4.7 Article

Highly Conductive Melanin-like Polymer Composites for Nonenzymatic Glucose Biosensors with a Wide Detection Range

期刊

ACS APPLIED POLYMER MATERIALS
卷 4, 期 4, 页码 2527-2535

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsapm.1c01818

关键词

melanin-like polymers; conductive polydopamine; electrochemical deposition; nonenzymatic glucose sensor; bioelectronics

资金

  1. National Research Foundation of Korea [NRF-2021R1A4A1022920, NRF-2020R1F1A1075944, NRF-2018K1A3A1A32055149]
  2. National Research Foundation of Korea [2018K1A3A1A32055149] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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This study successfully synthesized highly electrically conductive melanin-like polymers (eMLPs) and demonstrated their potential application in glucose detection. The electrochemical performances of eMLP were significantly improved, and the morphology could be modulated without compromising the properties.
Melanin is a natural biopolymer with a conjugated backbone that supposedly provides conductive pathways. However, few studies have synthesized electrically conductive melanin-like polymers (eMLPs) so far. In this study, highly electrically conductive melanin-like polymers (eMLPs) were electrochemically synthesized with tunable morphologies. After a bare gold electrode was coated with eMLP, the electrochemical performances were dramatically improved by a 2-order of magnitude decrease in impedance and up to a 60-fold increase in charge storage capacity. The morphology of the eMLP could be modulated by the ratios of carboxylic acid-bearing poly(L-3,4-dihydroxyphenylalanine) nanoparticles (PLDA NPs) to dopamine without compromising the electrochemical properties. Unlike conventionally insulating polydopamine, eMLP was demonstrated in glucose detection to be a nonenzymatic biosensor with high sensitivity (752.5 mu A mM(-1) cm(-2)), a low limit of detection (23 mu M), a wide linear range up to 70 mM, and physiological selectivity. This eMLP composite with superior electrochemical performances can be utilized in a wide range of bioelectronics applications from in situ biosensors to implantable bionic interfaces.

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