2021
DOI: 10.3390/polym13121948
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Dopant-Dependent Electrical and Biological Functionality of PEDOT in Bioelectronics

Abstract: The aspiration to interact living cells with electronics challenges researchers to develop materials working at the interface of these two distinct environments. A successful interfacing coating should exhibit both biocompatibility and desired functionality of a bio-integrated device. Taking into account biodiversity, the tissue interface should be fine-tuned to the specific requirements of the bioelectronic systems. In this study, we pointed to electrochemical doping of conducting polymers as a strategy enabl… Show more

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Cited by 17 publications
(9 citation statements)
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References 62 publications
(79 reference statements)
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“…20,37,43,44 When the glial scar becomes too bushy and the neurons around the electrode die due to inflammation (acute and chronic), 45,46 the electrode loses its function. So far, methods for perfecting the compatibility of bioelectrodes include: (i) surface coating; 47 (ii) doping; 48 (iii) covalent grafting; 49 and (iv) layer-by-layer self-assembly technology based on electrostatic attraction. 50…”
Section: Neural Electrode–tissue Interfacesmentioning
confidence: 99%
“…20,37,43,44 When the glial scar becomes too bushy and the neurons around the electrode die due to inflammation (acute and chronic), 45,46 the electrode loses its function. So far, methods for perfecting the compatibility of bioelectrodes include: (i) surface coating; 47 (ii) doping; 48 (iii) covalent grafting; 49 and (iv) layer-by-layer self-assembly technology based on electrostatic attraction. 50…”
Section: Neural Electrode–tissue Interfacesmentioning
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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