Nanomolar simultaneous determination of Ascorbic acid, Epinephrine,Acetaminophen, L-Tryptophan and L-Tyrosine on a glassy carbon electrodecoated with γ-MnO2/PPy/RGO nanocomposite

سال انتشار: 1395
نوع سند: مقاله کنفرانسی
زبان: انگلیسی
مشاهده: 242

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شناسه ملی سند علمی:

ELECTROCHEMISTRY012_021

تاریخ نمایه سازی: 5 آذر 1397

چکیده مقاله:

Ascorbic acid (AA), Epinephrine (EPI), Acetaminophen (ACT), L-Tryptophan (Trp) and LTyrosine(Tyr) are biochemical compounds which play important roles in various biologicalprocesses. Usually, they are co-existing substances in biological matrices. Altering theconcentration of these species cause to several diseases, so their determination in human fluidssuch as blood plasma is much essential. These facts have encouraged chemists to developfaster, simpler, and more sensitive techniques such as electrochemistry to meet the variousdemands using chemically modified electrodes. This is the first report of simultaneousdetermination of these compounds. Graphene has been used for the sensitive determination ofvarious drugs molecules, due to their excellent conductivity because of π-π staking andsynergetic effects with other materials [1,2]. Polypyrrole has been considered as one of the mostpromising electrode materials to enhance the sensing sensitivity because of its low cost, easysynthesis, relatively high conductivity and good electrochemical/mechanical properties [3-5].Among various metal oxides, manganese dioxides (MnO2) have drawn great attention becauseof its high activity, non-toxicity, low cost, beneficial physicochemical property, relativelyenvironmentally benign and good electrochemical properties [6].The morphology and structure of the nanocomposite were characterized by the field emissionscaning electron microscopy (FE-SEM), Energy-dispersive X-ray spectroscopy (EDS), X-raydiffraction (XRD) and raman spectroscopy. Among the bare (GCE), RGO/GCE,PPy/RGO/GCE and γ-MnO2/PPy/RGO/GCE modified electrode namely γ-MnO2/PPy/RGO/GCE exhibited much higher electrocatalytic activities toward oxidation ofAA, EPI, ACT, Trp and Tyr. The measurements were carried out in pH 7.0 PBS, by Cyclicvoltammetry (CV) at a scan rate of 100 mV/s, Differential pulse voltammetry (DPV) at a scanrate of 50 mV/s and Amperometry. The modified electrode gave five separated oxidation peaksat 150 mV, 410 mV, 600 mV, 780 mV and 990 mV for AA, EPI, ACT, Trp and Tyrrespectively. Under optimum conditions, DPV indicated linear relationships between oxidationpeak current and AA, EPI, ACT, Trp and Tyr concentrations in the ranges of 1-360 μM, 0.5-410 μM, 0.4-470 μM, 2-190 μM and 0.2-105 μM with detection limits of 0.04 μM, 0.032 μM,0.033 μM, 0.018 μM and 0.008 μM respectively. Under optimum conditions, amperometryindicated linear relationships between oxidation peak current and AA, EPI, ACT, Trp and Tyrconcentrations in the ranges of 2-450 μM, 1-540 μM, 0.8-660 μM, 3-220 μM and 0.5-160 μMwith detection limits of 0.1 μM, 0.084 μM, 0.075 μM, 0.056 μM and 0.035 μM respectivelyThe sensor provided a good performance for the simultaneous determination of AA, EPI, ACT,Trp and Tyr by not only greatly enhanced their current responses, but also resolved theoverlapping peak potentials as well as decreased the over potentials. In addition, the sensor wassuccessfully applied for the determination of these species in human blood real samples.

نویسندگان

Kh Ghanbari

Department of Chemistry, School of Science, Alzahra University, Vanak, Tehran, Iran

S Bonyadi

Department of Chemistry, School of Science, Alzahra University, Vanak, Tehran, Iran