2021
DOI: 10.1016/j.msec.2021.112017
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Electrically-responsive antimicrobial coatings based on a tetracycline-loaded poly(3,4-ethylenedioxythiophene) matrix

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Cited by 17 publications
(12 citation statements)
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“…Conducting polymers can also be employed as antibiotic carriers that enable electrically-triggered controlled drug release and electrically-driven antibacterial activity. In a recent study [ 137 ], a PEDOT matrix was used to immobilize a powerful first-line antibiotic (tetracycline; Tc). Although a portion of the immobilized Tc was released spontaneously, the electrical trigger (a chronoamperometric potential jump from –0.6 V to –0.5 V, applied for 2 s and 600 s, respectively) made it possible to control the overall rate of drug release.…”
Section: Control Strategies For the Formation Of Clinically Important...mentioning
confidence: 99%
“…Conducting polymers can also be employed as antibiotic carriers that enable electrically-triggered controlled drug release and electrically-driven antibacterial activity. In a recent study [ 137 ], a PEDOT matrix was used to immobilize a powerful first-line antibiotic (tetracycline; Tc). Although a portion of the immobilized Tc was released spontaneously, the electrical trigger (a chronoamperometric potential jump from –0.6 V to –0.5 V, applied for 2 s and 600 s, respectively) made it possible to control the overall rate of drug release.…”
Section: Control Strategies For the Formation Of Clinically Important...mentioning
confidence: 99%
“…In our research, we used SEM imaging to visualise the morphology of two types of biological samples representing prokaryotic and eukaryotic cells: a model Gram-negative bacterial strain Escherichia coli (DSM 30083, U5/41), and a cultured cell model of central nervous system neurons, namely rat neuroblastoma cell line B-35 (ATCC ® CRL-2754™). The details of culturing both types of cells can be found in our previous reports [ 43 , 44 , 45 ]. According to the optimised sample preparation protocol [ 43 , 44 , 45 ], cells were fixed using 3% glutaraldehyde for 24 h, then washed three times with sterile distilled water.…”
Section: Sample Preparationmentioning
confidence: 99%
“…The details of culturing both types of cells can be found in our previous reports [ 43 , 44 , 45 ]. According to the optimised sample preparation protocol [ 43 , 44 , 45 ], cells were fixed using 3% glutaraldehyde for 24 h, then washed three times with sterile distilled water. Subsequently, samples were dehydrated by immersing them for 10 min in the solutions of ethanol with increasing concentrations (30%, 50%, 70%, 80%, 90%, 95%, 99.8%), then dried for 24 h at 50 °C.…”
Section: Sample Preparationmentioning
confidence: 99%
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