2001
DOI: 10.1016/s0022-0728(00)00496-4
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A polyaminoquinone film for dopamine entrapment and delivery

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Cited by 11 publications
(6 citation statements)
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“…To increase the amount of dopamine in the brains of patients with diseases such as Parkinson's disease, dopamine could be incorporated into the conducting polymers and be achieved higher concentrations in the local brain tissues through controlled drug delivery systems. Actually, previous three studies have reported that dopamine was cationic bind into the conducting polymer film and was released from electrodes . The conducting polymers used in these studies are poly(5‐amino‐1,4‐naphthoquinone), poly( N ‐methylpyrrolylium) poly(styrene sulfonate) (PSS), or poly(methacryloy1 chloride).…”
Section: Introductionmentioning
confidence: 99%
See 1 more Smart Citation
“…To increase the amount of dopamine in the brains of patients with diseases such as Parkinson's disease, dopamine could be incorporated into the conducting polymers and be achieved higher concentrations in the local brain tissues through controlled drug delivery systems. Actually, previous three studies have reported that dopamine was cationic bind into the conducting polymer film and was released from electrodes . The conducting polymers used in these studies are poly(5‐amino‐1,4‐naphthoquinone), poly( N ‐methylpyrrolylium) poly(styrene sulfonate) (PSS), or poly(methacryloy1 chloride).…”
Section: Introductionmentioning
confidence: 99%
“…Actually, previous three studies have reported that dopamine was cationic bind into the conducting polymer film and was released from electrodes. 26,34,35 The conducting polymers used in these studies are poly(5-amino-1,4naphthoquinone), poly(N-methylpyrrolylium) poly(styrene sulfonate) (PSS), or poly(methacryloy1 chloride). Whether PEDOT, one of the conducting polymers used for drug delivery purposes, could be utilized to incorporate dopamine is not clear.…”
Section: Introductionmentioning
confidence: 99%
“…12−14 The release of DA could also be realized by the adsorption and desorption of DA from SAMs, polymers, or nanomaterials. 15,47,48,45 However, none of these works have applications in the activation of real neurons.…”
Section: ■ Results and Discussionmentioning
confidence: 99%
“…The ionic drug of interest is electrically entrapped in the polymer as the counterion and its controlled release is achieved upon electrical switching of the polymer film on an electrode. On the basis of this process, a variety of anions, including biotin [223], neurotransmitter glutamate [224,225], and ATP [226,227], and cations, including a number of different metal ions (e.g., Cu 2+ , Fe 3+ , Ca 2+ ) [228,229], chlorpromazine [230], dopamine [231,232], and glutamic acid [233] have been electrostatically entrapped into conducting polymer films and released by electrical potential stimulus in a controlled way.…”
Section: Polymer Filmsmentioning
confidence: 99%