2015
DOI: 10.1016/j.ijantimicag.2014.09.008
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Ag 5 IO 6 : novel antibiofilm activity of a silver compound with application to medical devices

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Cited by 14 publications
(16 citation statements)
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“… Neutralization/disaggregation of LPS Polymyxin (B and E), Gramicidin S, Sushi peptides, PMAP-23 177,180,262 7. Alteration of membrane permeabilization Lantibiotics (nisin, gallidermin), Lytic peptides (PTP-7), Sophorolipids, Polyhexamethylene biguanide, Chlorhexidine, Pentasilver hexaoxoiodate 179,186,191,192 8. Inhibition of cell division or cell survival Pyrrhocoricin, Microcin B17 194,198 9.…”
Section: Methods For Quantification and Structural Assessment Of Biofmentioning
confidence: 99%
See 1 more Smart Citation
“… Neutralization/disaggregation of LPS Polymyxin (B and E), Gramicidin S, Sushi peptides, PMAP-23 177,180,262 7. Alteration of membrane permeabilization Lantibiotics (nisin, gallidermin), Lytic peptides (PTP-7), Sophorolipids, Polyhexamethylene biguanide, Chlorhexidine, Pentasilver hexaoxoiodate 179,186,191,192 8. Inhibition of cell division or cell survival Pyrrhocoricin, Microcin B17 194,198 9.…”
Section: Methods For Quantification and Structural Assessment Of Biofmentioning
confidence: 99%
“…This compound may consider to be used as a potent antimicrobial agent for disinfecting medical devices like catheters, implants, ventilators and wound dressing. 192 …”
Section: Alteration Of Membrane Potential or Membrane Permeabilizatiomentioning
confidence: 99%
“…Recently, the prevalence of antimicrobial drug resistance to antibiotics has been increasing therefore, the use of silver as a disinfectant is inevitable. Silver is now used in consumer products such as textiles, cosmetics, and medical instruments 10 12 in the form of nanoparticles, which are prepared by the chemical reduction of silver salts 13 . Furthermore, studies have documented its potential in water disinfection 14 17 .…”
Section: Introductionmentioning
confidence: 99%
“…The plate was transferred to a sonicator and sonicated on high for 30 min to dislodge the biofilm. Colonies were counted to determine the biofilm density on the pegs (Biofilm Growth Check) [27]. Following the rinse step and after breaking off the pegs, the MBEC lid with biofilm growth was transferred to the prepared challenge plate (fluconazole: 16–2048 μg ml −1 ; caspofungin: 2–256 μg ml −1 ; and amphotericin B: 4–512 μg ml −1 , 2× concentrated) and incubated at 36 °C for 24 h. After the antifungal challenge, colonies were counted to determine the biofilm density on the pegs.…”
Section: Methodsmentioning
confidence: 99%