M. ;
Giardino, R. .
JOURNAL OF BIOMEDICAL MATERIALS RESEARCH PART A, 2006, 78A (04) :739-745
[5]   A biomimetic gelatin-calcium phosphate bone cement [J].
Bigi, A ;
Torricelli, P ;
Fini, M ;
Bracci, B ;
Panzavolta, S ;
Sturba, L ;
Giardino, R .
INTERNATIONAL JOURNAL OF ARTIFICIAL ORGANS, 2004, 27 (08) :664-673
[6]   Setting mechanism of a biomimetic bone cement [J].
Bigi, A ;
Panzavolta, S ;
Rubini, K .
CHEMISTRY OF MATERIALS, 2004, 16 (19) :3740-3745
[7]   Effect of added gelatin on the properties of calcium phosphate cement [J].
Bigi, A ;
Bracci, B ;
Panzavolta, S .
BIOMATERIALS, 2004, 25 (14) :2893-2899
[8]   α-Tricalcium phosphate hydrolysis to octacalcium phosphate:: effect of sodium polyacrylate [J].
Bigi, A ;
Boanini, E ;
Botter, R ;
Panzavolta, S ;
Rubini, K .
BIOMATERIALS, 2002, 23 (08) :1849-1854
[9]   SR-89 THERAPY - STRONTIUM KINETICS IN DISSEMINATED CARCINOMA OF THE PROSTATE [J].
BLAKE, GM ;
ZIVANOVIC, MA ;
MCEWAN, AJ ;
ACKERY, DM .
EUROPEAN JOURNAL OF NUCLEAR MEDICINE, 1986, 12 (09) :447-454
[10]  
BONHER M, 2000, INJURY, V31, pD37