Surface Characterization and Physiochemical Evaluation of P(3HB- co -4HB)-Collagen Peptide Scaffolds with Silver Sulfadiazine as Antimicrobial Agent for Potential Infection-Resistance Biomaterial.

Autor: Vigneswari S; Faculty of Science and Marine Environment, Universiti Malaysia Terengganu, Kuala Terengganu 21030, Terengganu, Malaysia., Gurusamy TP; School of Biological Sciences, Universiti Sains Malaysia, Gelugor 11800, Penang, Malaysia., Khairul WM; Faculty of Science and Marine Environment, Universiti Malaysia Terengganu, Kuala Terengganu 21030, Terengganu, Malaysia., H P S AK; School of Industrial Technology, Universiti Sains Malaysia, Gelugor 11800, Penang, Malaysia., Ramakrishna S; Center for Nanofibers and Nanotechnology, Department of Mechanical Engineering, National University of Singapore, Singapore 117581, Singapore., Amirul AA; School of Biological Sciences, Universiti Sains Malaysia, Gelugor 11800, Penang, Malaysia.; Centre for Chemical Biology, Universiti Sains Malaysia, Bayan Lepas 11900, Penang, Malaysia.; Malaysian Institute of Pharmaceuticals and Nutraceuticals, NIBM, Gelugor 11700, Penang, Malaysia.
Jazyk: angličtina
Zdroj: Polymers [Polymers (Basel)] 2021 Jul 26; Vol. 13 (15). Date of Electronic Publication: 2021 Jul 26.
DOI: 10.3390/polym13152454
Abstrakt: Poly(3-hydroxybutyrate- co -4-hydroxybutyrate) [P(3HB- co -4HB)] is a bacterial derived biopolymer widely known for its unique physical and mechanical properties to be used in biomedical application. In this study, antimicrobial agent silver sulfadiazine (SSD) coat/collagen peptide coat-P(3HB- co -4HB) (SCCC) and SSD blend/collagen peptide coat-P(3HB- co -4HB) scaffolds (SBCC) were fabricated using a green salt leaching technique combined with freeze-drying. This was then followed by the incorporation of collagen peptides at various concentrations (2.5-12.5 wt.%) to P(3HB- co -4HB) using collagen-coating. As a result, two types of P(3HB- co -4HB) scaffolds were fabricated, including SCCC and SBCC scaffolds. The increasing concentrations of collagen peptides from 2.5 wt.% to 12.5 wt.% exhibited a decline in their porosity. The wettability and hydrophilicity increased as the concentration of collagen peptides in the scaffolds increased. In terms of the cytotoxic results, MTS assay demonstrated the L929 fibroblast scaffolds adhered well to the fabricated scaffolds. The 10 wt.% collagen peptides coated SCCC and SBCC scaffolds displayed highest cell proliferation rate. The antimicrobial analysis of the fabricated scaffolds exhibited 100% inhibition towards various pathogenic microorganisms. However, the SCCC scaffold exhibited 100% inhibition between 12 and 24 h, but the SBCC scaffolds with SSD impregnated in the scaffold had controlled release of the antimicrobial agent. Thus, this study will elucidate the surface interface-cell interactions of the SSD-P(3HB- co -4HB)-collagen peptide scaffolds and controlled release of SSD, antimicrobial agent.
Databáze: MEDLINE
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