We present here the detection of dopamine (DA) at nanopipet electrodes with radii of hundreds of nanometers ranging from 160 nm to 480 nm. Dibenzo-18-crown-6 (DB18C6) was employed as an ionophore to facilitate DA transfer, resulting in a half-wave transfer potential, E, of -0.322 (±0.020) V vs. E. Well-defined steady-state sigmoidal cyclic voltammograms were observed for the transfer of DA. High resolution scanning electron microscopy was used to measure the size and taper angle of the nanopipet electrodes. The detection is linear with concentration of DA ranging from 0.25 mM to 2 mM; calculated diffusion coefficient at nanopipet electrodes with above mentioned sizes is 4.87 (±0.28) 10 m/s. The effect of the common interferent ascorbic acid on DA detection with nanopipet electrodes was evaluated, where DA detection still shows linear behavior with well-defined sigmoidal CVs with E being -0.328 (±0.029) V vs. E. The diffusion coefficient for DA transfer in MgCl with the presence of 2 mM AA was measured to be 1.93 (±0.59) 10 m/s on nanoelectrodes with radii from 161 nm to 263 nm, but the physiological concentration of 0.1 mM AA had no effect on DA's diffusion coefficient.
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http://dx.doi.org/10.1149/2.0091604jes | DOI Listing |
Anal Chem
September 2020
Department of Chemistry, University of Warwick, Coventry CV4 7AL, United Kingdom.
Electrochemical impedance spectroscopy (EIS) is a versatile tool for electrochemistry, particularly when applied locally to reveal the properties and dynamics of heterogeneous interfaces. A new method to generate local electrochemical impedance spectra is outlined, by applying a harmonic bias between a quasi-reference counter electrode (QRCE) placed in a nanopipet tip of a scanning ion conductance microscope (SICM) and a conductive (working electrode) substrate (two-electrode setup). The AC frequency can be tuned so that the magnitude of the impedance is sensitive to the tip-to-substrate distance, whereas the phase angle is broadly defined by the local capacitive response of the electrical double layer (EDL) of the working electrode.
View Article and Find Full Text PDFAnal Chem
October 2019
Department of Chemistry and Biochemistry , Queens College, Flushing , New York 11367 , United States.
Carbon fiber micro- and nanoelectrodes have been extensively used to measure dopamine and other neurotransmitters in biological systems. Although the radii of some reported probes were ≪1 μm, the lengths of the exposed carbon were typically on the micrometer scale, thus limiting the spatial resolution of electroanalytical measurements. Recent attempts to determine neurotransmitters in single cells and vesicles have provided additional impetus for decreasing the probe dimensions.
View Article and Find Full Text PDFAnal Chem
February 2019
Department of Chemistry , The University of Rhode Island, Kingston , Rhode Island 02881 , United States.
Effective delivery and accumulation of antimicrobial agents into the microbial organism is essential for the treatment of bacterial infections. Transports of hydrophilic drug molecules, however, encounter a robust barrier of hydrophobic double membrane cell envelope, thus, leading to drug-resistance in Gram-negative bacteria. Accordingly, a deeper understanding about a transit of charged molecules through a bacterial membrane is needed to remediate the antibacterial resistance.
View Article and Find Full Text PDFAnal Chem
December 2018
Department of Chemistry , University of Washington, Seattle , Washington 98195-1700 , United States.
We report the use of a Pt bipolar electrochemical nanocell and fluorescence to detect single redox molecules. A Pt nanocell is formed by depositing a Pt particle at a nanopipet orifice which separates the inside pipet volume from the bulk solution. Highly fluorescent resorufin molecules are generated on the inner Pt surface and optically detected and counted due to unique properties of the nanocell.
View Article and Find Full Text PDFAnal Chem
December 2018
Department of Chemistry , Imperial College London, Exhibition Road , London SW7 2AZ , United Kingdom.
By combining DNA nanotechnology and high-bandwidth single-molecule detection in nanopipets, we demonstrate an electric, label-free hybridization sensor for short DNA sequences (<100 nucleotides). Such short fragments are known to occur as circulating cell-free DNA in various bodily fluids, such as blood plasma and saliva, and have been identified as disease markers for cancer and infectious diseases. To this end, we use as a model system an 88-mer target from the RV1910c gene in Mycobacterium tuberculosis, which is associated with antibiotic (isoniazid) resistance in TB.
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