Surface functionalization of 3D glass-ceramic porous scaffolds for enhanced mineralization in vitro

被引:15
作者
Ferraris, Sara [1 ]
Vitale-Brovarone, Chiara [1 ]
Bretcanu, Oana [1 ]
Cassinelli, Clara [2 ]
Verne, Enrica [1 ]
机构
[1] Politecn Torino, Appl Sci & Technol Dept, I-10129 Turin, Italy
[2] NobilBio Ric, Portacomaro At, Asti, Italy
关键词
Surface functionalization; Scaffold; Bone integration; Bioactivity; ALKALINE-PHOSPHATASE; BIOACTIVE GLASS; BIOCHEMICAL MODIFICATION; BONE; STRENGTH; DELIVERY; BINDING;
D O I
10.1016/j.apsusc.2013.02.002
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Bone reconstruction after tissue loosening due to traumatic, pathological or surgical causes is in increasing demand. 3D scaffolds are a widely studied solution for supporting new bone growth. Bioactive glass-ceramic porous materials can offer a three-dimensional structure that is able to chemically bond to bone. The ability to surface modify these devices by grafting biologically active molecules represents a challenge, with the aim of stimulating physiological bone regeneration with both inorganic and organic signals. In this research work glass ceramic scaffolds with very high mechanical properties and moderate bioactivity have been functionalized with the enzyme alkaline phosphatase (ALP). The material surface was activated in order to expose hydroxyl groups. The activated surface was further grafted with ALP both via silanization and also via direct grafting to the surface active hydroxyl groups. Enzymatic activity of grafted samples were measured by means of UV-vis spectroscopy before and after ultrasonic washing in TRIS-HCl buffer solution. In vitro inorganic bioactivity was investigated by soaking the scaffolds after the different steps of functionalization in a simulated body fluid (SBF). SEM observations allowed the monitoring of the scaffold morphology and surface chemical composition after soaking in SBF. The presence of ALP enhanced the in vitro inorganic bioactivity of the tested material. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:412 / 420
页数:9
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