eCM (Eur Cell Mater / e Cells & Materials) eCM Open Access Scientific Journal
 ISSN:1473-2262         NLM:100973416 (link)         DOI:10.22203/eCM

2014   Volume No 27 – pages 332-349

Title: A biodegradable antibiotic-impregnated scaffold to prevent osteomyelitis in a contaminated in vivo bone defect model

Author: JS McLaren, LJ White, HC Cox, W Ashraf, CV Rahman, GW Blunn, AE Goodship, RA Quirk, KM Shakesheff, R Bayston, BE Scammell

Address: University of Nottingham, Academic Orthopaedics, Trauma and Sports Medicine, Queen’s Medical Centre, Nottingham, NG7 2UH, UK

E-mail: b.scammell at nottingham.ac.uk

Key Words: PLGA, biodegradable scaffold, infection, in vivo, bone ingrowth.

Publication date: June 8th 2014

Abstract: Open fractures are at risk of serious infection and, if infected, require several surgical interventions and courses of systemic antibiotics. We investigated a new injectable formulation that simultaneously hardens in vivo to form a porous scaffold for bone repair and delivers antibiotics at high concentrations to the local site of infection. Duration of antimicrobial activity against Staphylococcus aureus was determined using the serial plate transfer test. Ultimate compressive strength and porosity of the material was measured with and without antibiotics. The material was evaluated in vivo in an ovine medial femoral condyle defect model contaminated with S. aureus. Sheep were sacrificed at either 2 or 13 weeks and the defect and surrounding bone assessed using micro-computed tomography and histology. Antimicrobial activity in vitro persisted for 19-21 days. Sheep with antibiotic-free material and bacteria became infected, while those with antibiotic-containing material and bacteria did not. Similarly, new bone growth was seen in uninoculated animals with plain polymer, and in those with antibiotic polymer with bacteria, but not in sheep with plain polymer and bacteria. The antibiotic-impregnated scaffolds were effective in preventing S. aureus infections whilst supporting bone growth and repair. If translated into clinical practice, this approach might reduce the need for systemic antibiotics.

 

Article download: Pages 332-349 (PDF file)
DOI: 10.22203/eCM.v027a24