Dual local drug delivery of vancomycin and farnesol for mitigation of MRSA infection in vivo – a pilot study

Surgical site infections after orthopaedic surgery using fracture fixation devices or endosseous implants create major surgical challenges with severe adverse effects, such as osteomyelitis. These infections are frequently caused by Staphylococcus aureus, often with high resistance to antibiotics, s...

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Main Authors: UC Woelfle, T Briggs, S Bhattacharyya, H Qu, N Sheth, C Knabe, P Ducheyne
Format: Article
Language:English
Published: AO Research Institute Davos 2020-07-01
Series:European Cells & Materials
Subjects:
Online Access:https://www.ecmjournal.org/papers/vol040/pdf/v040a03.pdf
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spelling doaj-8a94561c14b64b58b330dce0f01d25dd2020-11-25T03:11:11Zeng AO Research Institute DavosEuropean Cells & Materials1473-22622020-07-0140385710.22203/eCM.v040a03Dual local drug delivery of vancomycin and farnesol for mitigation of MRSA infection in vivo – a pilot studyUC WoelfleT BriggsS BhattacharyyaH QuN ShethC KnabeP DucheyneSurgical site infections after orthopaedic surgery using fracture fixation devices or endosseous implants create major surgical challenges with severe adverse effects, such as osteomyelitis. These infections are frequently caused by Staphylococcus aureus, often with high resistance to antibiotics, such as methicillin-resistant Staphylococcus aureus (MRSA). Due to the formation of impenetrable biofilms on implant surfaces, systemic antibiotic treatment has become exceedingly difficult. New solutions are pursued by combining several drugs using a controlled delivery system from specifically engineered implant surfaces. A sol-gel coating on titanium implants was previously developed with 20 wt % vancomycin and 30 wt % farnesol, with suppression of MRSA in vitro. The present study investigated the efficacy of sol-gel film coatings for controlled dual local delivery over 4 weeks utilising a rat infection model. The findings confirmed the viability of this new concept in vivo based on the differences observed between coatings containing vancomycin alone (SGV) and the dual-drug-containing coating with vancomycin and farnesol (SGVF). While both the SGVF and SGV coatings facilitated excellent preservation of the osseous microarchitecture, SGVF coating displayed a slightly higher potency for suppressing MRSA infiltration than SGV, in combination with a lower reactive bone remodelling activity, most likely by disturbing biofilm formation. The next step for advancing the concept of dual-drug delivery from sol-gel coatings to the clinic and confirming the promising effect of the SGVF coatings on reactive bone remodelling and suppressing MRSA infiltration is a study in a larger animal species with longer time points.https://www.ecmjournal.org/papers/vol040/pdf/v040a03.pdfantimicrobial coatingcontrolled local drug deliverysilica sol-gelvancomycinfarnesolmethicillin-resistant staphylococcus aureusin vivoosteomyelitisµct
collection DOAJ
language English
format Article
sources DOAJ
author UC Woelfle
T Briggs
S Bhattacharyya
H Qu
N Sheth
C Knabe
P Ducheyne
spellingShingle UC Woelfle
T Briggs
S Bhattacharyya
H Qu
N Sheth
C Knabe
P Ducheyne
Dual local drug delivery of vancomycin and farnesol for mitigation of MRSA infection in vivo – a pilot study
European Cells & Materials
antimicrobial coating
controlled local drug delivery
silica sol-gel
vancomycin
farnesol
methicillin-resistant staphylococcus aureus
in vivo
osteomyelitis
µct
author_facet UC Woelfle
T Briggs
S Bhattacharyya
H Qu
N Sheth
C Knabe
P Ducheyne
author_sort UC Woelfle
title Dual local drug delivery of vancomycin and farnesol for mitigation of MRSA infection in vivo – a pilot study
title_short Dual local drug delivery of vancomycin and farnesol for mitigation of MRSA infection in vivo – a pilot study
title_full Dual local drug delivery of vancomycin and farnesol for mitigation of MRSA infection in vivo – a pilot study
title_fullStr Dual local drug delivery of vancomycin and farnesol for mitigation of MRSA infection in vivo – a pilot study
title_full_unstemmed Dual local drug delivery of vancomycin and farnesol for mitigation of MRSA infection in vivo – a pilot study
title_sort dual local drug delivery of vancomycin and farnesol for mitigation of mrsa infection in vivo – a pilot study
publisher AO Research Institute Davos
series European Cells & Materials
issn 1473-2262
publishDate 2020-07-01
description Surgical site infections after orthopaedic surgery using fracture fixation devices or endosseous implants create major surgical challenges with severe adverse effects, such as osteomyelitis. These infections are frequently caused by Staphylococcus aureus, often with high resistance to antibiotics, such as methicillin-resistant Staphylococcus aureus (MRSA). Due to the formation of impenetrable biofilms on implant surfaces, systemic antibiotic treatment has become exceedingly difficult. New solutions are pursued by combining several drugs using a controlled delivery system from specifically engineered implant surfaces. A sol-gel coating on titanium implants was previously developed with 20 wt % vancomycin and 30 wt % farnesol, with suppression of MRSA in vitro. The present study investigated the efficacy of sol-gel film coatings for controlled dual local delivery over 4 weeks utilising a rat infection model. The findings confirmed the viability of this new concept in vivo based on the differences observed between coatings containing vancomycin alone (SGV) and the dual-drug-containing coating with vancomycin and farnesol (SGVF). While both the SGVF and SGV coatings facilitated excellent preservation of the osseous microarchitecture, SGVF coating displayed a slightly higher potency for suppressing MRSA infiltration than SGV, in combination with a lower reactive bone remodelling activity, most likely by disturbing biofilm formation. The next step for advancing the concept of dual-drug delivery from sol-gel coatings to the clinic and confirming the promising effect of the SGVF coatings on reactive bone remodelling and suppressing MRSA infiltration is a study in a larger animal species with longer time points.
topic antimicrobial coating
controlled local drug delivery
silica sol-gel
vancomycin
farnesol
methicillin-resistant staphylococcus aureus
in vivo
osteomyelitis
µct
url https://www.ecmjournal.org/papers/vol040/pdf/v040a03.pdf
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