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      Amperometric magnetobiosensors using poly(dopamine)-modified Fe3O4 magnetic nanoparticles for the detection of phenolic compounds

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          Abstract

          The synthesis of poly(dopamine)-modified magnetic nanoparticles and their biosensing application to detect phenolic compounds is reported in this work.

          Abstract

          The synthesis of poly(dopamine)-modified magnetic nanoparticles (MNPs) and their application in preparing electrochemical enzyme biosensors that are useful to detect phenolic compounds is reported in this work. MNPs of about 16 nm were synthesized by a co-precipitation method and conveniently modified with poly(dopamine). Non-modified and modified MNPs were characterized using X-ray photoelectron spectroscopy (XPS), Raman and infrared spectroscopy, X-ray diffraction (XRD) and atomic force microscopy (AFM). Horseradish peroxidase (HRP) was covalently immobilized onto the surface of the poly(dopamine)-modified MNPs via Michael addition and/or Schiff base formation and used to construct a biosensor for phenolic compounds by capturing the HRP-modified-nanoparticles onto the surface of a magnetic-modified glassy carbon electrode (GCE). Cyclic voltammetry and amperometry were used to study the electrochemical and analytical properties of the biosensor using hydroquinone (HQ) as a redox probe. Among the different phenolic compounds studied, the biosensor exhibited higher sensitivity for HQ, 1.38 A M −1 cm −2, with limits of detection and quantification of 0.3 and 1.86 μM, respectively. The analytical biosensor performance for HQ and 2-aminophenol compared advantageously with those of previous phenolic biosensors reported in the literature.

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          Facile Conjugation of Biomolecules onto Surfaces via Mussel Adhesive Protein Inspired Coatings.

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            Polydopamine--a nature-inspired polymer coating for biomedical science.

            Polymer coatings are of central importance for many biomedical applications. In the past few years, poly(dopamine) (PDA) has attracted considerable interest for various types of biomedical applications. This feature article outlines the basic chemistry and material science regarding PDA and discusses its successful application from coatings for interfacing with cells, to drug delivery and biosensing. Although many questions remain open, the primary aim of this feature article is to illustrate the advent of PDA on its way to become a popular polymer for bioengineering purposes.
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              Elucidating the structure of poly(dopamine).

              Herein we propose a new structure for poly(dopamine), a synthetic eumelanin that has found broad utility as an antifouling agent. Commercially available 3-hydroxytyramine hydrochloride (dopamine HCl) was polymerized under aerobic, aqueous conditions using tris(hydroxymethyl)aminomethane (TRIS) as a basic polymerization initiator, affording a darkly colored powder product upon isolation. The polymer was analyzed using a variety of solid state spectroscopic and crystallographic techniques. Collectively, the data showed that in contrast to previously proposed models, poly(dopamine) is not a covalent polymer but instead a supramolecular aggregate of monomers (consisting primarily of 5,6-dihydroxyindoline and its dione derivative) that are held together through a combination of charge transfer, π-stacking, and hydrogen bonding interactions. © 2012 American Chemical Society
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                Author and article information

                Journal
                AMNECT
                Analytical Methods
                Anal. Methods
                Royal Society of Chemistry (RSC)
                1759-9660
                1759-9679
                2015
                2015
                : 7
                : 20
                : 8801-8808
                Article
                10.1039/C5AY01996F
                dbe2833d-4ebe-4905-af7e-480993451d60
                © 2015
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