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6 protocols using drp 220at

1

Comprehensive Characterization of Nanomaterials

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Electrochemical measurements were performed in a Metrohm Autolab potentiostat/galvanostat equipped with an FRA module and controlled by Nova 2.1.6 software. The Au-SPEs (DRP-220AT, DropSens) contained a gold working electrode (4 mm), a gold counter electrode, and a pseudo-reference electrode with silver electrical contacts. The switch box connecting these Au-SPEs to the potentiostat was obtained from DropSens. Raman studies were performed with a Thermo Fisher Scientific Company DXR Raman spectrometer using Thermo Scientific OMNIC software. Spectra were recorded in the range of 300 to 1800 using a 785-nm excitation laser through a 50 × confocal microscope objective. Laser power was set at 10 mW, with an aperture of 50 µm slit, for an acquisition time of 10 seconds. UV–Vis studies were performed using the Evolution 220 UV–Vis spectrophotometer from Thermo Fisher Scientific Company. Transmission electron microscopy (TEM) was performed using a JEOL JEM 1010 transmission electron microscope operating at an accelerating voltage of 100 kV. SEM was performed using a JEOL JSM 6301 F/Oxford INCAEnergy 350/Gatan Alto 2500 high-resolution field emission scanning electron microscope.
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2

Electrochemical Detection of Glyphosate

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Glyphosate was purchased from Sigma Aldrich Chemie GmbH, 45521, Buchs, Switzerland. Dilution series of up to 0.3 mM were prepared in local tap water (Lyngby Taarbæk municipality, Denmark) with no further treatment or purification. Water characterization can be seen in the Supplementary Material, Table S1. Tap water was also considered as the background in all measurements. Omethoate was purchased from Sigma Aldrich, 36181. Aminomethylphosphonic acid (APMA) was purchased from Sigma Aldrich, 324817. A concentration of 0.3 mM was prepared using local tap water with no further treatment or purification. All electrochemical measurements were taken with a potentiostat (PalmSens 3, PalmSens, Houten, The Netherlands). Commercial, screen-printed electrodes based on gold working and counter electrodes and a silver reference electrode were used to conduct the measurements (DRP 220AT, Dropsens, Asturias, Spain). The pH measurements were carried out using a pH meter (EUTECH Instruments pH700, Singapore). The conductivity of the water was measured using a conductivity meter (Meter Lab CDM210, Radiometer Copenhagen, Lyon, France).
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3

Electrochemical Sensing Polymer Coatings

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Disposable screen-printed gold working electrodes (WE) with silver pseudo-reference electrodes (Dropsens drp-220AT) were used for all experiments. All polymers were dissolved in DMSO to make a solution with a concentration of 20 μg/μL. The polymer solution was mixed in a 1:1 (9:1 for fluorescein) ratio with a drug solution with a concentration of 10 μg/μL in DMSO. 2 μL (1.41 μL for FL) of the resulting solution was deposited on the WE. The samples were then dried for 30 min in a 65 °C oven to ensure removal of the DMSO. 10 μL of a 0.01 % chitosan solution in 0.1 M HCL was dropcast onto the top of the sample and allowed to dry at room temperature.
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4

Electrochemical Characterization of Screen-Printed Electrodes

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Commercial screen-printed electrodes (SPE, Model No: DRP 220 AT, Φ = 4 mm), including a Au working electrode (WE) with a surface area of 12.56 mm2, were purchased from the Metrohm DropSens Co. (Oviedo, Spain). This electrode includes a Au counter electrode (CE) and a silver pseudo-reference electrode (RE). Chronoamperometry (CA) and cyclic voltammetry (CV) measurements were conducted with a multi-channel potentiostat obtained from CH instruments (Texas, TX, USA, Model No: CH 1030C) and Wismar Co. Ltd. (Daejeon, Korea, Model No: WIZECM-1200Premium). Electrochemical impedance spectroscopy (EIS) was carried out with a pocketSTAT from Ivium Technologies B.V. (AJ Eindhoven, The Netherlands). All electrochemical (EC) measurements were conducted at room temperature in a Faraday cage.
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5

Electrochemical Analysis Using Commercial SPE

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Commercial SPE (Model no: DRP 220 AT, Φ = 4 mm) was purchased from Metrohm DropSens (Asturias, Spain). CA, and CV, EIS were performed with a potentiostat obtained from CH Instruments (Texas, USA; Model no: CH 660C). All electrochemical measurements were performed at room temperature in a Faraday cage to ensure electromagnetic shielding.
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6

Electrochemical Biosensor for lncRNA Detection

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Unless otherwise stated, chemicals and reagents were used without further purification and were of analytical grade. Screen-printed gold electrodes (SPE-Au) with a three-electrode system (DRP-220AT) were purchased from Metrohm Dropsens (Spain). In the three-electrode system, working (4 mm diameter), reference and counter electrodes consisted of gold, silver/silver chloride, and platinum, respectively. UltraPureTM DNase/RNase-free distilled water was purchased from Invitrogen, Australia. Synthetic lncRNA and capture probes (Table 1) were purchased from Integrated DNA Technologies (Coralville, IA, USA). All other reagents were purchased from Sigma Aldrich (Sydney, NSW, Australia). All electrochemical measurements were performed using a 650E series electrochemical workstation potentiostat purchased from CH Instruments, Austin, TX, USA. Plasma samples (two benign and four ovarian carcinomas) were obtained from UQCCR according to the declaration of Helsinki, with approval from the Ethics Committee of the University of Queensland (approval number 2016000300) and the Ochsner Medical centre (New Orleans, LA, USA). MeT-5A, SKOV3, and OVCAR3 cell lines were cultured in the laboratory.
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