14 آذر 1403
محمود پاك نيت جهرمي

محمود پاک نیت جهرمی

مرتبه علمی: استادیار
نشانی: دانشکده علوم و فناوری نانو و زیستی - گروه شیمی
تحصیلات: دکترای تخصصی / شیمی تجزیه
تلفن: 09171758236
دانشکده: دانشکده علوم و فناوری نانو و زیستی

مشخصات پژوهش

عنوان
اندازه گیری ولتامتری دوپامین، اوریک اسید و آسکوربیک اسید با استفاده از یک الکترود اصلاح شده با نانو ذرات نقره
نوع پژوهش پارسا
کلیدواژه‌ها
electrochemistry, silver nanoparticles, dopamine. ascorbic acid, uric acid
پژوهشگران فاطمه نورمحمد (دانشجو) ، صدیقه هاشم نیا (استاد راهنما) ، محمود پاک نیت جهرمی (استاد مشاور)

چکیده

Dopamine (DA), uric acid (UA) and Ascorbic acid (AA) are important human body compounds that play determining role in metabolism; therefore monitoring their concentration in biological fluids is important. They are electrochemically active compounds and electrochemical techniques can be used to investigate them. The main goal of this study was to design of a new carbon paste electrode modified with silver nanoparticles to use in an electrochemical study of dopamine in the absence and presence of ascorbic acid and uric acid. After the synthesis of the nanosized silver colloids by a chemical reduction process in aqueous solution in the presence of polyvinylpyrrolidone (PVP) as a stabilizing agent, a silver nanoparticle modified carbon paste electrode was prepared. Then the modified electrode was used to study electrochemical properties of DA using cyclic and differential-pulse voltammetric techniques. The cyclic voltammetric results indicate that the modified electrode can remarkably enhance electrocatalytic activity toward the oxidation and reduction of dopamine in pH3 asetate buffer solution than carbon paste electrode. The electrochemical process was observed to be diffusion-controlled, quasi-reversible and involving two-electron oxidation. Under optimal conditions, the anodic peak current was proportional to DA concentration in the range of 5.0 to 430.0 ?M with a detection limit of 1.0 ?M using differential pulse voltammetry. The linear range of DA in the presence of UA and AA was from 5.0 to 70.0 and 15.0 to 170.0 µ M with a detection limit of 1.68 and 7.6 respectively. The electrode can also use for selective determination of DA in the presence of a mixture of AA and UA in phosphate buffer solution (pH 7.0). Results showed a linear dynamic range of DA extended from 12.5 to 300.0 µM and a detection limit of 1.1µM.