Vesicular Release Dynamics are Altered by Interaction between Chemical Cargo and Vesicle Membrane Lipids

We used liposomes loaded with different monoamines, dopamine (DA) and serotonin (5-HT), to simulate vesicular release and to monitor the dynamics of chemical release from isolated vesicles during vesicle impact electrochemical cytometry (VIEC). The release of DA from liposomes presents a longer release time compared to 5-HT. Modelling the release time showed that DA filled vesicles had a higher percentage of events where the time for the peak fall was better fit to a double exponential (DblExp) decay function, suggesting multiple kinetic steps in the release. By fitting to a desorption-release model, where the transmitters adsorbed to the vesicle membrane, the dissociation rates of DA and 5-HT from liposome membrane were estimated. DA has a lower desorption rate constant, which leads to slower DA release than that observed for 5-HT, whereas there is little difference in pore size. The alteration of vesicular release dynamics due to the interaction between chemical cargo and vesicle membrane lipids provides an important mechanism to regulate vesicular release in chemical and physiological processes. It is highly possible that this introduces a fundamental chemical regulation difference between transmitters during exocytosis.

Vesicular Release Dynamics are Altered by Interaction between Chemical Cargo and Vesicle Membrane Lipids

We used liposomes loaded with different monoamines, dopamine (DA) and serotonin (5-HT), to simulate vesicular release and to monitor the dynamics of chemical release from isolated vesicles during vesicle impact electrochemical cytometry (VIEC). The release of DA from liposomes presents a longer release time compared to 5-HT. Modelling the release time showed that DA filled vesicles had a higher percentage of events where the time for the peak fall was better fit to a double exponential (DblExp) decay function, suggesting multiple kinetic steps in the release. By fitting to a desorption-release model, where the transmitters adsorbed to the vesicle membrane, the dissociation rates of DA and 5-HT from liposome membrane were estimated. DA has a lower desorption rate constant, which leads to slower DA release than that observed for 5-HT, whereas there is little difference in pore size. The alteration of vesicular release dynamics due to the interaction between chemical cargo and vesicle membrane lipids provides an important mechanism to regulate vesicular release in chemical and physiological processes. It is highly possible that this introduces a fundamental chemical regulation difference between transmitters during exocytosis.

EFFECT OF GRAIN SIZE AND ACTIVATION TIME OF ZEOLITE TO ADSORPTION AND DESORPTION OF NH4OH AND KCL AS MODEL OF FERTILIZER-ZEOLITE MIX

- Zeolites can be used as adsorbent, ion exchange, catalyst, or catalyst carrier. Application of fertilizer use in the zeolite also be one of the interesting topic. Zeolites in a mixture of fertilizer can use to control the release of nutrients. The purpose of this research is to study the effect of grain size and time of the activation of zeolite to adsorption and desorption of NH4OH and KCl as modeling of ZA and KCl fertilizer, to obtain the value of adsorption rate constant (ka) and desorption rate constant (kd). This research procedure include: the process of adsorption by adding zeolite with various size and time of activation into a sealed beaker glass and let the adsorption process occurs for 24 hours. After 24 hours, the solution was filtered, the zeolite then put in 100 ml of aquadest into a sealed beaker glass and let the desorption process happened for another 24 hours. Three samples with the largest difference solution concentrations looked for the value of the ka and kd. Zeolite configuration with the largest ka is trialed with fertilizer and compared with the value of ka obtained from modeling. The result for NH4OH adsorbate, -50+60 mesh 2 hours configuration zeolite give the largest ka. For KCl adsorbate, -30+40 mesh 4 hours configuration zeolite give the largest ka. The value between modeling and trials with fertilizers are not much different. Keywords: zeolite, ZA fertilizer, KCl fertilizer, mathematical modelling.

