Department of Prosthetic Dentistry, BIOMAT Research Group, KU Leuven, Leuven, Belgium.
J Clin Periodontol. 2012 Dec;39(12):1206-13. doi: 10.1111/jcpe.12005. Epub 2012 Oct 8.
To evaluate bone regeneration potential of bone morphogenetic protein-2 (BMP-2) adsorbed on amorphous microporous silica (AMS).
MATERIALS & METHODS: Four implants [titanium as control (CTR); AMS-coated titanium (AMS), BMP-2 adsorbed on titanium (CTR+BMP) and AMS (AMS+BMP)] were implanted randomly in the tibiae of 20 New Zealand white rabbits. Bone specimens with implants were retrieved 2/4 weeks post implantation and analysed histologically and histomorphometrically. Bone fraction was measured in initial bone-free area (bone regeneration area, BRA) and in the area with initial bone-implant contact [bone adaptation area (BAA)] (BF(BRA) & BF(BAA) ). Bone-implant contact was measured in BRA (BIC(BRA) ). In vitro BMP-2 release profiles were determined to evaluate the impact of the carrier surface. Mixed models were used for statistical analysis.
BMP-2 release profiles were different for CTR+BMP and AMS+BMP. BIC(BRA) and BF(BRA) were significantly increased after 4 weeks compared to 2 weeks for AMS, CTR+BMP and AMS+BMP. However, no differences between the implant types were observed within both healing periods. BF(BAA) for CTR+BMP was smaller than that for CTR and AMS+BMP after 4 weeks. Despite slower BMP-2 release, AMS+BMP did not stimulate bone regeneration. CTR+BMP caused bone resorption at the bone-implant interface.
BMP-2 functionalized implant surfaces failed to stimulate bone regeneration and osseointegration.
评估吸附在无定形微孔硅(AMS)上的骨形态发生蛋白-2(BMP-2)的骨再生潜力。
将四个植入物[钛作为对照(CTR);AMS 涂层钛(AMS)、钛吸附 BMP-2(CTR+BMP)和 AMS 吸附 BMP-2(AMS+BMP)]随机植入 20 只新西兰白兔的胫骨中。植入后 2/4 周取出带有植入物的骨标本,进行组织学和组织形态计量学分析。在初始无骨区(骨再生区,BRA)和初始骨-植入物接触区[骨适应区(BAA)](BF(BRA)和 BF(BAA))测量骨分数。在 BRA 中测量骨-植入物接触(BIC(BRA))。通过体外 BMP-2 释放曲线评估载体表面的影响。采用混合模型进行统计学分析。
CTR+BMP 和 AMS+BMP 的 BMP-2 释放曲线不同。与 2 周相比,植入后 4 周 AMS、CTR+BMP 和 AMS+BMP 的 BIC(BRA)和 BF(BRA)均显著增加。然而,在两个愈合期内,植入物类型之间没有差异。4 周时,CTR+BMP 的 BF(BAA)小于 CTR 和 AMS+BMP。尽管 BMP-2 释放较慢,但 AMS+BMP 并未刺激骨再生。CTR+BMP 在骨-植入物界面引起了骨吸收。
功能化的 BMP-2 植入物表面未能刺激骨再生和骨整合。