20 research outputs found
Backside calibration chronopotentiometry: using current to perform ion measurements by zeroing the transmembrane ion flux
A recent new direction in ion-selective electrode (ISE) research utilizes a stir effect to indicate the disappearance of an ion concentration gradient across a thin ion-selective membrane. This zeroing experiment allows one to evaluate the equilibrium relationship between front and backsidesolutions contacting the membrane by varying the backside solution composition. This method is attractive since the absolute potential during the measurement is not required, thus avoiding standard recalibrations from the sample solution and a careful control of the reference electrode potential. We report here on a new concept to alleviate the need to continuously vary the composition of the backside solution. Instead, transmembrane ion fluxes are counterbalanced at an imposed critical current.A theoretical model illustrates the relationship between the magnitude of this critical current and the concentration of analyte and countertransporting ions and is found to correspond well with experimental results. The approach is demonstrated with lead(II)-selective membranes and protons as dominating interference ions, and the concentration of Pb2+ was successfully measured in tap water samples. The principle was further evaluated with calcium-selective membranes and magnesium as counterdiffusing species, with good results. Advantages and limitations arising from the kinetic nature of the perturbation technique are discussed
Polymerized Nile Blue Derivatives for Plasticizer-Free Fluorescent Bulk Optode Ion Sensors
Backside Calibration Chronopotentiometry: Using Current to Perform Ion Measurements by Zeroing the Transmembrane Ion Flux
Studies on the Sorption of Cadmium(II), Zinc(II), and Copper(II) with PTFE Selective Resin Containing Primary Amine N1923 and Cyanex923
Direct Ion Speciation Analysis with Ion-Selective Membranes Operated in a Sequential Potentiometric/Time Resolved Chronopotentiometric Sensing Mode
Immobilization of Functional Materials onto Poly(styrene-co-divinylbenzene) Gels by Gamma Irradiation and Adsorption Properties
A Sensitive Method for Determination Glycolic Acid, Mono- and Di-Chloroacetic Acids in Betaine Media Using Amino-Functionalized SBA-15 as a Sorbent and HPLC Assay
Solid phase extraction of chromium(VI) using Aliquat336 immobilized on a thin film of multiwall carbon nanotubes
Nile Blue-Based Nanosized pH Sensors for Simultaneous Far-Red and Near-Infrared Live Bioimaging
Diblock copolymer vesicles are tagged with pHresponsive
Nile Blue-based labels and used as a new type of
pH-responsive colorimetric/fluorescent biosensor for far-red
and near-infrared imaging of live cells. The diblock copolymer
vesicles described herein are based on poly(2-
(methacryloyloxy)ethyl phosphorylcholine-block-2-
(diisopropylamino)ethyl methacrylate) [PMPC-PDPA]: the
biomimetic PMPC block is known to facilitate rapid cell
uptake for a wide range of cell lines, while the PDPA block
constitutes the pH-responsive component that enables facile vesicle self-assembly in aqueous solution. These biocompatible
vesicles can be utilized to detect interstitial hypoxic/acidic regions in a tumor model via a pH-dependent colorimetric shift. In
addition, they are also useful for selective intracellular staining of lysosomes and early endosomes via subtle changes in
fluorescence emission. Such nanoparticles combine efficient cellular uptake with a pH-responsive Nile Blue dye label to produce
a highly versatile dual capability probe. This is in marked contrast to small molecule dyes, which are usually poorly uptaken by
cells, frequently exhibit cytotoxicity, and are characterized by intracellular distributions invariably dictated by their hydrophilic/
hydrophobic balance