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dc.contributor.authorRaad, Issam
dc.contributor.authorChatzinikolaou, Ioannis
dc.contributor.authorChaiban, Gassan
dc.contributor.authorHanna, Hend
dc.contributor.authorHachem, Ray
dc.contributor.authorDvorak, Tanya
dc.contributor.authorCook, Guy S.
dc.contributor.authorCosterton, J. William
dc.date.accessioned2017-08-08T21:45:21Z
dc.date.available2017-08-08T21:45:21Z
dc.date.issued2003-10
dc.identifier.citationRaad, I., I. Chatzinikolaou, G. Chaiban, H. Hanna, R. Hachem, T. Dvorak, G. Cook and J.W. Costerton, "In vitro and ex vivo activities of minocycline and edta against microorganisms embedded in biofilm on catheter surfaces," Antimicrob. Agents Chemother., 47(11):3580-3585 (2003).en_US
dc.identifier.issn0066-4804
dc.identifier.urihttps://scholarworks.montana.edu/xmlui/handle/1/13464
dc.description.abstractMinocycline-EDTA (M-EDTA) flush solution has been shown to prevent catheter-related infection and colonization in a rabbit model and in hemodialysis patients. We undertook this study in order to determine the activities of M-EDTA against organisms embedded in fresh biofilm (in vitro) and mature biofilm (ex vivo). For the experiment with the in vitro model, a modified Robbin's device (MRD) was used whereby 25 catheter segments were flushed for 18 h with 10(6) CFU of biofilm-producing Staphylococcus epidermidis, Staphylococcus aureus, and Candida albicans per ml. Subsequently, each of the catheter segments was incubated in one of the following solutions: (i) streptokinase, (ii) heparin, (iii) broth alone, (iv) vancomycin, (v) vancomycin-heparin, (vi) EDTA, (vii) minocycline (high-dose alternating with low-dose), or (viii) M-EDTA (low-dose minocycline alternating with high-dose minocycline were used to study the additive and synergistic activities of M-EDTA). All segments were cultured quantitatively by scrape sonication. For the experiment with the ex vivo model, 54 catheter tip segments removed from patients and colonized with bacterial organisms by roll plate were longitudinally cut into two equal segments and exposed to either saline, heparin, EDTA, or M-EDTA (with high-dose minocycline). Subsequently, all segments were examined by confocal laser electron microscopy. In the in vitro MRD model, M-EDTA (with a low concentration of minocycline) was significantly more effective than any other agent in reducing colonization of S. epidermidis, S. aureus, and C. albicans (P < 0.01). M-EDTA (with a high concentration of minocycline) eradicated all staphylococcal and C. albicans organisms embedded in the biofilm. In the ex vivo model, M-EDTA (with a high concentration of minocycline) reduced bacterial colonization more frequently than EDTA or heparin (P < 0.01). We concluded that M-EDTA is highly active in eradicating microorganisms embedded in fresh and mature biofilm adhering to catheter surfaces.en_US
dc.titleIn vitro and ex vivo activities of minocycline and edta against microorganisms embedded in biofilm on catheter surfacesen_US
dc.typeArticleen_US
mus.citation.extentfirstpage3580en_US
mus.citation.extentlastpage3585en_US
mus.citation.issue11en_US
mus.citation.journaltitleAntimicrobial Agents and Chemotherapyen_US
mus.citation.volume47en_US
mus.identifier.categoryEngineering & Computer Scienceen_US
mus.identifier.doi10.1128/aac.47.11.3580-3585.2003en_US
mus.relation.collegeCollege of Engineeringen_US
mus.relation.departmentCenter for Biofilm Engineering.en_US
mus.relation.departmentChemical & Biological Engineering.en_US
mus.relation.departmentChemical Engineering.en_US
mus.relation.universityMontana State University - Bozemanen_US
mus.relation.researchgroupCenter for Biofilm Engineering.en_US
mus.data.thumbpage3en_US


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