Abstract
Antimicrobial releasing biomaterial coatings have found application for instance in the fixation of orthopedic joint prostheses and central venous catheters. Most frequently, the release kinetics is such that antimicrobially-effective concentrations are only reached within the first days to weeks after implantation, leaving no local antimicrobial release available when a biomaterial-associated infection occurs later. Here we compare the ad libitum release of chlorhexidine and silver-sulfadiazine from a central venous catheter with their release from a new, on-demand release coating consisting of a temperature-sensitive copolymer of styrene and n-butyl (meth)acrylate. The copolymer can be loaded with an antimicrobial, which is released when the temperature is raised above its glass transition temperature. Ad libitum release of chlorhexidine and silver-sulfadiazine from a commercially-purchased catheter and associated antimicrobial efficacy against Staphylococcus aureus was limited to 16 days. Consecutive temperature-triggers of our on-demand coating yielded little or no antimicrobial efficacy of silver-acetate release, but antimicrobially-effective chlorhexidine concentrations were observed over a time period of 60-80 days. This attests to the clear advantage of on-demand coatings above ad libitum releasing coatings, that may have released their antimicrobial content before it is actually needed. Importantly, glass transition temperature of chlorhexidine loaded copolymers was lower (48 °C) than of silver loaded ones (61 °C), facilitating their clinical use. © 2014 Elsevier B.V.
Original language | English |
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Pages (from-to) | 61-66 |
Number of pages | 6 |
Journal | Journal of Controlled Release |
Volume | 188 |
DOIs | |
Publication status | Published - 28-Aug-2014 |
Keywords
- Biofilms
- Central venous catheters
- Chlorhexidine
- Infection
- Silver
- chlorhexidine
- styrene
- sulfadiazine silver
- antimicrobial catheter
- article
- central venous catheter
- comparative study
- concentration response
- controlled drug release
- controlled study
- drug coating
- drug release
- glass transition temperature
- heat sensitivity
- high temperature
- nonhuman
- priority journal
- Staphylococcus aureus