Affiliations 

  • 1 Department of Biomedical Engineering, Faculty of Engineering, University of Malaya, 50603 Kuala Lumpur, Malaysia. Electronic address: sara.pourshahrestani@um.edu.my
  • 2 School of Engineering, Monash University, 47500 Bandar Sunway, Selangor, Malaysia
  • 3 Department of Biomedical Engineering, Faculty of Engineering, University of Malaya, 50603 Kuala Lumpur, Malaysia. Electronic address: nahrizuladib@um.edu.my
  • 4 ACLabs - Laboratori di Chimica Applicata, Dipartimento di Ingegneria Chimica, dei Materiali e della Produzione Industriale, Università Federico II, P.le Tecchio 80, 80125 Napoli, Italy; CeSMA-Centro di Servizi Metrologici e Tecnologici Avanzati, Università Federico II, Corso N. Protopisani, 80146 Napoli, Italy
  • 5 Department of Medical Microbiology, Faculty of Medicine, University of Malaya, 50603 Kuala Lumpur, Malaysia
  • 6 Department of Biomedical Engineering, Faculty of Engineering, University of Malaya, 50603 Kuala Lumpur, Malaysia
  • 7 GLR Laboratories Pvt Ltd., Mathur, Chennai 600068, India
  • 8 Faculty of Medicine, Mahsa University College, 50603 Kuala Lumpur, Malaysia
  • 9 Tissue Engineering Group (TEG), National Orthopaedic Centre of Excellence in Research and Learning (NOCERAL), Department of Orthopaedic Surgery, Faculty of Medicine, University of Malaya, 50603 Kuala Lumpur, Malaysia
Mater Sci Eng C Mater Biol Appl, 2019 May;98:1022-1033.
PMID: 30812986 DOI: 10.1016/j.msec.2019.01.022

Abstract

A novel series of silver-doped mesoporous bioactive glass/poly(1,8-octanediol citrate) (AgMBG/POC) elastomeric biocomposite scaffolds were successfully constructed by a salt-leaching technique for the first time and the effect of inclusion of different AgMBG contents (5, 10, and 20 wt%) on physicochemical and biological properties of pure POC elastomer was evaluated. Results indicated that AgMBG particles were uniformly dispersed in the POC matrix and increasing the AgMBG concentration into POC matrix up to 20 wt% enhanced thermal behaviour, mechanical properties and water uptake ability of the composite scaffolds compared to those from POC. The 20%AgMBG/POC additionally showed higher degradation rate in Tris(hydroxymethyl)-aminomethane-HCl (Tris-HCl) compared with pure POC and lost about 26% of its initial weight after soaking for 28 days. The AgMBG phase incorporation also significantly endowed the resulting composite scaffolds with efficient antibacterial properties against Escherichia coli and Staphylococcus aureus bacteria while preserving their favorable biocompatibility with soft tissue cells (i.e., human dermal fibroblast cells). Taken together, our results suggest that the synergistic effect of both AgMBG and POC make these newly designed AgMBG/POC composite scaffold an attractive candidate for soft tissue engineering applications.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.