In vitro characterization of peptide-modified p(AAm-co-EG/AAc) IPN-coated titanium implants

被引:33
作者
Barber, Thomas A.
Gamble, Lara J.
Castner, David G.
Healy, Kevin E. [1 ]
机构
[1] Univ Calif Berkeley, Dept Bioengn, Berkeley, CA 94720 USA
[2] Univ Washington, Dept Bioengn, Natl ESCA & Surface Anal Ctr Biomed Problems, Seattle, WA 98195 USA
[3] Univ Washington, Dept Chem, Natl ESCA & Surface Anal Ctr Biomed Problems, Seattle, WA 98195 USA
[4] Univ Calif Berkeley, Dept Mat Sci & Engn, Berkeley, CA 94720 USA
关键词
titanium implant; RGD; PEG; IPN; osteoblast;
D O I
10.1002/jor.20165
中图分类号
R826.8 [整形外科学]; R782.2 [口腔颌面部整形外科学]; R726.2 [小儿整形外科学]; R62 [整形外科学(修复外科学)];
学科分类号
摘要
Interpenetrating polymer networks (IPNs) of poly(acrylamide-co-ethylene glycol/ acrylic acid) [p(AAm-co-EG/AAc)] functionalized with an -Arg-Gly-Asp- containing peptide derived from rat bone sialoprotein [bsp-RGD(15)] were grafted to titanium implants in an effort to modulate osteoblast behavior in vitro. Surface characterization data were consistent with the presence of an IPN, and ligand density measurements established that the range of peptide density on the modified implants spanned three orders of magnitude (0. 0 1-20 pmol/cm(2)). In vitro biological characterization of the modified implants employing the primary rat calvarial osteoblast (RCO) model resulted in the identification of a critical ligand density (0. 0 1 < Gamma(crit) < 0. 1 pmol/cm(2)) for maximal support of the osteoblast phenotype. After 14 and 21 days, mineralization was greater on the 0.1 and 10 pmol/cm(2) bsp-RGD(15) modified implants compared to the base titanium and other control surfaces. The observed effects were attributed to specific interactions with bsp-RGD(15) and support the concept that peptide-modified implants can enhance the kinetics of differentiation of the cells they contact. These results suggest that in vivo biological performance evaluation of these biomimetic implant surfaces is merited. (c) 2006 Orthopaedic Research Society.Published by Wiley Periodicals, Inc.
引用
收藏
页码:1366 / 1376
页数:11
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