Angiogenic Effects of Borate Glass Microfibers in a Rodent Model
The primary objective of this research was to evaluate the use of bioactive borate-based glass microfibers for angiogenesis in soft tissue repair applications. The effect of these fibers on growth of capillaries and small blood vessels was compared to that of 45S5 silica glass microfibers and sham implant controls. Compressed mats of three types of glass microfibers were implanted subcutaneously in rats and tissues surrounding the implant sites histologically evaluated 2-4 weeks post surgery. Bioactive borate glass 13-93B3 supplemented with 0.4 wt % copper promoted extensive angiogenesis as compared to silica glass microfibers and sham control tissues. The angiogenic responses suggest the copper-containing 13-93B3 microfibers may be effective for treating chronic soft tissue wounds. A second objective was to assess the possible systemic cytotoxicity of dissolved borate ions and other materials released from implanted borate glass microfibers. Cytotoxicity was assessed via histological evaluation of kidney tissue collected from animals 4 weeks after subcutaneously implanting high amounts of the borate glass microfibers. The evaluation of the kidney tissue from these animals showed no evidence of chronic histopathological changes in the kidney. The overall results indicate the borate glass microfibers are safe and effective for soft tissue applications.
Y. Lin et al., "Angiogenic Effects of Borate Glass Microfibers in a Rodent Model," Journal of Biomedical Materials Research Part A, vol. 102, no. 12, pp. 4491-4499, John Wiley & Sons Inc., Dec 2014.
The definitive version is available at https://doi.org/10.1002/jbm.a.35120
Materials Science and Engineering
Keywords and Phrases
Angiogenesis; Borate glass microfibers; Microvessels; Subcutaneous tissue; Animals; Bioactive glass; Blood vessels; Copper; Glass; Histology; Microcirculation; Repair; Silica
International Standard Serial Number (ISSN)
Article - Journal
© 2014 John Wiley & Sons Inc., All rights reserved.
01 Dec 2014