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Herein, we report the electrochemical monitoring of attoliters of water droplets in an organic medium by the electrolysis of an extracted redox species from the continuous phase upon collisional events on an ultramicroelectrode. To obtain information about a redox-free water droplet in an organic solvent, redox species with certain concentrations need to be contained inside it. The redox species inside the droplet were delivered by a partitioning equilibrium between the organic phase and the water droplets. The mass transfer of the redox species from the surrounding organic phase to the droplet is very fast because of the radial diffusion, which resultantly establishes the equilibrium. Upon the collisional contact between the droplet and the electrode, the extracted redox species in the water droplets were selectively electrolyzed, even though the redox species in the organic continuous phase remained unreacted because of the different solvent environments. The electrolysis of the redox species in the droplets, where the concentration is determined by the equilibrium constant of the redox species in water/oil, can be used to estimate the size of single water droplets in an organic solution. [ABSTRACT FROM AUTHOR]

We report enhanced electrochemical detection of single water-in-oil emulsion droplets using the nano-impact method. To detect the emulsion droplets, the water molecules in the droplets were directly oxidized (i.e., water splitting) without additional electroactive species when the droplets collided with the ultramicroelectrode. The water molecules in the emulsion droplet cannot be directly electrolyzed in an organic solvent because the emulsifier does not require a hydrophobic electrolyte. To enhance the signal intensity, the electrochemistry of sub-microscale single droplets was investigated considering the charge neutrality and limiting reagent. Therefore, effective electrolysis of the droplets was achieved. Approximately 10% of water molecules in the droplet (55.6 M H2O) were oxidized based on calculations from the electrochemical peak analysis and DLS measurements. [ABSTRACT FROM AUTHOR]

We studied the electrochemical detection of single nanosized water emulsion droplets in organic solution using the electrochemical collision technique on an ultramicroelectrode (UME). In this experiment, the detection system for water droplets does not require any kind of redox species in organic solvent. Only water molecules in the water droplets were considered. When water droplets collided with the UME surface, anodic current spikes were observed in the chronoamperometry, resulting from the electrolysis of water molecules in the water droplets. From the collision frequency and integrated current spike, concentrations and size distributions of water droplets in organic solvent can be determined. [ABSTRACT FROM AUTHOR]

We have demonstrated electrochemical detection of reduced graphene oxide (rGO) nanoparticles on an ultramicroelectrode (UME) in aqueous solution using rGO collision events. The collision phenomena are detected by monitoring a current-time transient. To attract the rGO to the UME surface, a positive electric field was developed near the UME using a redox reaction. As model systems, ferrocenemethanol and ferrocyanide oxidation reactions were adopted. Amperometric current measurements showed a staircase current response after attachment of rGO on the UME surface. The magnitude of the staircase current is given by the stepwise increase in current, which can provide insight into the size distribution of the rGO colliding with the UME. In the presence of higher concentrations of rGO, multiple collision events happened sequentially on the UME. In this case, an increasing current trend, rather than a single staircase current, was observed. The overall current increment for a given time is a measure of the concentration of rGO in solution. By using this method, charged conductive materials in an aqueous solution can be sensitively detected and/or accumulated. [ABSTRACT FROM AUTHOR]

Blood tests (e.g., red blood cell (RBC) count) are crucial for detecting, diagnosing, and monitoring the progression of blood disorders. Here, we report the development of a new and rapid method for electrochemically detecting RBCs using single-particle collision events. The principle of this method relies on the electrochemical oxidation of an electroactive redox species (potassium ferrocyanide) hindered by an RBC attached to an electrode surface. A decrease in staircase current, caused by the collision of RBCs on the electrode, was observed. The magnitude of this current decrease could provide quantitative information on the size and concentration of RBCs, which could be converted into the mean corpuscular volume (MCV) and used for diagnosis. Anemia-related diseases caused by abnormal count of RBCs (e.g., erythrocytosis, pernicious anemia) or abnormal RBC size (e.g. megaloblastic anemia, microcytic anemia) could be detected easily and quickly using this electrochemical collision method, potentially leading to extensive applications in hematology and point-of-care blood testing devices. [ABSTRACT FROM AUTHOR]

Abstract: In this work an electrochemical protein detection based on enzymatic silver deposition has been proposed and applied to the detection of thrombin. The target protein, thrombin, was first captured by thrombin binding thiolated aptamer self-assembled monolayers (SAMs) on the gold electrode surface, and then sandwiched with another biotinylated thrombin binding aptamer for the association of alkaline phosphatase (Av-ALP). The attached Av-ALP enzymatically converts the nonelectroactive substrate p-aminophenyl phosphate (p-APP) to p-aminophenol (p-AP) which can reduce silver ions in solution leading to deposition of the metal onto the electrode surface. Finally, linear sweep voltammetry (LSV) is used to detect the amount of deposited silver. The peak current during the anodic scan was found to reflect the amount of the target protein captured into the sandwich configuration. The proposed approach has been successfully implemented for the detection of thrombin in the range of 0.1nM to 1μM. Therefore, the current work has demonstrated enzymatic silver deposition for detection at aptamer-modified electrode. [Copyright &y& Elsevier]