Chitosan-calcium phosphate composite scaffolds for control of post-operative osteomyelitis: Fabrication, characterization, and in vitro-in vivo evaluation
Radwan, Noha H; Nasr, Maha; Abdeltawab, Nourtan F; Awad, Gehanne A S; Aziz Ishak, Rania;
Abstract
Osteomyelitis is a progressive inflammatory disease requiring prolonged systemic treatment with high antibiotic doses, and is very challenging to be treated. The use of locally applied antibiotics loaded on a biodegradable carrier at surgery sites is hypothesized to prevent post-operative osteomyelitis, while providing site-specific drug release. In this work, chitosan-based calcium phosphate composites were prepared and loaded with moxifloxacin hydrochloride. The in-situ formation of calcium phosphates within the composite was experimentally confirmed by Fourier transform infra-red spectroscopy, X-ray powder diffraction, and scanning electron microscopy. Results showed that the composites provided complete drug release over three days, and the selected composite formulation induced differentiation and proliferation of osteoblasts, while reducing bacterial count, inflammation and intra-medullary fibrosis in bone tissue specimens of osteomyelitis-induced animal model. Hence, we can conclude that the in situ prepared antibiotic-loaded calcium phosphate chitosan composite is promising in preventing post-operative osteomyelitis, and is worthy of clinical experimentation.
Other data
Title | Chitosan-calcium phosphate composite scaffolds for control of post-operative osteomyelitis: Fabrication, characterization, and in vitro-in vivo evaluation | Authors | Radwan, Noha H; Nasr, Maha ; Abdeltawab, Nourtan F; Awad, Gehanne A S; Aziz Ishak, Rania | Keywords | Calcium phosphate;Chitosan;Composite;Moxifloxacin hydrochloride;Osteomyelitis;Scaffold | Issue Date | 15-Sep-2020 | Publisher | ELSEVIER SCI LTD | Journal | Carbohydrate Polymers | Volume | 244 | ISSN | 01448617 | DOI | 10.1016/j.carbpol.2020.116482 | PubMed ID | 32536391 | Scopus ID | 2-s2.0-85085733815 | Web of science ID | WOS:000541115700016 |
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