Removal of surface by-products from sintered hydroxyapatite: Effect of a chelation treatment on fibronectin adsorption and cell adhesion

被引:9
作者
Pellenc, D
Giraudier, S
Champion, E
Anselme, K
Larreta-Garde, V
Gallet, O [1 ]
机构
[1] Univ Cergy Pontoise, ERRMECe, Pontoise, France
[2] Univ Limoges, CNRS, UMR 6638, SPCTS, Limoges, France
[3] CNRS, UPR 9069, ICSI, Mulhouse, France
关键词
calcium phosphates; surface treatment; cell adhesion; fibronectin; EDTA;
D O I
10.1002/jbm.b.30352
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
It was observed that fibronectin precipitates when deposited on hydroxyapatitel (HA) ceramics. Fibronectin's known affinity for calcium and the composition of the ceramic itself suggested that calcium release could be the main cause of this aggregation effect. It was then decided to investigate the effect of a surface chelation treatment on fibronectin adsorption, and MG63 cell adhesion, onto porous ceramics of hydroxyapatite (HA), beta-tricalcium phosphate (beta-TCP), and HA/TCP biphasic material (BCP). Those ceramics were immersed in an EDTA solution and the effect of this treatment on the material composition was assayed. X-ray diffraction data showed the presence of alpha- and beta-TCP phases in HA and BCP materials, which were both completely removed by the chelation treatment in the case of HA. On BCP, a-TCP was removed and beta-TCP partially dissolved. The TCP material, which was pure beta-TCP, underwent a mass loss, but no change in composition was observed. Adhesion of MG63 cells was overall higher on the fibronectin-coated EDTA-treated HA material, but was especially enhanced on EDTA-treated HA. Changes in surface morphologies, as compared with the use of scanning electron microscopy, did not seem to be related to the effects observed. The EDTA treatment proved to be a very efficient way of removing by-products of HA sintered materials, and thus enhancing the biocompatibility of the material. (c) 2005 Wiley Periodicals, Inc.
引用
收藏
页码:136 / 142
页数:7
相关论文
共 47 条
[21]   Resorbable bioceramics based on stabilized calcium phosphates. Part I: rational design, sample preparation and material characterization [J].
Langstaff, S ;
Sayer, M ;
Smith, TJN ;
Pugh, SM ;
Hesp, SAM ;
Thompson, WT .
BIOMATERIALS, 1999, 20 (18) :1727-1741
[22]   Resorbable bioceramics based on stabilized calcium phosphates. Part II: evaluation of biological response [J].
Langstaff, S ;
Sayer, M ;
Smith, TJN ;
Pugh, SM .
BIOMATERIALS, 2001, 22 (02) :135-150
[23]   Petal-like apatite formed on the surface of tricalcium phosphate ceramic after soaking in distilled water [J].
Lin, FH ;
Liao, CJ ;
Chen, KS ;
Sun, JS ;
Lin, CP .
BIOMATERIALS, 2001, 22 (22) :2981-2992
[24]   Role of interconnections in porous bioceramics on bone recolonization in vitro and in vivo [J].
Lu, JX ;
Flautre, B ;
Anselme, K ;
Hardouin, P ;
Gallur, A ;
Descamps, M ;
Thierry, B .
JOURNAL OF MATERIALS SCIENCE-MATERIALS IN MEDICINE, 1999, 10 (02) :111-120
[25]   Diverse mechanisms of osteoblast spreading on hydroxyapatite and titanium [J].
Matsuura, T ;
Hosokawa, R ;
Okamoto, K ;
Kimoto, T ;
Akagawa, Y .
BIOMATERIALS, 2000, 21 (11) :1121-1127
[26]  
McFarland CD, 1999, J BIOMED MATER RES, V44, P1
[27]   Intraindividual comparative animal study of α- and β-tricalcium phosphate degradation in conjunction with simultaneous insertion of dental implants [J].
Merten, HA ;
Wiltfang, J ;
Grohmann, U ;
Hoenig, JF .
JOURNAL OF CRANIOFACIAL SURGERY, 2001, 12 (01) :59-68
[28]  
Moursi AM, 1997, J CELL SCI, V110, P2187
[29]  
Moursi AM, 1996, J CELL SCI, V109, P1369
[30]   Characterization of calcium phosphate phases obtained during the preparation of sintered biphase Ca-P ceramics [J].
Petrov, OE ;
Dyulgerova, E ;
Petrov, L ;
Popova, R .
MATERIALS LETTERS, 2001, 48 (3-4) :162-167