Ionic Exchanges of Poly-(Azure A) Studied by AC-Electrogravimetry

2011 ◽  
Keyword(s):  
Azure A ◽  
2019 ◽  
Vol 35 (10) ◽  
pp. 43-51
Author(s):  
Jerónimo Agrisuelas ◽  
Claude Gabrielli ◽  
José Juan García-Jareño ◽  
Hubert Perrot ◽  
Francisco Vicente
Keyword(s):  
Azure A ◽  

Toxicology ◽  
2021 ◽  
Vol 455 ◽  
pp. 152766
Author(s):  
Byanca Thais Lima de Souza ◽  
Eduardo Makiyama Klosowski ◽  
Márcio Shigueaki Mito ◽  
Renato Polimeni Constantin ◽  
Gislaine Cristiane Mantovanelli ◽  
...  

2019 ◽  
Vol 298 ◽  
pp. 126878 ◽  
Author(s):  
Rebeca Jiménez-Pérez ◽  
José González-Rodríguez ◽  
María-Isabel González-Sánchez ◽  
Beatriz Gómez-Monedero ◽  
Edelmira Valero

2007 ◽  
Vol 111 (38) ◽  
pp. 14230-14237 ◽  
Author(s):  
J. Agrisuelas ◽  
C. Gabrielli ◽  
J. J. García-Jareño ◽  
D. Giménez-Romero ◽  
H. Perrot ◽  
...  

1965 ◽  
Vol s3-106 (76) ◽  
pp. 299-306
Author(s):  
D. J. GOLDSTEIN

If two histological sections, of thickness nµ and 2nµ, and having the same apparent intensity of staining, are at equilibrium with dyebaths of concentration B1 and B2 respectively, the affinity of the histological substrate for the dye is, under denned conditions, given by the expression ΔF° = - RT In I/B, where B is either (i) B2 if the thinner section is stained to saturation, or (ii) B1 if B1 = 3B2. The affinity tends to be greater when measured in a weaker dyebath, as implied in method (ii). Evidence is presented suggesting that the uptake of the basic dye Azure A by pancreatic basal chromidial substance, goblet cell mucin and intestinal epithelial cytoplasm follows a Langmuir adsorption isotherm to a first approximation, in that, at low dyebath concentrations, the uptake of dye is proportional to the concentration of dyebath with which the substrate is in equilibrium, while in strong dyebaths the uptake approaches a plateau. A deviation from the ideal Langmuir isotherm in dyebaths of moderate concentration, observed in epithelial cytoplasm and to a lesser extent in pancreatic basal chromidial substance, may have been due to interaction between neighbouring dye-binding sites, or to the presence in a single area of sites with different affinities for the dye.


1988 ◽  
Vol 136 (1) ◽  
pp. 461-481 ◽  
Author(s):  
CHRIS M. WOOD

Unidirectional Na+ and Cl− fluxes, net fluxes of Na+, Cl−, other ions, titratable acid (TA), ammonia and acidic equivalents (net H+) across the gills, together with the comparable renal fluxes, were monitored throughout a 24-h period after exhaustive exercise (simple chasing) in the rainbow trout. The gills were the major site of flux. The renal excretion of [TA-HCO3−], ammonia, lactate and most electrolytes increased after exercise, coincident with diuresis. Relative to the gills, the kidney accounted for only 8% of net H+ flux, 0–15% of net electrolyte losses and 50% of lactate loss, though the latter was negligibly small. Approximately 1000 μequiv kg−1 of net H+ were transported across the gills to the water during the first 4h, and then fully recovered over the subsequent 8h, coincident with periods of extracellular acidosis and alkalosis recorded in previous studies. Ammonia efflux increased during the first 4h; changes in titratable acid flux and extracellular PNHNH3 and NH4+ levels suggest that this elevation occurred partially as NH3 diffusion in the first hour, and thereafter mainly as NH4+ exchange. Small net Na+ losses (≊300 μequivkg−1), moderate net K+ losses (≊600 μequiv kg−1) and large net Cl− losses (≊1200 μequiv kg−1) correlated well with previously reported plasma changes; only the Na+ deficit was fully corrected by 24 h. Na+ influx was stimulated and Cl− influx inhibited during the 0–4 h period of net H+ excretion, whereas Na+ influx returned to control levels and Cl− influx increased during the 4–12 h period of net H+ uptake. These data indicate dynamic modulation of Na+/NH4+,H+ and C1−/HCO3−,OH− exchanges; however, an excess of Cl− over Na+ efflux also contributed to net H+ excretion. Acidic equivalent flux correlated well with [Na+-Cl−] net flux, in accord with strong ion difference theory.


1977 ◽  
Vol 55 (5) ◽  
pp. 1179-1189 ◽  
Author(s):  
Louis B. Jaques ◽  
Tak K. Sue ◽  
Norman M. McDuffie ◽  
Sandra M. Wice

Heparin (Hep), hyaluronic acid, chondroitins (sulfate) A, B, and C, and heparitins (sulfate) A, B, C, and D were subjected to microelectrophoresis in barbital–agarose gel, fixed with cetylpyridinium chloride and stained with toluidine blue. The optical densities of the resulting bands were compared with optical densities obtained upon reaction with azure A in aqueous solution and with the carbazole reagent. A linear relation was obtained between optical density and concentration of purified sulfated mucopolysaccharide (SMP). Less than 1 μg of Hep and 2 μg of other SMPs are required for measurement by electrophoresis, while about 30 μg of each is required with the carbazole reagent. The optical density of a mixture of SMPs was equal to the sum of the densities for the individual SMPs upon microelectrophoresis. It was demonstrated that the individual SMPs in mixtures were distinguished by reaction with specific enzymes and by changes in migration in agarose with barbital, phthalate, ethylenediamine, or propane-diamine buffers, permitting ready demonstration and quantitation of various SMP species. Examples are shown of the application of the procedure to measure the total SMPs and individual SMPs in tissue extracts. The method is sensitive, reproducible, flexible, and measures quantities [Formula: see text] of those measured colorimetrically, yet is relatively unaffected by protein, carbohydrate, or inorganic electrolytes.


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