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1.
Bioelectromagnetics ; 32(5): 367-77, 2011 Jul.
Article in English | MEDLINE | ID: mdl-21437921

ABSTRACT

Systemic treatment of biomaterial-associated bacterial infections with high doses of antibiotics is an established therapeutic concept. The purpose of this in vitro study was to determine the influence of magnetic, electromagnetic, and electric fields on gentamicin-based, antibiotic therapy. It has been previously reported that these fields are successful in the treatment of bone healing and reducing osteitis in infected tibia-pseudarthroses. Four separate experimental setups were used to expose bacterial cultures of Staphylococcus aureus both in Mueller-Hinton broth (MHB) and on Mueller-Hinton agar (MHA), in the presence of gentamicin, to (1) a low-frequency magnetic field (MF) 20 Hz, 5 mT; (2) a low-frequency MF combined with an additional alternating electric field (MF + EF) 20 Hz, 5 mT, 470 mV/cm; (3) a sinusoidal alternating electric field (EF AC) 20 Hz, 470 mV/cm; and (4) a direct current electric field (EF DC) 588 mV/cm. No significant difference between samples and controls was detected on MHA. However, in MHB each of the four fields applied showed a significant growth reduction of planktonically grown Staphylococcus aureus in the presence of gentamicin between 32% and 91% within 24 h of the experiment. The best results were obtained by a direct current EF, decreasing colony-forming units (CFU)/ml more than 91%. The application of electromagnetic fields in the area of implant and bone infections could offer new perspectives in antibiotic treatment and antimicrobial chemotherapy.


Subject(s)
Electricity , Electromagnetic Fields , Gentamicins/pharmacology , Gentamicins/radiation effects , Staphylococcus aureus/drug effects , Staphylococcus aureus/radiation effects , Anti-Bacterial Agents/pharmacology , Anti-Bacterial Agents/radiation effects , Bone Diseases, Infectious/microbiology , Culture Media , Humans , Staphylococcal Infections/microbiology , Staphylococcal Infections/prevention & control , Staphylococcus aureus/growth & development
2.
J Biomater Sci Polym Ed ; 20(10): 1439-49, 2009.
Article in English | MEDLINE | ID: mdl-19622281

ABSTRACT

Wound infection is a complication feared in surgery. The aim of this study was to develop new anti-infective coatings of surgical sutures and to compare the anti-microbial effectiveness and biocompatibility to the well-established Vicryl Plus. Synthetic absorbable PGA surgical sutures were coated with three different chlorhexidine concentrations and two different octenidine concentrations in combination with palmitic acid and lauric acid. Drug-release kinetics lasting 96 h were studied in phosphate-buffered saline at 37 degrees C. Anti-infective characteristics were determined by measuring the change in optical density of Staphylococcus aureus suspensions charged with coated sutures over time. Microorganisms adsorbed at the surface of coated sutures were assessed on blood agar plates and coated sutures eluted for 24 h were placed on bacterial lawns cultured on Mueller-Hinton plates to prove retained anti-microbial potency. A cell proliferation assay was performed to assess the degree of cytotoxicity. Anti-infective characteristics and biocompatibility were compared to Vicryl Plus. A coating technology for slow-release drug-delivery systems on surgical sutures could be developed. All coatings showed a continuous drug release within 96 h. Individual chlorhexidine and octenidine coated sutures showed superior anti-infective characteristics but inferior biocompatibility in comparison to Vicryl Plus. We conclude that the developed anti-infective suture coatings consisting of lipid-based drug-delivery systems in combination with antiseptics are highly effective against bacterial colonization in vitro; however, drug doses have to be adjusted to improve biocompatibility.


Subject(s)
Anti-Infective Agents, Local/administration & dosage , Chlorhexidine/administration & dosage , Coated Materials, Biocompatible/chemistry , Fatty Acids/chemistry , Pyridines/administration & dosage , Sutures , Animals , Anti-Infective Agents, Local/chemistry , Anti-Infective Agents, Local/pharmacology , Bacterial Adhesion/drug effects , Cell Proliferation/drug effects , Cells, Cultured , Chlorhexidine/chemistry , Chlorhexidine/pharmacology , Delayed-Action Preparations/chemistry , Fibroblasts/cytology , Imines , Lauric Acids/chemistry , Mice , Palmitic Acid/chemistry , Pyridines/chemistry , Pyridines/pharmacology , Staphylococcus aureus/drug effects , Staphylococcus aureus/growth & development , Time Factors
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