2014
DOI: 10.1002/adfm.201401377
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A Photoresponsive Red‐Hair‐Inspired Polydopamine‐Based Copolymer for Hybrid Photocapacitive Sensors

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Cited by 32 publications
(39 citation statements)
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“…As an example, multilayered polyelectrolyte films made from PDA particles and polyamines like poly‐(L‐lysine hydrobromide) (PLL) and pure PDA grains in suspension in the cell culture medium were found to affect melanoma cell growth in different manners (Eap et al., ). Copolymerization of dopamine with 5‐ S ‐cysteinyldopamine (CDA) is a useful means of controlling and modifying PDA structure to change electrical properties and impart photocapacitor‐like behavior (Ambrico et al., ). The analogy in the structure and properties of dopamine‐CDA copolymers with those of neuromelanin (Wakamatsu et al., ) and the photoresponsive behavior of CDA polymers akin to that of pheomelanins (Napolitano et al., ) reinforces the value of melanin biochemistry and biophysics as a source of inspiration for functional biomaterials (Della Vecchia et al., ).…”
Section: Applicationsmentioning
confidence: 99%
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“…As an example, multilayered polyelectrolyte films made from PDA particles and polyamines like poly‐(L‐lysine hydrobromide) (PLL) and pure PDA grains in suspension in the cell culture medium were found to affect melanoma cell growth in different manners (Eap et al., ). Copolymerization of dopamine with 5‐ S ‐cysteinyldopamine (CDA) is a useful means of controlling and modifying PDA structure to change electrical properties and impart photocapacitor‐like behavior (Ambrico et al., ). The analogy in the structure and properties of dopamine‐CDA copolymers with those of neuromelanin (Wakamatsu et al., ) and the photoresponsive behavior of CDA polymers akin to that of pheomelanins (Napolitano et al., ) reinforces the value of melanin biochemistry and biophysics as a source of inspiration for functional biomaterials (Della Vecchia et al., ).…”
Section: Applicationsmentioning
confidence: 99%
“…Synthetic eumelanins may feature chemical and morphological diversity which affects a number of key properties of relevance for bioelectronic applications (Ambrico et al., ), in particular electrical conduction (Meredith et al., ; Mostert et al., ,b). Several groups have published various device architectures with applications such as memory (metal–insulator–semiconductor geometries) (Ambrico et al., , ), batteries (Kim et al., ), and biomimetic interfaces (Ambrico et al., ; Wünsche et al., ). The device fabrication, and consequently the device performance, is affected by parameters such as melanin precursor and oxidizing system/conditions during eumelanin synthesis.…”
Section: Applicationsmentioning
confidence: 99%
“…However, based on the hydration dependence of those properties, more recent research shows that the melanin structure is best described as a hybrid ionic–electronic conductor in which both electrons and protons released by comproportionation are involved in electrical conduction ( Figure ) . Polydopamine exhibits the same hybrid ionic–electronic conductivity as natural eumelanins, which has already been exploited variously and provides great potential for use in bioelectronic devices that are capable of integration with living tissue …”
Section: Catecholamine Polymers: Chemistry and Structurementioning
confidence: 99%
“…For instance, dopamine modified with bromoisobutyryl bromide when applied with unmodified dopamine (1:1 molar ratio) creates a polydopamine macroinitiator coating suitable for subsequent surface initiation of radical polymerization . Dopamine has also been modified with l ‐cysteine to create 5‐S‐cysteinyldopamine, which has been polymerized on its own and with polydopamine to make synthetic pheomelanin . Another example of dopamine modification is its reaction with 1,3‐propane sultone, making a sulfonate variant that has been used to present a negatively charged coating surface to allow better dispersion of coated particles …”
Section: Catecholamine Polymers: Chemistry and Structurementioning
confidence: 99%
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