Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2016 Apr;6(2):184-94.
doi: 10.1007/s13346-015-0233-3.

Growth factor-eluting technologies for bone tissue engineering

Affiliations
Review

Growth factor-eluting technologies for bone tissue engineering

Ethan Nyberg et al. Drug Deliv Transl Res. 2016 Apr.

Abstract

Growth factors are essential orchestrators of the normal bone fracture healing response. For non-union defects, delivery of exogenous growth factors to the injured site significantly improves healing outcomes. However, current clinical methods for scaffold-based growth factor delivery are fairly rudimentary, and there is a need for greater spatial and temporal regulation to increase their in vivo efficacy. Various approaches used to provide spatiotemporal control of growth factor delivery from bone tissue engineering scaffolds include physical entrapment, chemical binding, surface modifications, biomineralization, micro- and nanoparticle encapsulation, and genetically engineered cells. Here, we provide a brief review of these technologies, describing the fundamental mechanisms used to regulate release kinetics. Examples of their use in pre-clinical studies are discussed, and their capacities to provide tunable, growth factor delivery are compared. These advanced scaffold systems have the potential to provide safer, more effective therapies for bone regeneration than the systems currently employed in the clinic.

Keywords: Biomaterials; Bone scaffold; Osteogenesis; Stem cells; Tissue engineering.

PubMed Disclaimer

Similar articles

Cited by

References

    1. Adv Funct Mater. 2014 May 28;24(20):3082-3093 - PubMed
    1. Tissue Eng Part A. 2012 Feb;18(3-4):331-41 - PubMed
    1. Tissue Eng Part A. 2013 Sep;19(17-18):2076-86 - PubMed
    1. Biomaterials. 2004 Feb;25(4):677-85 - PubMed
    1. J Biomater Sci Polym Ed. 2014;25(17):1875-90 - PubMed

Publication types

MeSH terms

Substances

LinkOut - more resources