Method of electrochemically modifying surface of electrode using dopamine-hyaluronic acid conjugates

US10696753B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-10696753-B2
Application numberUS-201715783553-A
CountryUS
Kind codeB2
Filing dateOct 13, 2017
Priority dateOct 14, 2016
Publication dateJun 30, 2020
Grant dateJun 30, 2020

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  1. Title

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  2. Abstract

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  5. First independent claim

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Abstract

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Provided are a method of electrically modifying an electrode surface with dopamine-hyaluronic acid conjugates and technologies to suppress adsorption of harmful biomaterials and organisms by imparting anti-fouling to the electrode surface using the same and to maintain electrical properties of the electrode. More specifically, provided is a technology of coating an electrode surface via a dopamine functional group by electrochemically oxidizing dopamine-conjugated biocompatible polysaccharide polymers around the electrode. This aims to confirm the capability of suppressing organism adhesion depending on whether or not cells are adsorbed after coating the electrode surface, and to identify that electrochemical performance of the electrode is maintained or a slight increase in electrode resistance is kept, even after the electrode coating. The surface modified electrode according to the present invention can be widely used in the field of biomaterials such as bio-electrodes, bio-sensors and cell supports.

First claim

Opening claim text (preview).

What is claimed is: 1. A method of electrochemically modifying an electrode surface comprising applying a current to an electrode immersed in a solution comprising a compound represented by the following Formula 1: wherein the compound has a molecular weight of 35 kDa to 3 MDa, and m/(m+n) is 0.03 to 0.3, and wherein the surface modification method is carried out by immersing a reference electrode and a counter electrode in the solution to form a three electrode cell and conducting a potentiostatic method. 2. The method according to claim 1 , wherein the electrode is an ITO electrode or a gold electrode, the reference electrode is a silver/silver chloride reference electrode, and the counter electrode is a Pt electrode. 3. The method according to claim 2 , wherein the solution has a concentration of the compound of 1 to 10 mg/mL and a pH of 2 to 7. 4. The method according to claim 3 , wherein the current is applied at a constant potential within a range of 0.6 to 1.6 V for 100 to 600 seconds. 5. The method according to claim 1 , wherein the compound is formed by bonding between dopamine and hyaluronic acid.

Assignees

Inventors

Classifications

  • Hyaluronic acid, i.e. HA or hyaluronan; Derivatives thereof, e.g. crosslinked hyaluronic acid (hylan) or hyaluronates · CPC title

  • Electrodes {, e.g. composition, counter electrode} · CPC title

  • Process control or regulation (controlling or regulating in general G05) · CPC title

  • Measuring photoelectron spectrum, e.g. electron spectroscopy for chemical analysis [ESCA] or X-ray photoelectron spectroscopy [XPS] · CPC title

  • C25D9/02Primary

    with organic materials · CPC title

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What does patent US10696753B2 cover?
Provided are a method of electrically modifying an electrode surface with dopamine-hyaluronic acid conjugates and technologies to suppress adsorption of harmful biomaterials and organisms by imparting anti-fouling to the electrode surface using the same and to maintain electrical properties of the electrode. More specifically, provided is a technology of coating an electrode surface via a dopam…
Who is the assignee on this patent?
Gwangju Inst Science & Tech
What technology area does this patent fall under?
Primary CPC classification C08B37/0072. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Jun 30 2020 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).