Loading…

Simple Melatonin Determination Using Disposable and Low-Cost Lab-Made Screen-Printed Carbon Electrode

This work describes the preparation and application of a screen-printed electrode (SPE) for direct melatonin (MT) determination in samples of saliva and urine. The low-cost SPE was obtained using a simple and feasible 2D printing methodology and a lab-made conductive ink based on graphite powder and...

Full description

Saved in:
Bibliographic Details
Published in:Journal of the Electrochemical Society 2022-03, Vol.169 (3), p.37503
Main Authors: Gevaerd, Ava, Watanabe, Emily Y., Janegitz, Bruno C., Bergamini, Márcio F., Marcolino-Junior, Luiz H.
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:This work describes the preparation and application of a screen-printed electrode (SPE) for direct melatonin (MT) determination in samples of saliva and urine. The low-cost SPE was obtained using a simple and feasible 2D printing methodology and a lab-made conductive ink based on graphite powder and colorless nail polish. The proposed electrode showed similar electrochemical performance compared to a commercial SPE towards melatonin oxidation. Based on electrooxidation of melatonin recorded at +0.62 V an electroanalytical method was developed using the lab-made SPE under square wave voltammetric conditions. Repeatability and reproducibility studies showed that the relative peak current values did not show significant differences between them. Under optimized parameters inherent to the methodology and voltammetric technique, the proposed SPE presented a linear dynamic range (LDR) between 0.25 to 75.0 μ mol L −1 (R2 = 0.99), and calculated limit of detection (LOD) and limit of quantification (LOQ) of 25.8 and 83.3 nmol L −1 , respectively, were obtained. The effect of other biologically relevant compounds such as glucose, urea, and estradiol was investigated, and non-significative signal interference was observed. The method proposed was successfully applied to MT determination in spiked samples providing good recovery values between 95.6 to 104%.
ISSN:0013-4651
1945-7111
DOI:10.1149/1945-7111/ac56a2