Evaluation of BSA Protein Release From Hollow Hydroxyapatite Microspheres into PEG Hydrogel
Editor(s)
Narayan, R.
Abstract
Implants that simultaneously function as an osteoconductive matrix and as a device for local drug or growth factor delivery could provide an attractive system for bone regeneration. In our previous work, we prepared hollow hydroxyapatite (abbreviated HA) microspheres with a high surface area and mesoporous shell wall and studied the release of a model protein, bovine serum albumin (BSA), from the microspheres into phosphate-buffered saline (PBS). The present work is an extension of our previous work to study the release of BSA from similar HA microspheres into a biocompatible hydrogel, poly(ethylene glycol) (PEG). BSA-loaded HA microspheres were placed in a PEG solution which was rapidly gelled using ultraviolet radiation. The BSA release rate into the PEG hydrogel, measured using a spectrophotometric method, was slower than into PBS, and it was dependent on the initial BSA loading and on the microstructure of the microsphere shell wall. A total of 35-40% of the BSA initially loaded into the microspheres was released into PEG over ~14 days. The results indicate that these hollow HA microspheres have promising potential as an osteoconductive device for local drug or growth factor delivery in bone regeneration and in the treatment of bone diseases.
Recommended Citation
H. Fu et al., "Evaluation of BSA Protein Release From Hollow Hydroxyapatite Microspheres into PEG Hydrogel," Materials Science and Engineering: C, Elsevier, Jan 2013.
The definitive version is available at https://doi.org/10.1016/j.msec.2013.01.048
Department(s)
Materials Science and Engineering
International Standard Serial Number (ISSN)
0928-4931
Document Type
Article - Journal
Document Version
Citation
File Type
text
Language(s)
English
Rights
© 2013 Elsevier, All rights reserved.
Publication Date
01 Jan 2013