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1.
Cell Biochem Biophys ; 75(2): 185-193, 2017 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-28210984

RESUMO

Spin probe and spin labeling Electron Paramagnetic Resonance methods are indispensable research tools for solving a wide range of bioanalytical problems-from measuring microviscosity and polarity of phase-separated liquids to oxygen concentrations in tissues. One of the emerging uses of spin probes are the studies of proton transfer-related and surface electrostatic phenomena. The latter Electron Paramagnetic Resonance methods rely on molecular probes containing an additional functionality capable of reversible ionization (protonation, in particular) in the immediate proximity to an Electron Paramagnetic Resonance-active reporter group, such as (N-O•) for nitroxides. The consequent formation of protonated and nonprotonated nitroxide species with different magnetic parameters (A iso, g iso) could be readily distinguished by Electron Paramagnetic Resonance. Bioanalytical Electron Paramagnetic Resonance studies employing pH-sensitive paramagnetic probes typically involve determination of the equilibrium constant (pK a) between the protonated and nonprotonated forms of the nitroxide. However, any chemical equilibrium involving charged species, such as ionization of acids and bases, and so the reversible protonation of the nitroxide, is known to be affected by an ionic strength of the solution. Currently, only scarce data for the effect of the solution ionic strength on the experimental pK a's of the ionizable nitroxides can be found in the literature. Here we have carried out a series of Electron Paramagnetic Resonance titration experiments for aqueous solutions of 2,2,3,4,5,5-hexamethylimidazolidin-1-oxyl (HMI) nitroxide known for one of the largest differences in the isotropic nitrogen hyperfine coupling constant A iso between the protonated and nonprotonated forms. Electrolyte concentration was varied over an exceptionally large range (i.e., from 0.05 to 5.0 M) to elucidate the effect of ionic strength on the ionization constant of this pH-sensitive Electron Paramagnetic Resonance probe and the data were compared to the Debye-Hückel limiting law. Effects of the ionic strength on the magnetic parameters of the ionizable nitroxides are also discussed.


Assuntos
Óxidos N-Cíclicos/química , Imidazolidinas/química , Sondas Moleculares/química , Óxidos de Nitrogênio/química , Prótons , Marcadores de Spin , Espectroscopia de Ressonância de Spin Eletrônica , Concentração de Íons de Hidrogênio , Concentração Osmolar , Soluções , Eletricidade Estática , Água/química
2.
Chemphyschem ; 16(6): 1210-6, 2015 Apr 27.
Artigo em Inglês | MEDLINE | ID: mdl-25752503

RESUMO

The organic electrochemical transistor (OECT) is a unique device that shows great promise for sensing in biomedical applications such as monitoring of the integrity of epithelial tissue. It is a label-free sensor that is amenable to low-cost production by roll-to-roll or other printing technologies. Herein, the optimization of a planar OECT for the characterization of barrier tissue is presented. Evaluation of surface coating, gate biocompatibility and performance, and optimization of the geometry of the transistor are highlighted. The conducting polymer poly(3,4-ethylenedioxythiophene):poly(styrene sulfonate), which is used as the active material in the transistor, has the added advantage of allowing significant light transmission compared to traditional electrode materials and thus permits high-quality optical microscopy. The combination of optical and electronic monitoring of cells shown herein provides the opportunity to couple two very complementary techniques to yield a low-cost method for in vitro cell sensing.


Assuntos
Compostos Bicíclicos Heterocíclicos com Pontes/química , Técnicas Eletroquímicas , Células Epiteliais/química , Polímeros/química , Poliestirenos/química , Animais , Compostos Bicíclicos Heterocíclicos com Pontes/metabolismo , Cães , Eletrodos , Células Epiteliais/metabolismo , Células Madin Darby de Rim Canino , Polímeros/metabolismo , Poliestirenos/metabolismo
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