Open AccessPlasma‐deposited membranes for controlled release of antibiotic to prevent bacterial adhesion and biofilm formation
Author(s) -
Hendricks Sara K.,
Kwok Connie,
Shen Mingchao,
Horbett Thomas A.,
Ratner Buddy D.,
Bryers James D.
Publication year - 2000
Publication title -
journal of biomedical materials research
Language(s) - English
Resource type - Journals
eISSN - 1097-4636
pISSN - 0021-9304
DOI - 10.1002/(sici)1097-4636(200005)50:2<160::aid-jbm10>3.0.co;2-m
Subject(s) - biofilm , materials science , adhesion , biomaterial , membrane , cell adhesion , polymer , biomedical engineering , chemical engineering , bacteria , composite material , chemistry , nanotechnology , biochemistry , medicine , genetics , biology , engineering
Bacterial infection on implanted medical devices is a significant clinical problem caused by the adhesion of bacteria to the biomaterial surface followed by biofilm formation and recruitment of other cells lines such as blood platelets, leading to potential thrombosis and thromboembolisms. To minimize biofilm formation and potential device‐based infections, a polyurethane (Biospan) matrix was developed to release, in a controlled manner, an antibiotic (ciprofloxacin™) locally at the implant interface. One material set consisted of the polyetherurethane (PEU) base matrix radiofrequency glow discharge plasma deposited with triethylene glycol dimethyl ether (triglyme); the other set had an additional coating of poly(butyl methyacrylate) (pBMA). Triglyme served as a nonfouling coating, whereas the pBMA served as a controlled porosity release membrane. The pBMA‐coated PEU contained and released ciprofloxacin™ in a controlled manner. The efficacy of the modified PEU polymers against Pseudomonas aeruginosa suspensions was evaluated under flow conditions in a parallel plate flow cell. Bacterial adhesion and colonization, if any, to the test polymers were examined by direct microscopic image analysis and corroborated with destructive sampling, followed by direct cell counting. The rate of initial bacterial cell adhesion to triglyme‐coated PEU was 0.77%, and to the pBMA‐coated PEU releasing ciprofloxacin™ was 6% of the observed adhesion rates for the control PEU. However, the rate of adherent cell accumulation due to cell growth and replication was approximately the same for the triglyme‐coated PEU and the PEU controls, but was zero for the pBMA‐coated PEU releasing ciprofloxacin™. © 2000 John Wiley & Sons, Inc. J Biomed Mater Res, 50, 160–170, 2000.