IADR Abstract Archives

Preparation of Gelatin-Hydroxyapatite Microspheres as Cell Carrier

Objectives: Microspheres have many biological applications such as drug delivery, cell carrier, etc. Bone extracellular matrix included two phases of mineral and organic. Hydroxyapatite (HAp) is the main mineral component of bone. HAp directly bonds with natural bone and is an osteoconductive and bioactive material. Gelatin is a natural polymer that increases attachment and differentiation of cells. Since these materials are components of bone extracellular matrix (ECM), they were used as microcarrier for bone cell delivery in the current study.

Methods: In this study, for making gelatin and hydroxyapatite microspheres, the method of emulsion (water in oil) was used. In this experiment, the aqueous solution was dispersed by mechanical stirrer, homogenizer, and ultrasonic homogenizer. Aqueous solution including polymer and ceramic was added dropwise into oil and was stirred. After 30 min, the solution temperature was lowered to 10°C with constant stirring. Then chilled acetone was added to stirring solution to solidify microspheres. After that, glutaraldehyde was added to the solution as crass linking agent. The microspheres were washed several times to remove residual oil. Their characteristics were followed by optical microscopy, scanning electron microscopy (SEM), and Fourier transform infrared spectroscopy (FTIR).

Results: The results showed that the use of ultrasonic homogenizer fabricated smaller and more uniform particles than the use of homogenizer, but the use of mechanical stirrer did not produce any microspheres. The FTIR result showed that several times washing microspheres removed residual oil and glutaraldehyde from microspheres.

Conclusions: This study showed that dispersion of the aqueous phase by different tools effects the size of particles. Since these particles are used as cell carrier, the size and distribution of microspheres is important. The methods which make smaller and more uniform microspheres are better than those for cell culture and cell carrier.


Division: Iranian Division Meeting
Meeting: 2013 Iranian Division Meeting (Tehran, Iran)
Location: Tehran, Iran
Year: 2013
Final Presentation ID:
Abstract Category|Abstract Category(s): Scientific Program
Authors
  • Alasvand, Neda  ( Department of biomaterial,School of Biomedical Engineering, Azad University Science and Research Branch, Tehran, , Iran )
  • Nojehdehyan, Hanieh  ( Department of Dental Materials, School of Dentistry, Shahid Beheshti University of Medical Sciences, Tehran, , Iran )
  • SESSION INFORMATION
    Poster Session
    Poster 4
    12/12/2013