Mineralization of osteoblasts with electrospun collagen/hydroxyapatite nanofibers

被引:161
作者
Venugopal, J. [1 ]
Low, Sharon [2 ]
Choon, Aw Tar [2 ]
Kumar, T. S. Sampath [3 ]
Ramakrishna, S. [1 ]
机构
[1] Natl Univ Singapore, Div Bioengn, Singapore 117576, Singapore
[2] StemLife Sdn BhD, Kuala Lumpur 50450, Malaysia
[3] Indian Inst Technol, Dept Met & Mat Engn, Madras 600036, Tamil Nadu, India
关键词
D O I
10.1007/s10856-007-3289-x
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Regeneration of fractured or diseased bones is the challenge faced by current technologies in tissue engineering. The major solid components of human bone consist of collagen and hydroxyapatite. Collagen (Col) and hydroxyapatite (HA) have potential in mimicking natural extracellular matrix and replacing diseased skeletal bones. More attention has been focused on HA because of its crystallographic structure similar to inorganic compound found in natural bone and extensively investigated due to its excellent biocompatibility, bioactivity and osteoconductivity properties. In the present study, electrospun nanofibrous scaffolds are fabricated with collagen (80 mg/ml) and Col/HA (1:1). The diameter of the collagen nanofibers is around 265 +/- 0.64 nm and Col/HA nanofibers are 293 +/- 1.45 nm. The crystalline HA (29 +/- 7.5 nm) loaded into the collagen nanofibers are embedded within nanofibrous matrix of the scaffolds. Osteoblasts cultured on both scaffolds and show insignificant level of proliferation but mineralization was significantly (p < 0.001) increased to 56% in Col/HA nanofibrous scaffolds compared to collagen. Energy dispersive X-ray analysis (EDX) spectroscopy results proved the presence of higher level of calcium and phosphorous in Col/HA nanocomposites than collagen nanofibrous scaffolds grown osteoblasts. The results of the present study suggested that the designed electrospun nanofibrous scaffold (Col/HA) have potential biomaterial for bone tissue engineering.
引用
收藏
页码:2039 / 2046
页数:8
相关论文
共 43 条
[1]   A biodegradable composite scaffold for cell transplantation [J].
Ameer, GA ;
Mahmood, TA ;
Langer, R .
JOURNAL OF ORTHOPAEDIC RESEARCH, 2002, 20 (01) :16-19
[2]   Matrix proteins and mineralization: An overview [J].
Boskey, AL .
CONNECTIVE TISSUE RESEARCH, 1996, 35 (1-4) :357-363
[3]   Bacteriostatic properties of biomatrices against common orthopaedic pathogens [J].
Carlson, GA ;
Dragoo, JL ;
Samimi, B ;
Bruckner, DA ;
Bernard, GW ;
Hedrick, M ;
Benhaim, P .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2004, 321 (02) :472-478
[4]   INVESTIGATION INTO THE FORMATION AND MECHANICAL-PROPERTIES OF A BIOACTIVE MATERIAL BASED ON COLLAGEN AND CALCIUM-PHOSPHATE [J].
CLARKE, KI ;
GRAVES, SE ;
WONG, ATC ;
TRIFFITT, JT ;
FRANCIS, MJO ;
CZERNUSZKA, JT .
JOURNAL OF MATERIALS SCIENCE-MATERIALS IN MEDICINE, 1993, 4 (02) :107-110
[5]  
De Bruijn J. D., 1998, BIOMATERIALS SURG, P77
[6]   Immunolocalization and quantification of noncollagenous bone matrix proteins in methylmethacrylate-embedded adult human bone in combination with histomorphometry [J].
Derkx, P ;
Nigg, AL ;
Bosman, FT ;
Birkenhäger-Frenkel, DH ;
Houtsmuller, AB ;
Pols, HAP ;
van Leeuwen, JPTM .
BONE, 1998, 22 (04) :367-373
[7]   NEOCARTILAGE FORMATION INVITRO AND INVIVO USING CELLS CULTURED ON SYNTHETIC BIODEGRADABLE POLYMERS [J].
FREED, LE ;
MARQUIS, JC ;
NOHRIA, A ;
EMMANUAL, J ;
MIKOS, AG ;
LANGER, R .
JOURNAL OF BIOMEDICAL MATERIALS RESEARCH, 1993, 27 (01) :11-23
[8]   Differentiation of mesenchymal stem cells into osteoblasts on honeycomb collagen scaffolds [J].
George, Joseph ;
Kuboki, Yoshinori ;
Miyata, Teruo .
BIOTECHNOLOGY AND BIOENGINEERING, 2006, 95 (03) :404-411
[9]   FATE OF MINERALIZED AND DEMINERALIZED OSSEOUS IMPLANTS IN CRANIAL DEFECTS [J].
GLOWACKI, J ;
ALTOBELLI, D ;
MULLIKEN, JB .
CALCIFIED TISSUE INTERNATIONAL, 1981, 33 (01) :71-76
[10]  
Grande DA, 1997, J BIOMED MATER RES, V34, P211, DOI 10.1002/(SICI)1097-4636(199702)34:2<211::AID-JBM10>3.0.CO