Collagen for bone tissue regeneration

被引:703
作者
Ferreira, Ana Marina [1 ]
Gentile, Piergiorgio [1 ]
Chiono, Valeria [1 ]
Ciardelli, Gianluca [1 ,2 ]
机构
[1] Politecn Torino, Dept Mech & Aerosp Engn, I-10129 Turin, Italy
[2] CNR IPCF UOS Pisa, I-56124 Pisa, Italy
关键词
Bone; Collagen; Hydrogel; Scaffold; Tissue engineering; HISTOLOGICAL-EVALUATION; TRICALCIUM PHOSPHATE; BIOACTIVE GLASS; MIMETIC PEPTIDE; CROSS-LINKING; TRIPLE-HELIX; I COLLAGEN; SCAFFOLDS; COMPOSITE; BIOMATERIALS;
D O I
10.1016/j.actbio.2012.06.014
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
In the last decades, increased knowledge about the organization, structure and properties of collagen (particularly concerning interactions between cells and collagen-based materials) has inspired scientists and engineers to design innovative collagen-based biomaterials and to develop novel tissue-engineering products. The design of resorbable collagen-based medical implants requires understanding the tissue/organ anatomy and biological function as well as the role of collagen's physicochemical properties and structure in tissue/organ regeneration. Bone is a complex tissue that plays a critical role in diverse metabolic processes mediated by calcium delivery as well as in hematopoiesis whilst maintaining skeleton strength. A wide variety of collagen-based scaffolds have been proposed for different tissue engineering applications. These scaffolds are designed to promote a biological response, such as cell interaction, and to work as artificial biomimetic extracellular matrices that guide tissue regeneration. This paper critically reviews the current understanding of the complex hierarchical structure and properties of native collagen molecules, and describes the scientific challenge of manufacturing collagen-based materials with suitable properties and shapes for specific biomedical applications, with special emphasis on bone tissue engineering. The analysis of the state of the art in the field reveals the presence of innovative techniques for scaffold and material manufacturing that are currently opening the way to the preparation of biomimetic substrates that modulate cell interaction for improved substitution, restoration, retention or enhancement of bone tissue function. (C) 2012 Acta Materialia Inc. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:3191 / 3200
页数:10
相关论文
共 141 条
[111]   Collagen Structure and Stability [J].
Shoulders, Matthew D. ;
Raines, Ronald T. .
ANNUAL REVIEW OF BIOCHEMISTRY, 2009, 78 :929-958
[112]  
Shyh Ming Kuo, 2008, 2008 2nd International Conference on Bioinformatics and Biomedical Engineering (ICBBE '08), P1417
[113]  
Simion M, 1997, INT J ORAL MAX IMPL, V12, P159
[114]   Biodegradable microspheres for protein delivery [J].
Sinha, VR ;
Trehan, A .
JOURNAL OF CONTROLLED RELEASE, 2003, 90 (03) :261-280
[115]   Collagen scaffolds derived from a marine source and their biocompatibility [J].
Song, E ;
Kim, SY ;
Chun, T ;
Byun, HJ ;
Lee, YM .
BIOMATERIALS, 2006, 27 (15) :2951-2961
[116]   Synthesis and in vivo evaluation of a novel hydroxyapatite/collagen-alginate as a bone filler and a drug delivery carrier of bone morphogenetic protein [J].
Sotome, S ;
Uemura, T ;
Kikuchi, M ;
Chen, J ;
Itoh, S ;
Tanaka, J ;
Tateishi, T ;
Shinomiya, K .
MATERIALS SCIENCE & ENGINEERING C-BIOMIMETIC AND SUPRAMOLECULAR SYSTEMS, 2004, 24 (03) :341-347
[117]   Biomaterials for bone tissue engineering [J].
Stevens, Molly M. .
MATERIALS TODAY, 2008, 11 (05) :18-25
[118]  
Stocum D.L, 2006, REGENER BIOL MED, P251
[119]  
Suchanek W, 1998, J MATER RES, V13, P24
[120]   Indirect solid free form fabrication of local and global porous, biomimetic and composite 3D polymer-ceramic scaffolds [J].
Taboas, JM ;
Maddox, RD ;
Krebsbach, PH ;
Hollister, SJ .
BIOMATERIALS, 2003, 24 (01) :181-194