Biomimetic approaches in bone tissue engineering: Integrating biological and physicomechanical strategies

The development of responsive biomaterials capable of demonstrating modulated function in response to dynamic physiological and mechanical changes in vivo remains an important challenge in bone tissue engineering. To achieve long-term repair and good clinical outcomes, biologically responsive approa...

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Veröffentlicht in:Advanced drug delivery reviews 2015-04, Vol.84, p.1-29
Hauptverfasser: Fernandez-Yague, Marc A., Abbah, Sunny Akogwu, McNamara, Laoise, Zeugolis, Dimitrios I., Pandit, Abhay, Biggs, Manus J.
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Sprache:eng
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Zusammenfassung:The development of responsive biomaterials capable of demonstrating modulated function in response to dynamic physiological and mechanical changes in vivo remains an important challenge in bone tissue engineering. To achieve long-term repair and good clinical outcomes, biologically responsive approaches that focus on repair and reconstitution of tissue structure and function through drug release, receptor recognition, environmental responsiveness and tuned biodegradability are required. Traditional orthopedic materials lack biomimicry, and mismatches in tissue morphology, or chemical and mechanical properties ultimately accelerate device failure. Multiple stimuli have been proposed as principal contributors or mediators of cell activity and bone tissue formation, including physical (substrate topography, stiffness, shear stress and electrical forces) and biochemical factors (growth factors, genes or proteins). However, optimal solutions to bone regeneration remain elusive. This review will focus on biological and physicomechanical considerations currently being explored in bone tissue engineering. Different types of scaffolds (porous matrix, nano-fiber mesh, hydrogels and microspheres) are used to deliver bioactive molecules. This can be combined with a number of physicomechanical strategies to enhance treatment of various bone tissue defects and diseases. [Display omitted]
ISSN:0169-409X
1872-8294
DOI:10.1016/j.addr.2014.09.005