Increased osteoblast functions on nanophase titania dispersed in poly-lactic-co-glycolic acid composites

被引:48
作者
Liu, HN
Slamovich, EB
Webster, TJ
机构
[1] Purdue Univ, Weldon Sch Biomed Engn, W Lafayette, IN 47907 USA
[2] Purdue Univ, Sch Mat Engn, W Lafayette, IN 47907 USA
关键词
D O I
10.1088/0957-4484/16/7/038
中图分类号
TB3 [工程材料学];
学科分类号
0805 [材料科学与工程]; 080502 [材料学];
摘要
The design of nanophase titania/poly-lactic-co-glycolic acid (PLGA) composites offers an exciting approach to combine the advantages of a degradable polymer with nano-size ceramic grains to optimize physical and biological properties for bone regeneration. Importantly, nanophase titania mimics the size scale of constituent components of bone since it is a nanostructured composite composed of nanometre dimensioned hydroxyapatite well dispersed in a mostly collagen matrix. For these reasons, the objective of the present in vitro study was to investigate osteoblast (bone-forming cell) adhesion and long-term functions on nanophase titania/PLGA composites. Since nanophase titania tended to significantly agglomerate when added to polymers, different sonication output powers were applied in this study to improve titania dispersion. Results demonstrated that the dispersion of titania in PLGA was enhanced by increasing the intensity of sonication and that greater osteoblast adhesion correlated with improved nanophase titania dispersion in PLGA. Moreover, results correlated better osteoblast long-term functions, such as alkaline phosphatase activity and calcium-containing mineral deposition, on nanophase titania/PLGA composites compared to plain PLGA. In fact, the greatest collagen production by osteoblasts occurred when cultured on nanophase titania sonicated in PLGA at the highest powers. In this manner, the present study demonstrates that PLGA composites with well dispersed nanophase titania can enhance osteoblast functions necessary for improved bone tissue engineering applications.
引用
收藏
页码:S601 / S608
页数:8
相关论文
共 30 条
[1]
In vitro evaluation of novel bioactive composites based on Bioglass®-filled polylactide foams for bone tissue engineering scaffolds [J].
Blaker, JJ ;
Gough, JE ;
Maquet, V ;
Notingher, I ;
Boccaccini, AR .
JOURNAL OF BIOMEDICAL MATERIALS RESEARCH PART A, 2003, 67A (04) :1401-1411
[2]
Bioresorbable and bioactive polymer/Bioglass® composites with tailored pore structure for tissue engineering applications [J].
Boccaccini, AR ;
Maquet, V .
COMPOSITES SCIENCE AND TECHNOLOGY, 2003, 63 (16) :2417-2429
[3]
Nano-fibrous poly(L-lactic acid) scaffolds with interconnected spherical macropores [J].
Chen, VJ ;
Ma, PX .
BIOMATERIALS, 2004, 25 (11) :2065-2073
[4]
Du C, 1999, J BIOMED MATER RES, V44, P407, DOI 10.1002/(SICI)1097-4636(19990315)44:4<407::AID-JBM6>3.0.CO
[5]
2-T
[6]
Du C, 1998, J BIOMED MATER RES, V42, P540, DOI 10.1002/(SICI)1097-4636(19981215)42:4<540::AID-JBM9>3.3.CO
[7]
2-U
[8]
Increased viable osteoblast density in the presence of nanophase compared to conventional alumina and titania particles [J].
Gutwein, LG ;
Webster, TJ .
BIOMATERIALS, 2004, 25 (18) :4175-4183
[9]
Osteoblast and chrondrocyte proliferation in the presence of alumina and titania nanoparticles [J].
Gutwein, LG ;
Webster, TJ .
JOURNAL OF NANOPARTICLE RESEARCH, 2002, 4 (03) :231-238
[10]
Scaffolds in tissue engineering bone and cartilage [J].
Hutmacher, DW .
BIOMATERIALS, 2000, 21 (24) :2529-2543