Bioactive Glass: Methods for Assessing Angiogenesis and Osteogenesis

Biomaterials are playing an increased role in the regeneration of damaged or absent bone tissue in the context of trauma, non-union, infection or congenital abnormality. Restoration of not only the physical scaffold that bone provides, but also of its homeostatic functions as a calcium store and hem...

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Published inFrontiers in cell and developmental biology Vol. 9; p. 643781
Main Authors Crush, Jos, Hussain, Ali, Seah, K. T. M., Khan, Wasim S.
Format Journal Article
LanguageEnglish
Published Frontiers Media S.A 14.06.2021
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Summary:Biomaterials are playing an increased role in the regeneration of damaged or absent bone tissue in the context of trauma, non-union, infection or congenital abnormality. Restoration of not only the physical scaffold that bone provides, but also of its homeostatic functions as a calcium store and hematopoietic organ are the gold standards of any regenerative procedure. Bioactive glasses are of interest as they can bond with the host bone and induce further both bone and blood vessel growth. The composition of the bioactive glasses can be manipulated to maximize both osteogenesis and angiogenesis, producing a 3D scaffolds that induce bone growth whilst also providing a structure that resists physiological stresses. As the primary endpoints of studies looking at bioactive glasses are very often the ability to form substantial and healthy tissues, this review will focus on the methods used to study and quantify osteogenesis and angiogenesis in bioactive glass experiments. These methods are manifold, and their accuracy is of great importance in identifying plausible future bioactive glasses for clinical use.
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Reviewed by: Francesco Baino, Politecnico di Torino, Italy; Hae-Won Kim, Institute of Tissue Regeneration Engineering (ITREN), South Korea
This article was submitted to Cell Growth and Division, a section of the journal Frontiers in Cell and Developmental Biology
Edited by: Stevo J. Najman, University of Niš, Serbia
ISSN:2296-634X
2296-634X
DOI:10.3389/fcell.2021.643781