Vancomycin-loaded bone substitute as a ready-to-use drug delivery system to treat osteomyelitis

• Type: Article in International Scientific Journal
• Date: 2023

Authors

Padrao, T (Author) Other; Dias, J (Author) Other; Carvalho, A (Author) Other; Pinto, MT (Author) Other; Fernando Mendes Monteiro (Author) FEUP; Sousa, SR (Author) Other

Journal

Title: Ceramics International

Vol. 49

ISSN: 0272-8842

Publisher: Elsevier

Indexing

ISI Web of Knowledge - 0 Citations

Other information

Authenticus ID: P-00Y-TY2

DOI: 10.1016/j.ceramint.2023.04.239

Abstract (EN): Affecting annually millions of people worldwide, osteomyelitis is a critical bone infection caused by pathogenic organisms which poses a serious health issue. The standard treatment involves debridement of infected bone, systemic administration of antibiotics and subsequent bone reconstruction. However, the systemic route of administration can be ineffective and associated with severe side effects. This work focused on the development of lyophilized vancomycin-loaded heparinized nanohydroxyapatite/collagen granules to facilitate clinical application, addressing infection eradication and bone regeneration. A local bone substitute delivery system was developed as an attractive alternative solution not yet commercially available. The lyophilization process has proven to be effective with a controlled release of the antibiotic for a longer period, above minimum inhibitory concentration for methicillin-resistant Staphylococcus aureus (MRSA), when compared to non-lyophilized granules. This system totally inhibits the growth of planktonic and sessile MRSA. Moreover, the material promoted osteoblasts metabolic activity and proliferation, while inducing neovascularization. Overall, this work advanced towards the deployment of a reliable solution in clinical practice developing a ready-to-use drug delivery system avoiding the process of antibiotic handling and preparation before surgery.

Language: English

Type (Professor's evaluation): Scientific

No. of pages: 12