Abstract
Effective regeneration of bone defects caused by trauma or chronic diseases is a significant clinical challenge. Bone deficiency is overcome using treatments that rely on bone regeneration and augmentation. While various treatments have been investigated with encouraging results, complete and predictable bone reconstruction is often difficult [1]. Synthetic bone grafts have advantages such as consistent quality, safety, and good tissue tolerance. They usually function as inert or osteoconductive implants. Encouraging results from synthetic grafts have been reported. For instance, hollow hydroxyapatite (HA) microspheres showed the ability to facilitate bone repair in rats with non-healing calvarial defects [2,3]. However, new bone formation with the closed HA microspheres was limited. Our goal is to investigate whether open HA microsphere mediated bone repair and regeneration in an osseous model is more effective than repair mediated by closed HA microspheres. The microgeometry-, size-, and time-dependent effects of bone repair by closed and open microspheres are also compared.
Recommended Citation
Y. Shen et al., "Geometric Effects of Open Hollow Hydroxyapatite Microspheres Influence Bone Repair and Regeneration in Sprague Dawley Rats," Transactions of the Annual Meeting of the Society for Biomaterials and the Annual International Biomaterials Symposium, vol. 40, pp. 83 - 83, Society for Biomaterials, Apr 2019.
Meeting Name
42nd Society for Biomaterials Annual Meeting and Exposition 2019: The Pinnacle of Biomaterials Innovation and Excellence (2019: Apr. 3-6, Seattle, WA)
Department(s)
Materials Science and Engineering
Second Department
Biological Sciences
Keywords and Phrases
Defects; Hydroxyapatite; Microspheres; Rats; Repair, Bone reconstruction; Consistent quality; Geometric effects; Hydroxyapatite microspheres; Regeneration of bone defects; Sprague-Dawley rats; Synthetic bone grafts; Time-dependent effects, Bone
International Standard Book Number (ISBN)
978-151088390-1
International Standard Serial Number (ISSN)
1526-7547
Document Type
Article - Conference proceedings
Document Version
Final Version
File Type
text
Language(s)
English
Rights
© 2019 Omnipress, All rights reserved.
Publication Date
01 Apr 2019