MESOPOROUS SULPHATE DOPED HYDROXYAPATITE NANOPARTICLES FOR CONTROLLED RELEASE OF PROTEINS


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ALSHEMARY A. Z., Muhammed Y., SALMAN N. A., Motameni A., GÜRBÜZ R.

Ceramics - Silikaty, vol.66, no.4, pp.447-452, 2022 (SCI-Expanded) identifier identifier

  • Publication Type: Article / Article
  • Volume: 66 Issue: 4
  • Publication Date: 2022
  • Doi Number: 10.13168/cs.2022.0040
  • Journal Name: Ceramics - Silikaty
  • Journal Indexes: Science Citation Index Expanded (SCI-EXPANDED), Scopus, Aerospace Database, Chemical Abstracts Core, Communication Abstracts, Compendex, Metadex, Directory of Open Access Journals, Civil Engineering Abstracts
  • Page Numbers: pp.447-452
  • Keywords: Hydroxyapatite, Sulphate, Characterizations, Adsorption and desorption, Protein, OSTEOCONDUCTIVITY
  • Middle East Technical University Affiliated: Yes

Abstract

© 2022 University of Chemistry and Technology, Faculty of Environmental Technology. All rights reserved.The purpose of this study is to synthesize and characterize the mesoporous nanostructure of Hydroxyapatite (HA), evaluate the impact of the addition of sulphate ions (SO42-) on the microstructure properties of HA, and assess the ability of the prepared materials to be used as a carrier for Bovine serum albumin (BSA) protein. This study successfully synthesized 0.07 mole of SO42- substituted HA using the reflux microwave-assisted wet precipitation method and fully characterized it using modern techniques. In particular, XRD, XPS, Raman, FESEM, and BET techniques were used to explore the micro-structure properties of materials. The results shows that the addition of SO42- ions amplified the lattice parameters and surface area of HA, and the particles shape was changed from semi-spherical to rod like shape. Adsorption and desorption of protein molecules were evaluated using BSA protein for 24 h at 37°C. BSA loading capacity and release behaviours were significantly improved with the incorporation of SO42- ions. The SO4- HA materials hold a promising future for being used as a carrier for protein molecules.