Evaluation of Lagergren Kinetics Equation by Using Novel Kinetics Expression of Sorption of Zn2+ onto Horse Dung Humic Acid (HD-HA)

Extraction and purification of humic acid from dry horse dung powder (HD-HA) was performed successfully and the purified HD-HA was then applied as sorbent to adsorb Zn2+. Extraction and purification were performed based on procedure of Stevenson (1994) under atmospheric air. Parameters investigated in this work consist of effect of medium sorption acidity, sorption rate (ka) and desorption rate constant (kd), Langmuir (monolayer) and Freundlich (multilayer) sorption capacities, and energy (E) of sorption. The ka and kd were determined according to the kinetic model of second order sorption reaching equilibrium, monolayer sorption capacity (b) and energy (E) were determined according to Langmuir isotherm model, and multilayer sorption capacity (B) was determined based on Freundlich isotherm model. Sorption of Zn2+ on purified HD-HA was maximum at pH 5.0. The novel kinetic expression resulted from proposed kinetic model has been shown to be more applicable than the commonly known Lagergren equation obtained from the pseudo-first order sorption model. The application of the equation revealed that the intercept of Lagergren equation, ln qe was more complex function of initial concentration of Zn2+ (a), Langmuir sorption capacity (b), and sorbed Zn2+ at equilibrium (xe).

Desorption rate of glyphosate from goethite as affected by different entering ligands: hints on the desorption mechanism

Environmental contextGlyphosate is a heavily used herbicide that is mobilised in soil and sediments through adsorption–desorption processes from the surface of mineral particles. We demonstrate that the desorption rate of glyphosate from goethite, a ubiquitous mineral, is nearly independent of the concentration and nature of the substance that is used to desorb it. The results elucidate the desorption mechanism and are relevant to understand and predict the environmental mobility of glyphosate. AbstractThe desorption kinetics of glyphosate (Gly) from goethite was studied in a flow cell using attenuated total reflectance Fourier-transform infrared spectroscopy. Because Gly forms an inner-sphere surface complex by coordinating to Fe atoms at the goethite surface, the desorption process is actually a ligand-exchange reaction, where Gly is the leaving ligand and water molecules or dissolved substances are the entering ligands. A series of possible entering ligands that can be found in nature was tested to evaluate their effect on the desorption kinetics of Gly. Contrarily to expectations, the desorption rate was quite independent of the entering ligand concentration. Moreover, the identity of this ligand (phosphate, citrate, sulfate, oxalate, EDTA, thiocyanate, humic acid, water) had only a small effect on the value of the desorption rate constant. By analogy with the reactivity of transition metal complexes in solution, it is concluded that the rate is mainly controlled by the breaking of the Fe–Gly bond, through a dissociative or a dissociative interchange mechanism. The results are relevant in understanding and predicting the environmental mobility of Gly: irrespective of the identity of the entering ligand, Gly will always desorb from iron (hydr)oxides in nature at nearly the same rate, simplifying calculations and predictions enormously. The importance of studying desorption kinetics using mineral surfaces and environmentally relevant molecules is also highlighted.

Shear-Induced Lift Force on a Single Bubble in Surfactant Solutions

In this paper, single bubble motion in surfactant solutions is discussed. We focus on the change of the shear-induced lift force acting on a bubble when the bubble surface is contaminated by surfactant adsorption which leads the Marangoni effect. With the increase of Langmuir number corresponding to the decrease of desorption rate constant of surfactant, the lift force on a spherical bubble decreases from that on a clean bubble to near zero value. This reduction is related significantly to the asymmetry of pressure distribution on surface. Comparing the present result with our previous simulation using the stagnant cap model, the lift force of this study is larger than that of the stagnant cap model. This is because in a shear flow, the surface concentration distributes asymmetrically, and the asymmetry of the surface pressure produced by the shear appears stronger than that of the stagnant cap model.

Adsorption and Desorption of Contaminant Metals on Si Wafer Surface in SC1 Solution

ABSTRACTVariation in the surface concentration of Fe, Ni, Cu and Zn on Si wafers due to treatment in NH4OH/H2aO2/H2O solution called SC1 is investigated. The metal concentration on the wafer surface depends on the initial surface concentration, concentration in the solution, adsorption probability, desorption rate constant and the treatment time. The surface metal concentration behavior is explained by taking into account the effects of these parameters. The variation in the desorption rate constant with the metal species, the concentration in the solution, treatment temperature and mixing ratio of SC1 is discussed.